Available Formats

• 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.

                   

   

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• SPL UNCLASSIFIED SECTION

  ALLERGENIC EXTRACTS, FOR DIAGNOSTIC USE ONLY

  DIRECTIONS FOR USE

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• 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.

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• 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).

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• 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.

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• 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.

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• 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.

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• 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.

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• 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.

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• 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.

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• 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.

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• 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.

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• 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.

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• 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

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• PRINCIPAL DISPLAY PANEL

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

  

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• INGREDIENTS AND APPEARANCE

  HOUSE DUST  house dust injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6000 Route of Administration PERCUTANEOUS

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOUSE DUST (UNII: EYO007VX98) (HOUSE DUST - UNII:EYO007VX98) HOUSE DUST 10000 [PNU]  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:0268-6000-06 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 06/30/2013

  ALMOND  almond food injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6100 Route of Administration PERCUTANEOUS

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALMOND (UNII: 3Z252A2K9G) (ALMOND - UNII:3Z252A2K9G) ALMOND 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:0268-6100-06 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

  APPLE  apple food injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6101 Route of Administration PERCUTANEOUS

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APPLE (UNII: B423VGH5S9) (APPLE - UNII:B423VGH5S9) APPLE 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:0268-6101-06 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

  APRICOT  apricot injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6102 Route of Administration PERCUTANEOUS

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APRICOT (UNII: 269CJD5GZ9) (APRICOT - UNII:269CJD5GZ9) APRICOT 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:0268-6102-06 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

  ASPARAGUS  asparagus injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6103 Route of Administration PERCUTANEOUS

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPARAGUS (UNII: Z1EJP3037Z) (ASPARAGUS - UNII:Z1EJP3037Z) ASPARAGUS 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:0268-6103-06 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 BLA BLA103753 01/01/1965

  AVOCADO  avocado injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6104 Route of Administration PERCUTANEOUS

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOCADO (UNII: SDS87L369F) (AVOCADO - UNII:SDS87L369F) AVOCADO 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:0268-6104-06 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 BLA BLA103753 01/01/1965

  BANANA  banana injection, solution

  Product Information Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:0268-6105 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