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ASPARAGUS (ALK-Abello, Inc.)

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INJECTION, SOLUTION 5 mL in 1 VIAL, MULTI-DOSE (0268-6103-06) Label Information

Complete ASPARAGUS Information

  • BOXED WARNING(What is this?)

    WARNINGS

    This product is intended for use by physicians who are experienced in the administration of allergenic extracts and the emergency care of anaphylaxis, or for use under the guidance of an allergy specialist.

    As with all allergenic extracts, severe systemic reactions may occur. In certain individuals these life-threatening reactions may result in death. Fatalities associated with skin testing have been reported. Patients should be observed for at least 20 - 30 minutes following testing. Emergency measures and adequately trained personnel should be immediately available in the event of a life-threatening reaction.

    Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction.

    Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and/or death. Adverse events are to be reported to MedWatch (1-800-FDA-1088), Adverse Experience Reporting, HFM-210 Center for Biologics Evaluation & Research, Food and Drug Administration, 1401 Rockville Pike, Rockville, MD 20852-1448.

    This product should not be injected intravenously. Patients receiving beta blockers may not be responsive to epinephrine or inhaled bronchodilators. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require theophylline, oxygen, intubation and the use of life support systems. Parenteral fluid and/or plasma expanders may be utilized for the treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously.

    Refer to WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS sections below.

                     

     


  • SPL UNCLASSIFIED SECTION

    ALLERGENIC EXTRACTS, FOR DIAGNOSTIC USE ONLY

    DIRECTIONS FOR USE


  • DESCRIPTION

    Sterile diagnostic extracts are supplied in either phenol-saline diluent for Intradermal Testing or in diluent containing glycerin 50% (v/v) for Percutaneous Testing and phenol 0.4% (preservative). Inactive ingredients may include: sodium chloride for isotonicity, glycerin, and sodium bicarbonate as a buffer. Inactive ingredients in mold extracts may include residual potassium phosphate, and calcium carbonate from growth media.

    Pollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and after final packaging, they are tested for sterility and safety.

    House Dust, a heterogenous, widely distributed allergen, is among the most frequently encountered as a primary or accompanying cause of allergic symptoms. Allergic inhalants found in house dust include mites, insects, mold spores, feathers, animal dander, pollens, hairs, food and cleansing agent residues. Individual environs may contain certain items not ordinarily found so that a stock house dust extract may not elicit a response on testing. House Dust Extracts are prepared from dust collected from homes and from establishments which clean household rugs. It is extracted from buffered, aqueous extracting fluid. House Dust Extract is dialyzed, filtered aseptically, and after final packaging is tested for sterility and safety.

    Molds (fungi) are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously. Mold extracts are extracted in a phenol preserved saline solution. The extract is dialyzed, filtered aseptically and after final packaging is tested for sterility and safety.

    Foods, miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline, filtered aseptically and after final packaging are tested for sterility and safety.


  • CLINICAL PHARMACOLOGY

    Diagnostically (for skin testing), the allergen combines with IgE antibodies fixed to mast cells in the skin. This complexing causes an increase in cellular permeability and degranulation of the mast cells releasing chemical mediators. These mediators (such as histamine) are responsible for a local inflammatory response of wheal and erythema typical of a positive skin test reaction and also, the symptoms commonly associated with allergic disease.1 The more mediator release, the larger the reaction (wheal and erythema).


  • INDICATIONS AND USAGE

    These products are for diagnostic use only. Diagnostic allergenic extracts are indicated for use in skin testing to establish the clinical relevance of specific allergens to which the patient has been exposed. By measuring skin test response the physician may assess the degree of sensitivity that patients have to the allergens. For extracts standardized in AU and BAU, see individual directions for use.  Allergenic extracts for diagnostic use only of coffee, mosquito, cottonseed, and flaxseed have not been shown by adequate data to be safe and effective for therapeutic use.


  • CONTRAINDICATIONS

    Patients on beta blockers can be non-responsive to beta agonists that may be required to reverse a systemic reaction (also, see boxed WARNINGS statement and ADVERSE REACTIONS). The physician should carefully weigh the benefit derived from skin testing vs. the risk to the patient should a systemic reaction arise.

    Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction2, 3. See also PRECAUTIONS and ADVERSE REACTIONS.


  • WARNINGS

    Patients should always be observed for at least 20 - 30 minutes after skin testing. In the event of a marked systemic reaction such as urticaria, angioedema, wheezing, dyspnea, respiratory obstruction, hypotension, coma and death (see ADVERSE REACTIONS), applications of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of epinephrine injection (1:1,000) are recommended. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet is then gradually released at 15 minute intervals. Patients under treatment with beta blockers may be refractory to the usual dose of epinephrine.

    Volume expanders and vasopressor agents may be required to reverse hypotension, inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In case of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reactions unresponsive to the above may require cardiopulmonary resuscitation.


  • PRECAUTIONS

    INFORMATION FOR PATIENTS:

    Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to testing. Also, see ADVERSE REACTIONS and WARNINGS Sections.

    Patients should always be observed 20 to 30 minutes after testing.

    General:

    1. In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indications for skin testing must be weighed carefully against the risk of temporarily aggravating the symptoms by the testing itself. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration and prior to discharge may be useful in unstable asthmatics to reduce the chances of exacerbation of the patient’s asthma. Patients should be instructed to describe any active allergic symptoms as described above prior to skin testing and encouraged to report any late reactions from this testing. Also, see ADVERSE REACTIONS and WARNINGS sections.
    2. Store allergenic extracts between 2o - 8o C at all times, even during use.
    3. Care must be taken to avoid drawing blood.
      1. For percutaneous testing, if blood is observed, immediately wipe the allergen from the site.
      2. For intradermal skin testing, pull gently on the syringe plunger and note if any blood enters the syringe. If blood is obtained, reposition the needle and repeat before injecting (see DOSAGE AND ADMINISTRATION).

    4. Allergenic extracts become less potent with age. Allergenic extracts containing glycerin 50% v/v are relatively stable. Non-glycerinated aqueous extracts, particularly dilute forms as used for intradermal skin testing, have been shown to be extremely unstable. Until such time as stability studies are complete with dilute allergens, new intradermal strength materials should be prepared every few weeks.
    5. Use standard aseptic precautions if making dilutions from stock concentrates to intradermal strength.
    6. For intradermal testing: Extracts in glycerin 50% v/v must be diluted with a non-glycerinated diluent and must be diluted at least 25-fold to less than 2% glycerin by volume, as glycerin above this level can cause false positive intradermal skin test results.

    PREGNANCY - CATEGORY C:

    Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.

    Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother4. However, on the basis of histamine's known ability to contract the uterine muscle, the release of significant amounts of histamine from allergen exposure to skin test overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.

    Pediatric Use:

    Allergenic extracts for diagnostic use have been given safely in infants and young children. Infants have lower skin test reactivity to histamine, as well as common allergens. Skin test reactivity gradually increases to age 6 and plateaus to age 60. Therefore, small skin test reactions should be anticipated in children under age 6.

    Geriatric Use:

    Skin test reactivity gradually decreases after age 60. Therefore, smaller skin test reactions should be anticipated in adults over age 60.

    Nursing Mothers:

    It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

    Carcinogenesis, mutagenesis, impairment of fertility:

    Studies in animals have not been performed.

    Drug Interactions:

    Drugs can interfere with the performance of skin tests5.

    Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine), and can be as long as 40 days (astemizole).

          Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.

          Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.

          Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.

          Beta Blocking Agents: Propanolol can significantly increase skin test reactivity.

          Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.


  • ADVERSE REACTIONS

    Fatalities from skin testing in the United States have been extensively reviewed by Lockey.2 Six fatalities were associated with intradermal testing without previous percutaneous testing and one was associated with a combination of percutaneous (scratch) and intradermal skin testing. With careful attention to dosage and administration, fatal reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and overdosage could result in anaphylactic symptoms. Therefore it is imperative that physicians administering allergenic extracts for skin testing understand, and be prepared for the treatment of severe reactions.

    Local: Immediate wheal and erythema reactions are to be expected; but if very large, may be the first manifestation of a systemic reaction. In such cases, immediately wipe the test site(s) with sterile gauze or cotton to remove excess allergen.

    Systemic Reactions: Systemic reactions are characterized by one or more of the following symptoms: sneezing, mild to severe generalized urticaria, itching (other than at the skin test site), extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, hypotension, syncope, and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 - 30 minutes after testing.

    Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction unresponsive to bronchodilator may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.02 mL to 1.0 mL of epinephrine injection (1:1,000) is recommended. Maximum recommended dose for children between 2 and 12 years of age is 0.3 mL. The tourniquet should not be left in place without loosening for 90 seconds every 15 minutes.

    Adverse events should be reported via MedWatch (1-800-FDA-1088). Adverse experience Reporting, HFM-210 Center for Biologics Evaluation & Research, Food and Drug Administration, 1401 Rockville Pike, Rockville, MD 20852-1448.


  • OVERDOSAGE

    Signs and symptoms of overdose are typically large local and systemic reactions. For management of overdose reactions, refer to the ADVERSE REACTIONS section above.


  • DOSAGE AND ADMINISTRATION

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    Skin test techniques for immediate (Type I) hypersensitivity testing fall into two major categories: percutaneous, and intracutaneous.

    Percutaneous techniques: For percutaneous testing, in general, skin is scratched, punctured or pricked just before the allergen is applied or through a drop of test allergen. There are several devices available for this technique. Refer to the manufacturer or distributor's circular for specific directions for their use.

    In General:

    1. It is recommended that the test areas should be placed no closer than 4 - 5 cm apart to avoid interference of reactions when several tests are applied.
    2. Skin test areas should be cleansed with alcohol and air dried.
    3. Preferably, the allergen should be placed on the volar surface of the forearm, upper arm, or the patient's back. The patient should be placed in a comfortable position prior to testing.
    4. For scratch testing, a sharp, clean, sterile instrument is used to abrade the skin, but not to draw blood. Each scratch should be about 2 - 4 mm in length. A small drop of extract is placed on the surface of the skin.
    5. Prick testing: For prick testing, a sharp, sterile instrument is used to puncture the skin slightly, applying it at a 15 - 20o angle to the skin. The instrument is gently raised, "tenting” the skin until it pops out, generally pricking through the drop of allergen. Do not draw blood.
    6. For puncture testing, a sharp, clean, sterile instrument must be used. Puncture the skin, through the drop of allergen, perpendicular to the skin. Do not draw blood.

    For all of the above techniques, a separate instrument must be used for each patient; if the instrument is to be used to pass through the allergen, to avoid cross-contamination, a separate instrument is to be used for each allergen. The test should be read in 15 minutes, measuring both wheal size and erythema.

    Intracutaneous (intradermal) testing: General: Intradermal testing is more sensitive than percutaneous testing and its specificity is dependent on dose. Intradermal testing is not intended as an initial screen unless used in highly dilute solutions. Intradermal testing is usually reserved for allergens that have demonstrated either negative or equivocal percutaneous skin test response in the face of positive or unclear history.

    Intradermal testing of one allergen in several serial dilutions (beginning with the weakest to the more concentrated dilutions) may also be useful in assessing degree of patient sensitivity for the establishment of a safe starting dose for immunotherapy.

    Bulk extracts must be diluted for intradermal testing. Use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly, 10 fold dilutions are used to achieve a desired concentration for intradermal testing and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of diluent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration. As a general rule intradermal strength should begin at no higher than 1/100 to 1/1000 of the percutaneous strength that resulted in a negative skin test reaction.

    1. It is recommended that the test areas should be spaced no less than 5 cm apart to avoid interference with adjacent allergen or control.
    2. Skin should be cleansed with alcohol and air dried.
    3. A sterile 1 mL or ½ mL syringe with a 26 - 30 gauge needle should be used. A separate sterile syringe should be used for each extract and each patient.
    4. Care should be taken to eliminate air bubbles from the syringe prior to injecting the test dose. It is suggested that not more than 6 - 10 allergens of each different type be used at any one time. Very sensitive patients may show rapid response.
    5. The skin is held tensely, and the needle is inserted almost parallel to the skin, beveled side up far enough to cover the beveled portion. Slowly inject sufficient extract to make a small bleb of approximately 5 mm in diameter (0.01 - 0.02 mL).
    6. Read the test results in 15 minutes.

    Selection of the proper strength for intracutaneous testing: A general rule for the prevention of untoward reactions, particularly in extremely sensitive patients, is to screen by percutaneous methods initially, and begin intradermal testing at a strength not more than 1/100 of a negative or equivocal percutaneous reaction.

    Controls: In both percutaneous and intracutaneous tests, a negative control test with diluent alone should be performed because some patients exhibit dermographia, and/or other non-specific irritant responses.

    As a positive control in the evaluation of allergenic skin testing, histamine 1 mg/mL (histamine base) should be used for percutaneous testing, and histamine 0.1 mg/mL (histamine base) should be used for intradermal testing.

    Interpretation of results: Patient's response is graded on the basis of the size of erythema or wheal.6 General guidelines follow for percutaneous testing, different devices and/or techniques influence the size of the reaction, therefore it is important to refer to the device manufacturer's or distributor's instructions when grading reactions.

    Percutaneous (prick or scratch) test:

    0 No reaction or less than control.
    + Erythema greater than control, smaller than a nickel (21 mm diameter).
    ++ Erythema greater than a nickel in diameter, no wheal.
    +++ Wheal and erythema without pseudopods.
    ++++ Wheal and erythema with pseudopods.

    Intradermal test:

    0 No reaction or less than negative control.
    + 3-4 mm wheal with erythema, or erythema alone larger than a nickel (21 mm diamether).
    ++ 4-8 mm wheal and erythema, without pseudopods.
    +++ Over 8 mm wheal and erythema without pseudopods
    ++++ Wheal and erythema with pseudopods.

  • HOW SUPPLIED

    For scratch and prick testing: 5 mL dropper applicator vials in 50% v/v glycerin. Available individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

    For intracutaneous testing: 5 mL sterile vials, aqueous based, individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

    HistatrolR Positive skin test control - histamine. 1 mg/mL and 0.1 mg/mL histamine base.

    See Product Catalog for specific diagnostic concentrations available.


  • STORAGE

    To maintain stability of allergenic extracts, proper storage conditions are essential. Bulk concentrates and diluted extracts are to be stored at 2o to 8o C even during use. Bulk or diluted extracts are not to be frozen. Do not use after the expiration date shown on the vial label.


  • REFERENCES

    1. Holgate, S.T., Robinson, C. and Church, M.K., Mediators of immediate hypersensitivity. In Middleton et al: Allergy Principles and Practice, St. Louis, 1988, C.V. Mosby, p 135.
    2. Lockey, R.F., et al, Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol., 1987:79:660.
    3. Reid, M.J. et al.  Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin Immunol. 1993; 92:6.
    4. DeBuske L. M. et al.  Special problems regarding Allergen Immunotherapy in Immunology and Allergy Clinics of North America. Greenburger, P.A. Ed. February 1992; 145-149.
    5. Bousquet, J. In vivo methods for the study of allergy: skin test, techniques and interpretation. In: Middleton et al.: Allergy Principles and Practice 3rd Ed. St. Louis: DV Mosby, 1988:167.
    6. Freedman, S.O., Asthma and Allergic Rhinitis II. Clinical Aspects, in Freedman and Gold Clinical Immunology 2nd Ed. New York: Harper & Row, 1976:131.

    Revision: June 2002

    ©ALK-Abello, Inc.                                                 112N

    Distributed in Canada by:

    Western Allergy Services, LTD.

    121-6154 Westminister Highway

    Richmond, B.C. V7C404


  • PRINCIPAL DISPLAY PANEL

    ALLERGENIC EXTRACT
    DIN 00299979
    5mL sterile multiple dose vial
    FOR PERCUTANEOUS TESTING ONLY

    PRINCIPAL DISPLAY PANEL
ALLERGENIC EXTRACT
DIN 00299979
5mL sterile multiple dose vial
FOR PERCUTANEOUS TESTING ONLY


  • INGREDIENTS AND APPEARANCE
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    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6000
    Route of Administration PERCUTANEOUS
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    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6000-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
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    Route of Administration PERCUTANEOUS
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    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6100-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
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    Route of Administration PERCUTANEOUS
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    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
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    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
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    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6101-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
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    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
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    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6102-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
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    Route of Administration PERCUTANEOUS
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    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6103-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
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    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6104-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
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    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BANANA (UNII: 4AJZ4765R9) (BANANA - UNII:4AJZ4765R9) BANANA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6105-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BARLEY 
    barley food injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6106
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BARLEY (UNII: 5PWM7YLI7R) (BARLEY - UNII:5PWM7YLI7R) BARLEY 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6106-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BEAN 
    pinto bean kidney bean injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6107
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BEAN (UNII: 8WB9PV3YW5) (BEAN - UNII:8WB9PV3YW5) BEAN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6107-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STRING BEAN 
    string bean green bean injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6108
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STRING BEAN (UNII: N9D69B2Q7Y) (STRING BEAN - UNII:N9D69B2Q7Y) STRING BEAN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6108-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BEEF 
    beef injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6109
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BEEF (UNII: 4PIB2155QP) (BEEF - UNII:4PIB2155QP) BEEF 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6109-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BRAZIL NUT 
    brazil nut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6110
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BRAZIL NUT (UNII: XKR79OET1K) (BRAZIL NUT - UNII:XKR79OET1K) BRAZIL NUT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6110-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BROCCOLI 
    broccoli injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6112
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BROCCOLI (UNII: UOI4FT57BZ) (BROCCOLI - UNII:UOI4FT57BZ) BROCCOLI 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6112-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BUCKWHEAT 
    buckwheat injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6113
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3) BUCKWHEAT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6113-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CABBAGE 
    cabbage injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6114
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CABBAGE (UNII: GW0W1Y9I97) (CABBAGE - UNII:GW0W1Y9I97) CABBAGE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6114-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANTALOUPE 
    cantaloupe injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6115
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANTALOUPE (UNII: 8QF5D5H6UH) (CANTALOUPE - UNII:8QF5D5H6UH) CANTALOUPE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6115-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CARROT 
    carrot injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6116
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARROT (UNII: L56Z1JK48B) (CARROT - UNII:L56Z1JK48B) CARROT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6116-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CASEIN 
    casein injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6118
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CASEIN (UNII: 48268V50D5) (CASEIN - UNII:48268V50D5) CASEIN 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6118-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CELERY 
    celery injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6120
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CELERY (UNII: 44IDY6DTKX) (CELERY - UNII:44IDY6DTKX) CELERY 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6120-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHERRY 
    cherry injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6121
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHERRY (UNII: BUC5I9595W) (CHERRY - UNII:BUC5I9595W) CHERRY 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6121-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHICKEN 
    chicken meat injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6122
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHICKEN (UNII: 0X8Q245Y7B) (CHICKEN - UNII:0X8Q245Y7B) CHICKEN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6122-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CINNAMON 
    cinnamon injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6123
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB) CINNAMON 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6123-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLAM 
    clam injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6124
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUAHOG, UNSPECIFIED (UNII: 226LY0AFR9) (QUAHOG, UNSPECIFIED - UNII:226LY0AFR9) QUAHOG, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6124-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCOA BEAN 
    cocoa bean whole bean chocolate injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6125
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCOA (UNII: D9108TZ9KG) (COCOA - UNII:D9108TZ9KG) COCOA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6125-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCONUT 
    coconut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6127
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCONUT (UNII: 3RT3536DHY) (COCONUT - UNII:3RT3536DHY) COCONUT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6127-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CODFISH 
    codfish injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6128
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COD, UNSPECIFIED (UNII: 8D6Q5LNG3D) (COD, UNSPECIFIED - UNII:8D6Q5LNG3D) COD, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6128-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COFFEE BEAN 
    coffee injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6129
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COFFEE BEAN (UNII: JFH385Y744) (COFFEE BEAN - UNII:JFH385Y744) COFFEE BEAN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6129-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CRAB 
    crab leg, unspecified injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6130
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CRAB LEG, UNSPECIFIED (UNII: S1VF61QLO9) (CRAB LEG, UNSPECIFIED - UNII:S1VF61QLO9) CRAB LEG, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6130-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CUCUMBER 
    cucumber injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6132
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CUCUMBER (UNII: YY7C30VXJT) (CUCUMBER - UNII:YY7C30VXJT) CUCUMBER 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6132-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EGG WHITE 
    egg white injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6133
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EGG WHITE (UNII: 3E0I92Z2GR) (EGG WHITE - UNII:3E0I92Z2GR) EGG WHITE 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6133-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EGG 
    whole egg injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6135
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EGG (UNII: 291P45F896) (EGG - UNII:291P45F896) EGG 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6135-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EGG YOLK 
    egg yolk injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6136
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EGG YOLK (UNII: 4IPS17B70T) (EGG YOLK - UNII:4IPS17B70T) EGG YOLK 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6136-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FLOUNDER 
    flounder injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6137
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FLOUNDER, UNSPECIFIED (UNII: T197LO581X) (FLOUNDER, UNSPECIFIED - UNII:T197LO581X) FLOUNDER, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6137-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    GARLIC 
    garlic injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6138
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GARLIC (UNII: V1V998DC17) (GARLIC - UNII:V1V998DC17) GARLIC 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6138-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    GRAPE 
    white seedless grape injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6139
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GRAPE (UNII: 6X543N684K) (GRAPE - UNII:6X543N684K) GRAPE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6139-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    GRAPEFRUIT 
    grapefruit injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6141
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GRAPEFRUIT (UNII: O82C39RR8C) (GRAPEFRUIT - UNII:O82C39RR8C) GRAPEFRUIT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6141-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    KARAYA GUM 
    karaya gum bassora injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6143
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KARAYA GUM (UNII: 73W9IQY50Q) (KARAYA GUM - UNII:73W9IQY50Q) KARAYA GUM 0.005 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6143-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    HONEYDEW MELON 
    honeydew injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6146
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HONEYDEW MELON (UNII: RN8P45F92A) (HONEYDEW MELON - UNII:RN8P45F92A) HONEYDEW MELON 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6146-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    LAMB 
    lamb injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6149
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LAMB (UNII: FOF26T73HA) (LAMB - UNII:FOF26T73HA) LAMB 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6149-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    LEMON 
    lemon injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6170
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LEMON (UNII: 24RS0A988O) (LEMON - UNII:24RS0A988O) LEMON 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6170-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    LETTUCE 
    lettuce injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6171
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LETTUCE (UNII: 5PO6NN3RRJ) (LETTUCE - UNII:5PO6NN3RRJ) LETTUCE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6171-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    LIMA BEAN 
    lima bean injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6173
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIMA BEAN (UNII: 112YH1ZMX2) (LIMA BEAN - UNII:112YH1ZMX2) LIMA BEAN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6173-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    LOBSTER 
    lobster injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6174
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LOBSTER, UNSPECIFIED (UNII: ZQ6LG2C39M) (LOBSTER, UNSPECIFIED - UNII:ZQ6LG2C39M) LOBSTER, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6174-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    GOAT MILK 
    goat milk injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6177
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GOAT MILK (UNII: XE5K5I4RP7) (GOAT MILK - UNII:XE5K5I4RP7) GOAT MILK 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6177-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COW MILK 
    milk whole cows injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6178
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COW MILK (UNII: 917J3173FT) (COW MILK - UNII:917J3173FT) COW MILK 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6178-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUSHROOM 
    mushroom agaricus spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6180
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CULTIVATED MUSHROOM (UNII: 54C8E6W6JY) (CULTIVATED MUSHROOM - UNII:54C8E6W6JY) CULTIVATED MUSHROOM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6180-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUSTARD SEED 
    mustard seed injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6181
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUSTARD SEED (UNII: 58RXI817UT) (MUSTARD SEED - UNII:58RXI817UT) MUSTARD SEED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6181-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    OAT 
    oat grain injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6183
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OAT (UNII: Z6J799EAJK) (OAT - UNII:Z6J799EAJK) OAT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6183-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLACK OLIVE 
    olive injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6185
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACK OLIVE (UNII: 2M6QWV94OC) (BLACK OLIVE - UNII:2M6QWV94OC) BLACK OLIVE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6185-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ONION 
    onion injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6186
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6186-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ORANGE 
    orange injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6187
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ORANGE (UNII: 5EVU04N5QU) (ORANGE - UNII:5EVU04N5QU) ORANGE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6187-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    OYSTER 
    oyster injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6189
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OYSTER, UNSPECIFIED (UNII: S614XWR17V) (OYSTER, UNSPECIFIED - UNII:S614XWR17V) OYSTER, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6189-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PEA 
    green pea english injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6191
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEA (UNII: W4X7H8GYFM) (PEA - UNII:W4X7H8GYFM) PEA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6191-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PEACH 
    peach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6192
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEACH (UNII: 3OKE88I3QG) (PEACH - UNII:3OKE88I3QG) PEACH 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6192-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PEANUT 
    peanut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6193
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEANUT (UNII: QE1QX6B99R) (PEANUT - UNII:QE1QX6B99R) PEANUT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6193-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PEAR 
    pear injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6195
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEAR (UNII: 2ZN8DWC0YF) (PEAR - UNII:2ZN8DWC0YF) PEAR 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6195-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PECAN 
    pecan injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6196
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PECAN (UNII: F14P91GB5F) (PECAN - UNII:F14P91GB5F) PECAN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6196-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    GREEN BELL PEPPER 
    bell injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6197
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GREEN BELL PEPPER (UNII: 4J4DOU3HEK) (GREEN BELL PEPPER - UNII:4J4DOU3HEK) GREEN BELL PEPPER 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6197-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLACK PEPPER 
    black pepper injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6198
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF) BLACK PEPPER 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6198-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PINEAPPLE 
    pineapple injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6200
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINEAPPLE (UNII: 2A88ZO081O) (PINEAPPLE - UNII:2A88ZO081O) PINEAPPLE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6200-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PISTACHIO 
    pistachio nut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6202
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PISTACHIO (UNII: 6815CPT6ZJ) (PISTACHIO - UNII:6815CPT6ZJ) PISTACHIO 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6202-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PLUM 
    plum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6203
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PLUM (UNII: 67M3EQ6BE1) (PLUM - UNII:67M3EQ6BE1) PLUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6203-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PORK 
    pork injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6204
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PORK (UNII: O138UB266J) (PORK - UNII:O138UB266J) PORK 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6204-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    POTATO 
    sweet potato injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6205
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD) POTATO 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6205-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    POTATO 
    white potato injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6206
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD) POTATO 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6206-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RICE 
    brown rice injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6208
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BROWN RICE (UNII: 659G217HPG) (BROWN RICE - UNII:659G217HPG) BROWN RICE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6208-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RYE 
    rye injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6210
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RYE (UNII: 0R4AQI398X) (RYE - UNII:0R4AQI398X) RYE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6210-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SALMON 
    salmon injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6212
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALMON, UNSPECIFIED (UNII: 6122W2M0GB) (SALMON, UNSPECIFIED - UNII:6122W2M0GB) SALMON, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6212-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SESAME SEED 
    sesame seed injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6213
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SESAME SEED (UNII: 7Y1255HVXR) (SESAME SEED - UNII:7Y1255HVXR) SESAME SEED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6213-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SHRIMP 
    shrimp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6214
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SHRIMP, UNSPECIFIED (UNII: 1891LE191T) (SHRIMP, UNSPECIFIED - UNII:1891LE191T) SHRIMP, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6214-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SOYBEAN 
    soybean injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6216
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SOYBEAN (UNII: L7HT8F1ZOD) (SOYBEAN - UNII:L7HT8F1ZOD) SOYBEAN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6216-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SPINACH 
    spinach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6218
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SPINACH (UNII: 6WO75C6WVB) (SPINACH - UNII:6WO75C6WVB) SPINACH 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6218-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SQUASH 
    squash injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6219
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SQUASH (UNII: 9961HBA483) (SQUASH - UNII:9961HBA483) SQUASH 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6219-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STRAWBERRY 
    strawberry injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6220
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STRAWBERRY (UNII: 4J2TY8Y81V) (STRAWBERRY - UNII:4J2TY8Y81V) STRAWBERRY 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6220-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CORN 
    sweet corn injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6221
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O) CORN 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6221-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TOMATO 
    tomato injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6224
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TOMATO (UNII: Z4KHF2C175) (TOMATO - UNII:Z4KHF2C175) TOMATO 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6224-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TUNA 
    tuna injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6226
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TUNA, UNSPECIFIED (UNII: V2T3IHT3E2) (TUNA, UNSPECIFIED - UNII:V2T3IHT3E2) TUNA, UNSPECIFIED 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6226-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TURKEY 
    turkey meat injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6229
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TURKEY (UNII: 8E9NT44R8I) (TURKEY - UNII:8E9NT44R8I) TURKEY 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6229-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    VANILLA 
    vanilla injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6230
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    VANILLA (UNII: Q74T35078H) (VANILLA - UNII:Q74T35078H) VANILLA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6230-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ENGLISH WALNUT 
    english walnut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6231
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ENGLISH WALNUT (UNII: 1V3SHR7QB7) (ENGLISH WALNUT - UNII:1V3SHR7QB7) ENGLISH WALNUT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6231-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    WATERMELON 
    watermelon injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6233
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WATERMELON (UNII: 231473QB6R) (WATERMELON - UNII:231473QB6R) WATERMELON 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6233-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    WHEAT 
    whole wheat wheat grain injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6234
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WHEAT (UNII: 4J2I0SN84Y) (WHEAT - UNII:4J2I0SN84Y) WHEAT 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6234-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOS TAURUS SKIN 
    cattle epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6300
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOS TAURUS SKIN (UNII: 7J12CD6O9L) (BOS TAURUS SKIN - UNII:7J12CD6O9L) BOS TAURUS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6300-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COTTON FIBER 
    cattle epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6302
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COTTON FIBER (UNII: 70LDW53ROO) (COTTON FIBER - UNII:70LDW53ROO) COTTON FIBER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6302-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COTTON SEED 
    cottonseed injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6304
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COTTON SEED (UNII: DI0ZRJ0MXN) (COTTON SEED - UNII:DI0ZRJ0MXN) COTTON SEED 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6304-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANIS LUPUS FAMILIARIS SKIN 
    dog epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6306
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (CANIS LUPUS FAMILIARIS SKIN - UNII:X2W7CLE97T) CANIS LUPUS FAMILIARIS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6306-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CAVIA PORCELLUS SKIN 
    guinea pig epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6309
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (CAVIA PORCELLUS SKIN - UNII:GM3H4U6QS8) CAVIA PORCELLUS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6309-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EQUUS CABALLUS SKIN 
    horse epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6311
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (EQUUS CABALLUS SKIN - UNII:88VZV9HGT4) EQUUS CABALLUS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6311-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CEIBA PENTANDRA FIBER 
    kapok injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6312
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (CEIBA PENTANDRA FIBER - UNII:758Z9H9WV9) CEIBA PENTANDRA FIBER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6312-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUS MUSCULUS SKIN 
    mouse epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6314
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUS MUSCULUS SKIN (UNII: 390AN9GB09) (MUS MUSCULUS SKIN - UNII:390AN9GB09) MUS MUSCULUS SKIN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6314-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ORRIS 
    iris x germanica root injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6317
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IRIS X GERMANICA ROOT (UNII: 8N6VTJ9IWV) (IRIS X GERMANICA ROOT - UNII:8N6VTJ9IWV) IRIS X GERMANICA ROOT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6317-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PYRETHRUM CINERARIIFOLIUM 
    pyrethrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6318
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TANACETUM CINERARIIFOLIUM FLOWER (UNII: CGF76TP7X6) (TANACETUM CINERARIIFOLIUM FLOWER - UNII:CGF76TP7X6) TANACETUM CINERARIIFOLIUM FLOWER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6318-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RABBIT 
    rabbit epithelium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6320
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RABBIT (UNII: O5V0F26RUW) (RABBIT - UNII:O5V0F26RUW) RABBIT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6320-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SOLENOPSIS INVICTA 
    fire ant injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6400
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (SOLENOPSIS INVICTA - UNII:5O7CR4P444) SOLENOPSIS INVICTA 0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6400-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PERIPLANETA AMERICANA 
    american cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6403
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (PERIPLANETA AMERICANA - UNII:2RQ1L9N089) PERIPLANETA AMERICANA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6403-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BLATELLA GERMANICA 
    german cockroach injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6405
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLATELLA GERMANICA (UNII: G9O67I0A8Q) (BLATELLA GERMANICA - UNII:G9O67I0A8Q) BLATELLA GERMANICA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6405-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACREMONIUM STRICTUM 
    acremonium strictum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6500
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACREMONIUM STRICTUM (UNII: 3F36V0451W) (ACREMONIUM STRICTUM - UNII:3F36V0451W) ACREMONIUM STRICTUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6500-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALTERNARIA TENUIS 
    alternaria tenuis a alternata injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6502
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6502-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS FUMIGATUS 
    aspergillus fumigatus injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6504
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (ASPERGILLUS FUMIGATUS - UNII:X88DF51T48) ASPERGILLUS FUMIGATUS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6504-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ASPERGILLUS NIGER VAR NIGER 
    aspergillus niger injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6507
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6507-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AUREOBASIDIUM PULLULANS VAR PULLULANS 
    pullularia pullulans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6509
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (AUREOBASIDIUM PULLULANS VAR. PULLUTANS - UNII:D1A2NG69CK) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6509-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BOTRYTIS CINEREA 
    botrytis cinerea injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6512
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BOTRYTIS CINEREA (UNII: TBW53313S7) (BOTRYTIS CINEREA - UNII:TBW53313S7) BOTRYTIS CINEREA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6512-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CANDIDA ALBICANS 
    candida albicans injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6514
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC) CANDIDA ALBICANS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6514-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHAETOMIUM GLOBOSUM 
    chaetomium globosum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6516
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (CHAETOMIUM GLOBOSUM - UNII:5016WB8B8A) CHAETOMIUM GLOBOSUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6516-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM CLADOSPORIOIDES 
    cladosporium cladosporioides hormodendrum clad injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6518
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM CLADOSPORIOIDES (UNII: 4ZWY20GTGO) (CLADOSPORIUM CLADOSPORIOIDES - UNII:4ZWY20GTGO) CLADOSPORIUM CLADOSPORIOIDES 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6518-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CLADOSPORIUM SPHAEROSPERMUM 
    cladosporium sphaerospermum hormodendrum hordei injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6520
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (CLADOSPORIUM SPHAEROSPERMUM - UNII:P87YCA1U8R) CLADOSPORIUM SPHAEROSPERMUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6520-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    COCHLIOBOLUS SATIVUS 
    helminthosporium sorokinianum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6524
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (COCHLIOBOLUS SATIVUS - UNII:3LN5B70U4W) COCHLIOBOLUS SATIVUS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6524-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    EPICOCCUM NIGRUM 
    epicoccum nigrum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6526
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EPICOCCUM NIGRUM (UNII: 87U156LEN7) (EPICOCCUM NIGRUM - UNII:87U156LEN7) EPICOCCUM NIGRUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6526-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FUSARIUM OXYSPORUM VASINFECTUM 
    fusarium spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6529
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FUSARIUM OXYSPORUM VASINFECTUM (UNII: 6M98DC08TZ) (FUSARIUM OXYSPORUM VASINFECTUM - UNII:6M98DC08TZ) FUSARIUM OXYSPORUM VASINFECTUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6529-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    HELMINTHOSPORIUM SOLANI 
    helminthosporium solani spondylocladium injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6533
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (HELMINTHOSPORIUM SOLANI - UNII:U6Z259H815) HELMINTHOSPORIUM SOLANI 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6533-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MUCOR PLUMBEUS 
    mucor spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6536
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUCOR PLUMBEUS (UNII: D7401PWY6E) (MUCOR PLUMBEUS - UNII:D7401PWY6E) MUCOR PLUMBEUS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6536-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    NEUROSPORA INTERMEDIA 
    neurospora spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6538
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (NEUROSPORA INTERMEDIA - UNII:2072U60DUI) NEUROSPORA INTERMEDIA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6538-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    KHUSKIA ORYZAE 
    nigrospora spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6540
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KHUSKIA ORYZAE (UNII: VK8C112WTS) (KHUSKIA ORYZAE - UNII:VK8C112WTS) KHUSKIA ORYZAE 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6540-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PHOMA EXIGUA VAR EXIGUA 
    phoma herbarum injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6543
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHOMA EXIGUA VAR. EXIGUA (UNII: 8JAG41IE4M) (PHOMA EXIGUA VAR. EXIGUA - UNII:8JAG41IE4M) PHOMA EXIGUA VAR. EXIGUA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6543-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHIZOPUS ARRHIZUS VAR ARRHIZUS 
    rhizopus spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6545
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHIZOPUS ARRHIZUS VAR. ARRHIZUS (UNII: 8476849N1Y) (RHIZOPUS ARRHIZUS VAR. ARRHIZUS - UNII:8476849N1Y) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6545-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RHODOTORULA RUBRA 
    rhodotorula rubra injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6548
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHODOTORULA RUBRA (UNII: 15W81V867R) (RHODOTORULA RUBRA - UNII:15W81V867R) RHODOTORULA RUBRA 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6548-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    USTILAGO MAYDIS 
    corn smut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6550
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6550-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    USTILAGO TRITICI 
    wheat smut injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6552
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    USTILAGO TRITICI (UNII: BV82OL2IZ8) (USTILAGO TRITICI - UNII:BV82OL2IZ8) USTILAGO TRITICI 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6552-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    STEMPHYLIUM SOLANI 
    stemphylium spp injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6553
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STEMPHYLIUM SOLANI (UNII: 1IEK4UDP5M) (STEMPHYLIUM SOLANI - UNII:1IEK4UDP5M) STEMPHYLIUM SOLANI 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6553-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TRICHOPHYTON MENTAGROPHYTES 
    trichophyton mentagrophytes injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6556
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (TRICHOPHYTON MENTAGROPHYTES - UNII:199I7J3JIV) TRICHOPHYTON MENTAGROPHYTES 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6556-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM 
    yeast saccharomyces cerevisiae injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6558
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - UNII:3Y1PE1GCIG) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.10 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6558-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACACIA 
    acacia injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6600
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACACIA (UNII: 5C5403N26O) (ACACIA - UNII:5C5403N26O) ACACIA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6600-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ALNUS INCANA SSP RUGOSA POLLEN 
    white alder injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6601
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (ALNUS INCANA SUBSP. RUGOSA POLLEN - UNII:605T96G8Y5) ALNUS INCANA SUBSP. RUGOSA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6601-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MEDICAGO SATIVA POLLEN 
    alfalfa injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6602
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MEDICAGO SATIVA POLLEN (UNII: G515RAI9FY) (MEDICAGO SATIVA POLLEN - UNII:G515RAI9FY) MEDICAGO SATIVA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6602-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FRAXINUS AMERICANA POLLEN 
    white ash injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6603
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6603-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PASPALUM NOTATUM POLLEN 
    bahia grass injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6605
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (PASPALUM NOTATUM POLLEN - UNII:V003SHB7VK) PASPALUM NOTATUM POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6605-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MORELLA CERIFERA POLLEN 
    bayberry wax myrtle injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6606
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6606-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    FAGUS GRANDIFOLIA POLLEN 
    beech injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6607
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6607-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BETULA LENTA POLLEN 
    black birch injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6608
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6608-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BETULA NIGRA POLLEN 
    river birch red injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6609
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6609-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    BETULA LENTA POLLEN 
    white birch injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6610
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6610-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACER NEGUNDO POLLEN 
    box elder ash leaf maple injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6612
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6612-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AMARANTHUS PALMERI POLLEN 
    carelessweed injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6613
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (AMARANTHUS PALMERI POLLEN - UNII:1GH3WV23KH) AMARANTHUS PALMERI POLLEN 0.025 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6613-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    JUNIPERUS ASHEI POLLEN 
    mountain cedar injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6614
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6614-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    JUNIPERUS VIRGINIANA POLLEN 
    red cedar injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6615
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6615-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    XANTHIUM STRUMARIUM VAR CANADENSE POLLEN 
    cocklebur injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6616
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (UNII: 0ZK6G3W3BI) (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - UNII:0ZK6G3W3BI) XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6616-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    POPULUS DELTOIDES POLLEN 
    eastern cottonwood common injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6618
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6618-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CUPRESSUS ARIZONICA POLLEN 
    arizona cypress injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6619
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF) CUPRESSUS ARIZONICA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6619-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    TAXODIUM DISTICHUM POLLEN 
    bald cypress injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6620
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TAXODIUM DISTICHUM POLLEN (UNII: O12H03B41R) (TAXODIUM DISTICHUM POLLEN - UNII:O12H03B41R) TAXODIUM DISTICHUM POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6620-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RUMEX ACETOSELLA POLLEN 
    sour dock sheep sorrel injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6621
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (RUMEX ACETOSELLA POLLEN - UNII:N52MIQ81ZW) RUMEX ACETOSELLA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6621-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    RUMEX CRISPUS POLLEN 
    yellow dock injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6622
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (RUMEX CRISPUS POLLEN - UNII:V825XJG64G) RUMEX CRISPUS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6622-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ULMUS AMERICANA POLLEN 
    american elm injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6623
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6623-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SOLIDAGO CANADENSIS POLLEN 
    goldenrod injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6625
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (SOLIDAGO CANADENSIS POLLEN - UNII:644CZ16IR5) SOLIDAGO CANADENSIS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6625-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CELTIS OCCIDENTALIS POLLEN 
    hackberry injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6626
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (CELTIS OCCIDENTALIS POLLEN - UNII:68R9X9Y96X) CELTIS OCCIDENTALIS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6626-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CARYA OVATA POLLEN 
    shagbark hickory injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6627
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6627-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SORGHUM HALEPENSE POLLEN 
    johnson grass injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6629
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (SORGHUM HALEPENSE POLLEN - UNII:577VA5B4HP) SORGHUM HALEPENSE POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6629-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    JUNIPERUS CALIFORNICA POLLEN 
    western juniper injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6630
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS CALIFORNICA POLLEN (UNII: 0H1V4V5V9L) (JUNIPERUS CALIFORNICA POLLEN - UNII:0H1V4V5V9L) JUNIPERUS CALIFORNICA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6630-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    KOCHIA SCOPARIA POLLEN 
    kochia firebush injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6631
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (BASSIA SCOPARIA POLLEN - UNII:07A108ZKW5) BASSIA SCOPARIA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6631-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CHENOPODIUM ALBUM POLLEN 
    lambs quarters injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6632
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (CHENOPODIUM ALBUM POLLEN - UNII:098LKX5NCN) CHENOPODIUM ALBUM POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6632-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACER RUBRUM POLLEN 
    red maple injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6634
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6634-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ACER SACCHARUM POLLEN 
    sugar maple injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6635
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6635-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    IVA XANTHIFOLIA POLLEN 
    burweed marshelder injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6636
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CYCLACHAENA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J) (CYCLACHAENA XANTHIFOLIA POLLEN - UNII:V80TPZ0T6J) CYCLACHAENA XANTHIFOLIA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6636-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    IVA ANNUA VAR ANNUA POLLEN 
    rough marshelder injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6637
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IVA ANNUA POLLEN (UNII: Y2U5S5PF22) (IVA ANNUA POLLEN - UNII:Y2U5S5PF22) IVA ANNUA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6637-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PROSOPIS JULIFLORA POLLEN 
    mesquite injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6638
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6638-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ARTEMISIA VULGARIS POLLEN 
    common mugwort injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6639
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (ARTEMISIA VULGARIS POLLEN - UNII:ANT994T71D) ARTEMISIA VULGARIS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6639-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MORUS RUBRA POLLEN 
    red mulberry injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6640
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6640-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    MORUS ALBA POLLEN 
    white mulberry injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6641
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6641-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    QUERCUS RUBRA POLLEN 
    red oak injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6642
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6642-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    QUERCUS VIRGINIANA POLLEN 
    virginia live oak injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6643
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6643-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    QUERCUS ALBA POLLEN 
    white oak injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6644
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6644-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    OLEA EUROPAEA POLLEN 
    olive pollen injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6646
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6646-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SYAGRUS ROMANZOFFIANA POLLEN 
    queen palm coco palm injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6647
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB) SYAGRUS ROMANZOFFIANA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6647-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    CARYA ILLINOINENSIS POLLEN 
    pecan pollen injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6648
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6648-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AMARANTHUS RETROFLEXUS POLLEN 
    rough pigweed injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6649
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (AMARANTHUS RETROFLEXUS POLLEN - UNII:73B14PX5FW) AMARANTHUS RETROFLEXUS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6649-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PINUS STROBUS POLLEN 
    white pine injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6651
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS STROBUS POLLEN (UNII: TX1ER5UV3T) (PINUS STROBUS POLLEN - UNII:TX1ER5UV3T) PINUS STROBUS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6651-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    PLANTAGO LANCEOLATA POLLEN 
    english plantain injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6652
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (PLANTAGO LANCEOLATA POLLEN - UNII:DO87T1U2CI) PLANTAGO LANCEOLATA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6652-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    POPULUS ALBA POLLEN 
    white poplar injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6654
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P) POPULUS ALBA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6654-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    LIGUSTRUM VULGARE POLLEN 
    privet injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6656
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E) LIGUSTRUM VULGARE POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6656-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ELYMUS REPENS POLLEN 
    quack grass injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6657
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (ELYMUS REPENS POLLEN - UNII:ON2T85TA2O) ELYMUS REPENS POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6657-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    AMBROSIA TRIFIDA POLLEN 
    tall ragweed giant injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6658
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (AMBROSIA TRIFIDA POLLEN - UNII:KU1V1898XX) AMBROSIA TRIFIDA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6658-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    SALSOLA KALI POLLEN 
    russian thistle injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6659
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (SALSOLA KALI POLLEN - UNII:2MH135KC6G) SALSOLA KALI POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6659-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965
    ARTEMISIA TRIDENTATA POLLEN 
    common sagebrush injection, solution
    Product Information
    Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6670
    Route of Administration PERCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (ARTEMISIA TRIDENTATA POLLEN - UNII:YI19RB8YFD) ARTEMISIA TRIDENTATA POLLEN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 1 mL
    PHENOL (UNII: 339NCG44TV) 0.004 mL  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.009 g  in 1 mL
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) 0.00275 g  in 1 mL
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0268-6670-06 5 mL in 1 VIAL, MULTI-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA103753 01/01/1965