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California Black Oak (Nelco Laboratories, Inc.)

Available Formats

Dosage Form Package Information Links
INJECTION, SOLUTION 5 mL in 1 VIAL, MULTI-DOSE (36987-2837-1) Label Information
INJECTION, SOLUTION 10 mL in 1 VIAL, MULTI-DOSE (36987-2837-2) Label Information
INJECTION, SOLUTION 30 mL in 1 VIAL, MULTI-DOSE (36987-2837-3) Label Information
INJECTION, SOLUTION 50 mL in 1 VIAL, MULTI-DOSE (36987-2837-4) Label Information

Complete California Black Oak Information

  • BOXED WARNING(What is this?)

    WARNING

    Diagnostic and therapeutic allergenic extracts are intended to be administered by a physician who is an allergy specialist and experienced in allergenic diagnostic testing and immunotherapy and the emergency care of anaphylaxis.

    This product should not be injected intravenously. Deep subcutaneous routes have been safe. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and/or death. (See Adverse Reactions)

    Serious adverse reactions should be reported to Nelco Laboratories immediately and a report filed to: MedWatch, The FDA Medical Product Problem Reporting Program, at 5600 Fishers Lane, Rockville, Md. 20852-9787, call 1-800-FDA-1088.

    Extreme caution should be taken when using allergenic extracts for patients who are taking beta-blocker medications. In the event of a serious adverse reaction associated with the use of allergenic extracts, patients receiving beta-blockers may not be responsive to epinephrine or inhaled brochodialators.(1)(See Precautions)

    Allergenic extracts should be used with caution for patients with unstable or steroid-dependent asthma or underlying cardiovascular disease. (See Contraindications)


  • DESCRIPTION

    Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts)

    For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections.


  • CLINICAL PHARMACOLOGY

    The pharmacological action of allergenic extracts used diagnostically is based on the liberation of histamine and other substances when the allergen reacts with IgE antibodies attached to the mast cells. When allergenic extracts are used for immunotherapy, the effect is an increase in immunoglobulin G (IgG) and an increased T suppresser lymphocyte which interferes with the allergic response.(2) With repeated administration of allergenic extracts changes develop in regards to IgG and IgE production and mediator-releasing cells. The histamine release response is reduced in some patients.


  • INDICATIONS AND USAGE

    Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity.

    Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.


  • CONTRAINDICATIONS

    Allergenic extracts should not be used if the patient has asthma, cardiovascular disease, emphysema, diabetes, bleeding diathesis or pregnancy, unless a specific diagnosis of type 1 allergic disease is made based on skin testing and the benefits of treatment outweigh the risks of an adverse reaction during testing or treatment. Allergenic extracts are not indicated for use in patients who are not clinically allergic or who are not skin reactive to an allergen. Allergenic extracts should be discontinued or the concentration of potency substantially reduced in patients who experience unacceptable adverse reactions.


  • WARNINGS

    DO NOT INJECT INTRAVENOUSLY.

    Epinephrine 1:1000 should be available.

    Concentrated extracts must be diluted with sterile diluent prior to first use on a patient for treatment or intradermal testing. All concentrates of glycerinated allergenic extracts have the ability to cause serious local and systemic reactions including death in sensitive patients. Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and /or death.(4)(See Adverse Reactions) An allergenic extract should be temporarily withheld from patients or the dose of the extract adjusted downward if any of the following conditions exist: (1) Severe symptoms of rhinitis and/or asthma (2) Infections or flu accompanied by fever and (3) Exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection. When switching patients to a new lot of the same extract the initial dose should be reduced 3/4 so that 25% of previous dose is administered.


  • PRECAUTIONS

    GENERAL: Epinephrine 1:1000 should be available as well as personnel trained in administering emergency treatment. Allergenic Extracts are not intended for intravenous injections. For safe and effective use of allergenic extracts, sterile diluents, sterile vials, sterile syringes should be used and aseptic precautions observed when making a dilution and/or administering the allergenic extract injection. A sterile tuberculin syringe graduated in 0.1 ml units to measure each dose for the prescribed dilution should be used. To reduce the risk of an occurrence of adverse reactions, begin with a careful personal history plus a physical exam. Confirm your findings with scratch or intradermal skin testing.

    Standardized extracts are those labeled in AU/ml units or BAU/ml units. Standardized extracts are not interchangeable with extracts previously labeled as wt/vol or PNU/ml. Before administering a standardized extract, read the accompanying insert contained with standardized extracts.

    Information for Patients: All concentrates of allergenic extracts have the ability to cause serious local and systemic reactions including death in sensitive patients. Patients should be informed of this risk prior to skin testing and immunotherapy. Patients should be instructed to recognize adverse reaction symptoms that may occur and to report all adverse reactions to a physician. Patients should be instructed to remain in the office for 30 minutes during testing using allergenic extracts and at least 30 minutes after therapeutic injections using allergenic extracts.

    DRUG INTERACTIONS: Some drugs may affect the reactivity of the skin; patients should be instructed to avoid medications, particularly antihistamines and sympathomimetic drugs, for at least 24 hours prior to skin testing. Antihistamines and Hydroxyzine can significantly inhibit the immediate skin test reactions as they tend to neutralize or antagonize the action of histamine.(3) This effect has been primarily documented when testing was performed within 1 to 2 hours after drug ingestion. Partial inhibition of the skin test reaction had been observed for longer periods. Epinephrine injection inhibits the immediate skin test reactions for several hours. Patients on delayed absorption antihistamine tablets should be free of such medication for 48 hours before testing. Patients using Astemizole (Hismanal) may experience prolonged suppression and should be free from such medication for up to 6 to 8 weeks prior to testing. Refer to package insert from an applicable long acting antihistamine manufacturer for additional information.

    Extreme caution should be taken when using allergenic extracts on patients who are taking beta-blockers. Patients on non-selective beta blockers may be more reactive to allergens given for testing or treatment and may be unresponsive to the usual doses of epinephrine used to treat allergic reactions.

    Carcinogenesis, mutagenesis, impairment of fertility:

    Long term studies in animals have not been conducted with allergenic extracts to determine their potential carcinogenicity, mutagenicity or impairment of fertility.

    Pregnancy: Category C: Animal reproduction studies have not been conducted with Allergenic Extracts. It is not known whether allergenic extracts can cause fetal harm when administered to pregnant women or can affect reproduction capacity. Allergenic extracts should be given to pregnant women only if clearly needed.

    Nursing Mothers: It is not known whether this drug appears in human milk. Because many drugs are detected in human milk, caution should be exercised when Allergenic Extracts are administered to a nursing woman. There are no current studies on extract components in human milk, or their effect on the nursing infant.

    Pediatric Use: Allergenic extracts have been used in children over two years of age.(5)


  • ADVERSE REACTIONS

    Adverse systemic reactions usually occur within minutes and consist primarily of allergic symptoms such as: generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, itching of nose and throat, breathlessness, dyspnea, coughing, hypotension and marked perspiration. Less commonly, nausea, emesis, abdominal cramps, diarrhea and uterine contractions may occur. Severe reactions may cause anaphylaxis or shock and loss of consciousness and rarely death.

    The treatment of systemic allergic reactions is dependent upon the system complex. Antihistamines may offer relief of recurrent urticaria, associated skin reactions and gastrointestinal symptoms. Corticosteroids may provide benefit if symptoms are prolonged or recurrent. (See Overdose section)

    Local Reactions consisting of erythema, itching, swelling tenderness and sometimes pain may occur at the injection site. These reactions may appear within a few minutes to hours and persist for several days. Local cold applications and oral antihistamines may be effective treatment. For marked and prolonged local reactions the use of antihistamines or anti-inflammatory medications may be dictated. Serious adverse reactions should be reported to Nelco Laboratories immediately and a report can be filed to: MedWatch, The FDA Medical Product Problem Reporting Program, at 5600 Fishers Lane, Rockville, MD 20852-9787, call 1-800-FDA-1088.


  • OVERDOSAGE

    Overdose can cause both local and systemic reactions. An overdose may be prevented by careful observation and questioning of the patient about the previous injection.

    If systemic or anaphylactic reaction, does occur, apply a tourniquet above the site of injection and inject intramuscularly or subcutaneously 0.3 to 0.5ml of 1:1000 Epinephrine Hydrochloride into the opposite arm. The dose may be repeated in 5-10 minutes if necessary. Loosen the tourniquet at least every 10 minutes. The Epinephrine Hydrochloride 1:1000 dose for infants to 2 years is 0.05 to 0.1 ml, for children 2 to 6 years it is 0.15 ml, for children 6-12 years it is 0.2 ml.

    Patients unresponsive to Epinephrine may be treated with Theophylline. Studies on asthmatic subjects reveal that plasma concentrations of Theophylline of 5 to 20 µg/ml are associated with therapeutic effects. Toxicity is particularly apparent at concentrations greater than 20 µg/ml. A loading dose of Aminophylline of 5.8 mg/kg intravenously followed by 0.9 mg/kg per hour results in plasma concentrations of approximately 10 µg/ml for patients not previously receiving theophylline. (Mitenko and Ogilive, Nicholoson and Chick,1973)

    Other beta-adrenergic drugs such as Isoproterenol, Isoetharine, or Albuterol may be used by inhalation. The usual dose to relieve broncho-constriction in asthma is 0.5 ml of the 0.5% solution for Isoproterenol HCl. The Albuterol inhaler delivers approximately 90 mcg of Albuterol from the mouthpiece. The usual dosage for adults and children would be two inhalations repeated every 4-6 hours. Isoetharine supplied in the Bronkometer unit delivers approximately 340 mcg Isoetharine. The average dose is one to two inhalations. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require oxygen, intubation and the use of life support systems.


  • DOSAGE AND ADMINISTRATION

    General Precautions

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

    The dosage of allergenic extracts is dependent upon the purpose of the administration. Allergenic extracts can be administered for diagnostic use or for therapeutic use.

    When allergenic extracts are administered for diagnostic use, the dosage is dependent upon the method used. Two methods commonly used are scratch testing and intradermal testing. Both types of tests result in a wheal and flare response at the site of the test which usually develops rapidly and may be read in 20-30 minutes.

    Diagnostic Use: Scratch Testing Method

    Scratch testing is considered a simple and safe method although less sensitive than the intradermal test. Scratch testing can be used to determine the degree of sensitivity to a suspected allergen before using the intradermal test. This combination lessens the severity of response to an allergen which can occur in a very sensitive patient.

    The most satisfactory testing site is the patient's back or volar surface of the arms from the axilla to 2.5 or 5cm above the wrist, skipping the anti-cubital space. If using the back as a testing site, the most satisfactory area are from the posterior axillary fold to 2.5 cm from the spinal column, and from the top of the scapula to the lower rib margins.

    Allergenic extracts for diagnostic use are to be administered in the following manner: To scratch surface of skin, use a circular scarifier. Do not draw blood. Tests sites should be 4 cm apart to allow for wheal and flare reaction. 1-30 scratch tests may be done at a time. A separate sterile scratch instrument is to be used on each patient to prevent transmission of homologous serum hepatitis or other infectious agents from one patient to another.

    The recommended usual dosage for Scratch testing is one drop of allergen applied to each scratch site. Do not let dropper touch skin. Always apply a control scratch with each test set. Sterile Diluent (for a negative control) is used in exactly the same way as an active test extract. Histamine may be used as a positive control. Scratch or prick test sites should be examined at 15 and 30 minutes. To prevent excessive absorption, wipe off antigens producing large reactions as soon as the wheal appears. Record the size of the reaction.

    Interpretation of Scratch Test

    Skin tests are graded in terms of the wheal and erythema response noted at 10 to 20 minutes. Wheal and erythema size may be recorded by actual measurement as compared with positive and negative controls. A positive reaction consists of an area of erythema surrounding the scarification that is larger than the control site. For uniformity in reporting reactions, the following system is recommended. (6)

    REACTION SYMBOL CRITERIA
    Negative - No wheal. Erythema absent or very slight (not more than 1 mm diameter).
    One Plus + Wheal absent or very slight erythema present (not more than 3 mm diameter).
    Two Plus ++ Wheal not more than 3mm or erythema not more than 5mm diameter.
    Three Plus +++ Wheal between 3mm and 5mm diameter, with erythema. Possible pseudopodia and itching.
    Four Plus ++++ A larger reaction with itching and pain.

    Diagnostic Use: Intradermal Skin Testing Method

    Do not perform intradermal test with allergens which have evoked a 2+ or greater response to a Scratch test. Clean test area with alcohol, place sites 5 cm apart using separate sterile tuberculin syringe and a 25 gauge needle for each allergen. Insert needle tip, bevel up, into intracutaneous space. Avoid injecting into blood vessel, pull back gently on syringe plunger, if blood enters syringe change position of needle. The recommended dosage and range for intradermal testing is 0.05 ml of not more than 100 pnu/ml or 1:1000 w/v (only if puncture test is negative) of allergenic extract. Inject slowly until a small bleb is raised. It is important to make each bleb the same size.

    Interpretation of Intradermal Test:

    The patient's reaction is graded on the basis of size of wheal and flare as compared to control. Use 0.05 ml sterile diluent as a negative control to give accurate interpretation. The tests may be accurately interpreted only when the saline control site has shown a negative response. Observe patient for at least 30 minutes. Tests can be read in 15-20 minutes. Edema, erythema and presence of pseudopods, pain and itching may be observed in 4 plus reactions. For uniformity in reporting reactions the following system is recommended. (6)

    REACTION SYMBOL CRITERIA
    Negative - No increase in size of bleb since injection. No erythema.
    One Plus + An increase in size of bleb to a wheal not more than 5mm diameter, with associated erythema.
    Two Plus ++ Wheal between 5mm and 8mm diameter with erythema.
    Three Plus +++ Wheal between 8mm and 12mm diameter with erythema and possible pseudopodia and itching or pain.
    Four Plus ++++ Any larger reaction with itch and pain, and possible diffuse blush of the skin surrounding the reaction area.

    Therapeutic Use: Recommended dosage & range

    Check the listed ingredients to verify that it matches the prescription ordered. When using a prescription set, verify the patient's name and the ingredients listed with the prescription order. Assess the patient's physical and emotional status prior to giving as injection. Do not give injections to patients who are in acute distress. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    Dosage of allergenic extracts is a highly individualized matter and varies according to the degree of sensitivity of the patient, his clinical response and tolerance to the extract administered during the early phases of an injection regimen. The dosage must be reduced when transferring a patient from non-standardized or modified extract to standardized extract. Any evidence of a local or generalized reaction requires a reduction in dosage during the initial stages of immunotherapy as well as during maintenance therapy. After therapeutic injections patients should be observed for at least 20 minutes for reaction symptoms.

    SUGGESTED DOSAGE SCHEDULE

    The following schedule may act as a guide. This schedule has not been proven to be safe or effective. Sensitive patients may begin with smaller doses of weaker solutions and the dosage increments can be less.

    STRENGTH DOSE VOLUME
    Vial #1 1 0.05
    1:100,000 w/v 2 0.10
    10 pnu/ml 3 0.15
    1 AU/ml 4 0.20
    1 BAU/ml 5 0.30
    6 0.40
    7 0.50
    Vial #2 8 0.05
    1:10,000 w/v 9 0.10
    100 pnu/ml 10 0.15
    10 AU/ml 11 0.20
    10 BAU/ml 12 0.30
    13 0.40
    14 0.50
    Vial #3 15 0.05
    1:1,000 w/v 16 0.10
    1,000 pnu/ml 17 0.15
    100 AU/ml 18 0.20
    100 BAU/ml 19 0.30
    20 0.40
    21 0.50
    Vial #4 22 0.05
    1:100 w/v 23 0.07
    10,000 pnu/ml 24 0.10
    1,000 AU/ml 25 0.15
    1,000 BAU/ml 26 0.20
    27 0.25
    Maintenance Refill 28 0.25
    1:100 w/v 29 0.25
    10,000 pnu/ml 30 0.25
    1,000 AU/ml 31 0.25
    1,000 BAU/ml 32 0.25
    subsequent doses 33 0.25

    Preparation Instructions:

    All dilutions may be made using sterile buffered diluent. The calculation may be based on the following ratio:

    Volume desired x Concentration desired = Volume needed x Concentration available.

    Example 1: If a 1:10 w/v extract is available and it is desired to use a 1:1,000 w/v extract substitute as follows:

    Vd x Cd = Vn x Ca

    10ml x 0.001 = Vn x 0.1

    0.1 ml = Vn

    Using a sterile technique, remove 0.10 ml of extract from the 1:10 vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting ratio will be a 10 ml vial of 1:1,000 w/v.

    Example 2: If a 10,000 pnu/ml extract is available and it is desired to use a 100 pnu/ml extract substitute as follows:

    10ml x 100 = Vn x 10,000

    0.1 ml = Vn

    Using a sterile technique, remove 0.10 ml of extract from the 10,000 pnu/ml vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting concentration will be a 10 ml vial of 100 pnu/ml.

    Example 3: If a 10,000 AU/ml or BAU/ml extract is available and it is desired to use a 100 AU/ml or BAU/ml extract substitute as follows: Vd x Cd = Vn x Ca

    10ml x 100 = Vn x 10,000

    0.1 ml = Vn

    Using a sterile technique, remove 0.10 ml of extract from the 10,000 AU/ml or BAU/ml vial and place it into a vial containing 9.90 ml of sterile diluent. The resulting concentration will be 10ml vial of 100 AU/ml or BAU/ml.

    Intervals between doses: The optimal interval between doses of allergenic extract has not been definitely established. The amount of allergenic extract is increased at each injection by not more than 50%-100% of the previous amount and the next increment is governed by the response to the last injection. There are three generally accepted methods of pollen hyposensitizing therapy.

    1. PRESEASONAL

    Treatment starts each year 6 to 8 weeks before onset of seasonal symptoms. Maximal dose reached just before symptoms are expected. Injections discontinued during and following season until next year.

    2. CO-SEASONAL

    Patient is first treated during season with symptoms. Low initial doses are employed to prevent worsening of condition. This is followed by an intensive schedule of therapy (i.e. injections given 2 to 3 times per week). Fewer Allergists are resorting to this Co-seasonal therapy because of the availability of more effective, symptomatic medications that allow the patient to go through a season relatively symptom free.

    3. PERENNIAL

    Initially this is the same as pre seasonal. The allergen is administered twice weekly or weekly for about 20 injections to achieve the maximum tolerated dose. Then, maintenance therapy may be administered once a week or less frequently.

    Duration of Treatment: The usual duration of treatment has not been established. A period of two or three years of injection therapy constitutes an average minimum course of treatment.


  • HOW SUPPLIED

    Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml).

    Sizes:

    Diagnostic Scratch: 5 ml dropper application vials

    Diagnostic Intradermal: 5 ml or 10 ml vials.

    Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.


  • STORAGE

    The expiration date of allergen extracts is listed on the container label. Store extracts upon arrival at 2° to 8°C and keep them in this range during office use.

    WARRANTY:We warrant that this product was prepared and tested according to the standards of the FDA and is true to label. Because of biological differences in individuals and because allergenic extracts are manufactured to be potent and because we have no control over the conditions of use, we cannot and do not warrant either a good effect or against an ill effect following use.


  • REFERENCES

    1 Jacobs, Robert L., Geoffrey W.Rake,Jr., et.al. Potentiated Anaphylaxis in Patients with Drug-induced Beta-adrenergic Blockade. J.Allergy & Clin. Immunol., 68(2): 125-127. August 1981.

    2 Ishizaka,K.: Cellular Events in the IgE Antibody Response. Adv. in Immuno. 23:50-75, 1976.

    3. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

    4. Reid,M.J., Lockey,R.F., Turkeltaub,P.C., Platts-Mills,T.A.E., Survey of fatalities from skin testing and immunotherapy 1985-1989. Journal of Allergy Clin. Immunol. 92 (1): 6-15, July 1993.

    5. Murray, A.B., Ferguson, A., Morrison, B., The frequency and severity of cat allergy vs dog allergy in atopic children. J. Allergy Clin. Immunolo: 72, 145-9, 1983.

    6. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.


  • CONTAINER LABELING

    5 mL Stock Intradermal
    5 mL Stock Scratch
    Stock Small Label
    Stock Large Label

  • INGREDIENTS AND APPEARANCE
    ACACIA 
    acacia injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2445
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACACIA BAILEYANA POLLEN (UNII: 59WAV8G5X5) (ACACIA BAILEYANA POLLEN - UNII:59WAV8G5X5) ACACIA BAILEYANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2445-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2445-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2445-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2445-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    RED ALDER 
    red alder injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2453
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (ALNUS RUBRA POLLEN - UNII:Z0F2YK1B7H) ALNUS RUBRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2453-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2453-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2453-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2453-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    TAG ALDER 
    tag alder injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2461
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    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 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2461-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2461-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2461-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2461-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE ALDER 
    white alder injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2469
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALNUS RHOMBIFOLIA POLLEN (UNII: 7X8HL8GRTM) (ALNUS RHOMBIFOLIA POLLEN - UNII:7X8HL8GRTM) ALNUS RHOMBIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2469-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2469-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2469-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2469-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ARIZONA ASH 
    arizona ash injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2477
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (FRAXINUS VELUTINA POLLEN - UNII:LJT6I6Z8FD) FRAXINUS VELUTINA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2477-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2477-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2477-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2477-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    OREGON ASH 
    oregon ash injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2485
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FRAXINUS LATIFOLIA POLLEN (UNII: 1FH355G8HF) (FRAXINUS LATIFOLIA POLLEN - UNII:1FH355G8HF) FRAXINUS LATIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2485-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2485-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2485-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2485-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE ASH 
    white ash injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2493
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (FRAXINUS AMERICANA POLLEN - UNII:G684LX721Q) FRAXINUS AMERICANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2493-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2493-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2493-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2493-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ASPEN 
    aspen injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2501
    Route of Administration SUBCUTANEOUS, INTRADERMAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS TREMULOIDES POLLEN (UNII: 928OC2TJDA) (POPULUS TREMULOIDES POLLEN - UNII:928OC2TJDA) POPULUS TREMULOIDES POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2501-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2501-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2501-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2501-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BAYBERRY 
    bayberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2509
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (MORELLA CERIFERA POLLEN - UNII:LC8MEV9S89) MORELLA CERIFERA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2509-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2509-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2509-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2509-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    AMERICAN BEECH 
    american beech injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2517
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FAGUS GRANDIFOLIA POLLEN (UNII: 34X886W1H4) (FAGUS GRANDIFOLIA POLLEN - UNII:34X886W1H4) FAGUS GRANDIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2517-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2517-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2517-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2517-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BEEFWOOD/AUSTRALIAN PINE 
    beefwood/australian pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2525
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CASUARINA EQUISETIFOLIA POLLEN (UNII: OZJ4OE173N) (CASUARINA EQUISETIFOLIA POLLEN - UNII:OZJ4OE173N) CASUARINA EQUISETIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2525-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2525-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2525-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2525-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BIRCH 
    birch injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2533
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BETULA NIGRA POLLEN (UNII: 93963RFO1P) (BETULA NIGRA POLLEN - UNII:93963RFO1P) BETULA NIGRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2533-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2533-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2533-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2533-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BLACK BIRCH 
    black birch injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2541
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BETULA LENTA POLLEN (UNII: JQ5HI5004M) (BETULA LENTA POLLEN - UNII:JQ5HI5004M) BETULA LENTA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2541-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2541-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2541-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2541-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE BIRCH 
    white birch injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2549
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (BETULA POPULIFOLIA POLLEN - UNII:23H70FYJ5U) BETULA POPULIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2549-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2549-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2549-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2549-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BOX ELDER 
    box elder injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2557
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (ACER NEGUNDO POLLEN - UNII:P6K070AR8V) ACER NEGUNDO POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2557-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2557-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2557-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2557-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    MOUNTAIN CEDAR 
    mountain cedar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2565
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2565-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2565-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2565-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2565-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    RED CEDAR 
    red cedar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2573
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (JUNIPERUS VIRGINIANA POLLEN - UNII:PY0JA16R2G) JUNIPERUS VIRGINIANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2573-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2573-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2573-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2573-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SALT CEDAR 
    salt cedar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2581
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TAMARIX GALLICA POLLEN (UNII: 43IR7KR479) (TAMARIX GALLICA POLLEN - UNII:43IR7KR479) TAMARIX GALLICA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2581-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2581-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2581-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2581-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    EASTERN COTTONWOOD 
    eastern cottonwood injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2589
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2589-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2589-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2589-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2589-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    FREMONT COTTONWOOD 
    fremont cottonwood injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2597
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS FREMONTII POLLEN (UNII: 426RHB4302) (POPULUS FREMONTII POLLEN - UNII:426RHB4302) POPULUS FREMONTII POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2597-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2597-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2597-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2597-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WEST COTTONWOOD 
    west cottonwood injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2605
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN - UNII:5928LJ1441) POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2605-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2605-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2605-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2605-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ARIZONA CYPRESS 
    arizona cypress injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2613
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CUPRESSUS ARIZONICA POLLEN (UNII: 232DMH0XVF) (CUPRESSUS ARIZONICA POLLEN - UNII:232DMH0XVF) CUPRESSUS ARIZONICA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2613-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2613-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2613-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2613-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BALD CYPRESS 
    bald cypress injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2621
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TAXODIUM DISTICHUM POLLEN (UNII: O12H03B41R) (TAXODIUM DISTICHUM POLLEN - UNII:O12H03B41R) TAXODIUM DISTICHUM POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2621-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2621-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2621-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2621-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    AMERICAN ELM 
    american elm injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2629
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (ULMUS AMERICANA POLLEN - UNII:89BAT511BD) ULMUS AMERICANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2629-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2629-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2629-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2629-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    CEDAR ELM 
    cedar elm injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2637
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I) (ULMUS CRASSIFOLIA POLLEN - UNII:G82398SD3I) ULMUS CRASSIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2637-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2637-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2637-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2637-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    CHINESE ELM 
    chinese elm injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2645
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ULMUS PUMILA POLLEN (UNII: 030R993R8E) (ULMUS PUMILA POLLEN - UNII:030R993R8E) ULMUS PUMILA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2645-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2645-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2645-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2645-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    EUCALYPTUS 
    eucalyptus injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2653
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (EUCALYPTUS GLOBULUS POLLEN - UNII:7XW7TB10X9) EUCALYPTUS GLOBULUS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2653-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2653-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2653-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2653-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    HAZELNUT 
    hazelnut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2661
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CORYLUS AMERICANA POLLEN (UNII: ZGS382Y3AV) (CORYLUS AMERICANA POLLEN - UNII:ZGS382Y3AV) CORYLUS AMERICANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2661-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2661-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2661-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2661-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SHAGBARK HICKORY 
    shagbark hickory injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2669
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARYA OVATA POLLEN (UNII: 54UN9R2798) (CARYA OVATA POLLEN - UNII:54UN9R2798) CARYA OVATA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2669-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2669-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2669-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2669-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE HICKORY 
    white hickory injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2677
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARYA ALBA POLLEN (UNII: G2A764T54B) (CARYA ALBA POLLEN - UNII:G2A764T54B) CARYA ALBA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2677-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2677-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2677-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2677-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ONE SEED JUNIPER 
    one seed juniper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2685
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS MONOSPERMA POLLEN (UNII: PM6E3FG1QK) (JUNIPERUS MONOSPERMA POLLEN - UNII:PM6E3FG1QK) JUNIPERUS MONOSPERMA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2685-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2685-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2685-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2685-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    PINCHOT JUNIPER 
    pinchot juniper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2693
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS PINCHOTII POLLEN (UNII: S8A4X05W7J) (JUNIPERUS PINCHOTII POLLEN - UNII:S8A4X05W7J) JUNIPERUS PINCHOTII POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2693-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2693-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2693-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2693-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ROCKY MOUNTAIN JUNIPER 
    rocky mountain juniper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2701
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (JUNIPERUS SCOPULORUM POLLEN - UNII:0G82TT8ZFY) JUNIPERUS SCOPULORUM POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2701-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2701-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2701-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2701-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    UTAH JUNIPER 
    utah juniper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2709
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS OSTEOSPERMA POLLEN (UNII: 15L060HV8H) (JUNIPERUS OSTEOSPERMA POLLEN - UNII:15L060HV8H) JUNIPERUS OSTEOSPERMA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2709-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2709-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2709-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2709-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WESTERN JUNIPER 
    western juniper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2717
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUNIPERUS OCCIDENTALIS POLLEN (UNII: 7JWJ3HXZ9U) (JUNIPERUS OCCIDENTALIS POLLEN - UNII:7JWJ3HXZ9U) JUNIPERUS OCCIDENTALIS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2717-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2717-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2717-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2717-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    LINDEN 
    linden injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2725
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TILIA AMERICANA POLLEN (UNII: E2B4Q4BXJG) (TILIA AMERICANA POLLEN - UNII:E2B4Q4BXJG) TILIA AMERICANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2725-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2725-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2725-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2725-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BLACK LOCUST 
    black locust injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2733
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ROBINIA PSEUDOACACIA POLLEN (UNII: 8003NOJ82F) (ROBINIA PSEUDOACACIA POLLEN - UNII:8003NOJ82F) ROBINIA PSEUDOACACIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2733-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2733-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2733-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2733-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    MANGO BLOSSOM 
    mango blossom injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2741
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MANGIFERA INDICA POLLEN (UNII: BS3OW0RZ4K) (MANGIFERA INDICA POLLEN - UNII:BS3OW0RZ4K) MANGIFERA INDICA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2741-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2741-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2741-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2741-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    COAST MAPLE 
    coast maple injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2749
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER MACROPHYLLUM POLLEN (UNII: E4CG5Q55M1) (ACER MACROPHYLLUM POLLEN - UNII:E4CG5Q55M1) ACER MACROPHYLLUM POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2749-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2749-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2749-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2749-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    RED MAPLE 
    red maple injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2757
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER RUBRUM POLLEN (UNII: 700NK45C76) (ACER RUBRUM POLLEN - UNII:700NK45C76) ACER RUBRUM POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2757-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2757-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2757-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2757-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SILVER MAPLE 
    silver maple injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2765
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER SACCHARINUM POLLEN (UNII: 95447163DG) (ACER SACCHARINUM POLLEN - UNII:95447163DG) ACER SACCHARINUM POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2765-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2765-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2765-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2765-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SUGAR MAPLE 
    sugar maple injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2773
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (ACER SACCHARUM POLLEN - UNII:V38QUQ7861) ACER SACCHARUM POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2773-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2773-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2773-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2773-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    MELALEUCA POLLEN 
    melaleuca pollen injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2781
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E) (MELALEUCA QUINQUENERVIA POLLEN - UNII:NX974IRT8E) MELALEUCA QUINQUENERVIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2781-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2781-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2781-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2781-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    MESQUITE 
    mesquite injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2789
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (PROSOPIS JULIFLORA POLLEN - UNII:6EIJ3D04MR) PROSOPIS JULIFLORA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2789-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2789-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2789-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2789-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE MULBERRY 
    white mulberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2797
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MORUS ALBA POLLEN (UNII: 3I9T68187H) (MORUS ALBA POLLEN - UNII:3I9T68187H) MORUS ALBA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2797-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2797-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2797-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2797-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    RED MULBERRY 
    red mulberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2805
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (MORUS RUBRA POLLEN - UNII:9LYI4RTZ52) MORUS RUBRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2805-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2805-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2805-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2805-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    MULBERRY 
    mulberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2813
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML) (BROUSSONETIA PAPYRIFERA POLLEN - UNII:51I6N3XIML) BROUSSONETIA PAPYRIFERA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2813-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2813-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2813-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2813-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BLACK OAK 
    black oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2821
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS VELUTINA POLLEN (UNII: 294L626TT0) (QUERCUS VELUTINA POLLEN - UNII:294L626TT0) QUERCUS VELUTINA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2821-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2821-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2821-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2821-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BURR OAK 
    burr oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2829
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS MACROCARPA POLLEN (UNII: 57BTU4547U) (QUERCUS MACROCARPA POLLEN - UNII:57BTU4547U) QUERCUS MACROCARPA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2829-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2829-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2829-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2829-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    CALIFORNIA BLACK OAK 
    california black oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2837
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS KELLOGGII POLLEN (UNII: 02RVY6X9EC) (QUERCUS KELLOGGII POLLEN - UNII:02RVY6X9EC) QUERCUS KELLOGGII POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2837-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2837-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2837-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2837-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    CALIFORNIA LIVE OAK 
    california live oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2845
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (QUERCUS AGRIFOLIA POLLEN - UNII:VOT5MA71M7) QUERCUS AGRIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2845-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2845-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2845-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2845-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    GAMBIL OAK 
    gambil oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2853
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS GAMBELII POLLEN (UNII: 9HC15X34LX) (QUERCUS GAMBELII POLLEN - UNII:9HC15X34LX) QUERCUS GAMBELII POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2853-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2853-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2853-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2853-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    RED OAK 
    red oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2861
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (QUERCUS RUBRA POLLEN - UNII:SVW19ET93C) QUERCUS RUBRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2861-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2861-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2861-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2861-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    CALIFORNIA VALLEY WHITE OAK 
    california valley white oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2869
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS LOBATA POLLEN (UNII: HGH5K3653K) (QUERCUS LOBATA POLLEN - UNII:HGH5K3653K) QUERCUS LOBATA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2869-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2869-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2869-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2869-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    VIRGINIA LIVE OAK 
    virginia live oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2877
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS VIRGINIANA POLLEN (UNII: 8KDG09A4GO) (QUERCUS VIRGINIANA POLLEN - UNII:8KDG09A4GO) QUERCUS VIRGINIANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2877-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2877-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2877-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2877-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WATER OAK 
    water oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2885
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS NIGRA POLLEN (UNII: 6U600U1326) (QUERCUS NIGRA POLLEN - UNII:6U600U1326) QUERCUS NIGRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2885-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2885-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2885-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2885-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE OAK 
    white oak injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2893
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (QUERCUS ALBA POLLEN - UNII:Z4Y9ZSV4KK) QUERCUS ALBA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2893-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2893-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2893-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2893-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    OLIVE POLLEN 
    olive pollen injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2901
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (OLEA EUROPAEA POLLEN - UNII:43R41XZ627) OLEA EUROPAEA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2901-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2901-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2901-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2901-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ORANGE POLLEN 
    orange pollen injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2909
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CITRUS SINENSIS POLLEN (UNII: 0U790UB32K) (CITRUS SINENSIS POLLEN - UNII:0U790UB32K) CITRUS SINENSIS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2909-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2909-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2909-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2909-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    QUEEN PALM 
    queen palm injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2917
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SYAGRUS ROMANZOFFIANA POLLEN (UNII: 84ZOM591BB) (SYAGRUS ROMANZOFFIANA POLLEN - UNII:84ZOM591BB) SYAGRUS ROMANZOFFIANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2917-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2917-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2917-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2917-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    PECAN POLLEN 
    pecan pollen injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2925
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (CARYA ILLINOINENSIS POLLEN - UNII:PYO4JR720Y) CARYA ILLINOINENSIS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2925-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2925-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2925-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2925-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    PEPPER TREE POLLEN 
    pepper tree pollen injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2933
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SCHINUS MOLLE POLLEN (UNII: M0G28FH9K1) (SCHINUS MOLLE POLLEN - UNII:M0G28FH9K1) SCHINUS MOLLE POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2933-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2933-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2933-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2933-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 12/04/2009
    LOBLOLLY PINE 
    loblolly pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2941
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS TAEDA POLLEN (UNII: 4O1FFR8ARN) (PINUS TAEDA POLLEN - UNII:4O1FFR8ARN) PINUS TAEDA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2941-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2941-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2941-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2941-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    LONGLEAF PINE 
    longleaf pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2949
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS PALUSTRIS POLLEN (UNII: E3A7U1HWIO) (PINUS PALUSTRIS POLLEN - UNII:E3A7U1HWIO) PINUS PALUSTRIS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2949-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2949-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2949-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2949-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    PONDEROSA PINE 
    ponderosa pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2957
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS PONDEROSA POLLEN (UNII: 042SUA2DS9) (PINUS PONDEROSA POLLEN - UNII:042SUA2DS9) PINUS PONDEROSA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2957-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2957-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2957-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2957-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SLASH PINE 
    slash pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2965
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS ELLIOTTII POLLEN (UNII: QJB9OQO689) (PINUS ELLIOTTII POLLEN - UNII:QJB9OQO689) PINUS ELLIOTTII POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2965-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2965-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2965-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2965-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SCRUB PINE 
    scrub pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2973
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS VIRGINIANA POLLEN (UNII: P6818UI2E4) (PINUS VIRGINIANA POLLEN - UNII:P6818UI2E4) PINUS VIRGINIANA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2973-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2973-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2973-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2973-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE PINE 
    white pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2981
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS STROBUS POLLEN (UNII: TX1ER5UV3T) (PINUS STROBUS POLLEN - UNII:TX1ER5UV3T) PINUS STROBUS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2981-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2981-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2981-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2981-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WESTERN WHITE PINE 
    western white pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2989
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS MONTICOLA POLLEN (UNII: 3MDX759C0W) (PINUS MONTICOLA POLLEN - UNII:3MDX759C0W) PINUS MONTICOLA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2989-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2989-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2989-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2989-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    YELLOW PINE 
    yellow pine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2997
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINUS ECHINATA POLLEN (UNII: 96LRW14765) (PINUS ECHINATA POLLEN - UNII:96LRW14765) PINUS ECHINATA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-2997-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-2997-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-2997-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-2997-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    LOMBARDY POPLAR 
    lombardy poplar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3005
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS NIGRA POLLEN (UNII: 0MGE63QPFJ) (POPULUS NIGRA POLLEN - UNII:0MGE63QPFJ) POPULUS NIGRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3005-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3005-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3005-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3005-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WHITE POPLAR 
    white poplar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3013
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (POPULUS ALBA POLLEN - UNII:VU8C8SB23P) POPULUS ALBA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3013-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3013-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3013-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3013-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    PRIVET 
    privet injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3021
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (LIGUSTRUM VULGARE POLLEN - UNII:Y3FRX92Z0E) LIGUSTRUM VULGARE POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3021-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3021-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3021-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3021-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    RUSSIAN OLIVE 
    russian olive injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3029
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ELAEAGNUS ANGUSTIFOLIA POLLEN (UNII: 68P4F4M6VD) (ELAEAGNUS ANGUSTIFOLIA POLLEN - UNII:68P4F4M6VD) ELAEAGNUS ANGUSTIFOLIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3029-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3029-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3029-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3029-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    SWEET GUM 
    sweet gum injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3037
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (LIQUIDAMBAR STYRACIFLUA POLLEN - UNII:5Q246DS5BS) LIQUIDAMBAR STYRACIFLUA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3037-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3037-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3037-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3037-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    EAST SYCAMORE 
    east sycamore injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3045
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (PLATANUS OCCIDENTALIS POLLEN - UNII:E03U1K03LK) PLATANUS OCCIDENTALIS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3045-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3045-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3045-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3045-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    WEST SYCAMORE 
    west sycamore injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3053
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PLATANUS RACEMOSA POLLEN (UNII: BWC8DYU8OS) (PLATANUS RACEMOSA POLLEN - UNII:BWC8DYU8OS) PLATANUS RACEMOSA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3053-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3053-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3053-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3053-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BLACK WALNUT 
    black walnut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3061
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (JUGLANS NIGRA POLLEN - UNII:1BV28146ZR) JUGLANS NIGRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3061-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3061-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3061-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3061-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    CALIFORNIA BLACK WALNUT 
    california black walnut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3069
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUGLANS CALIFORNICA POLLEN (UNII: 2147EPR64I) (JUGLANS CALIFORNICA POLLEN - UNII:2147EPR64I) JUGLANS CALIFORNICA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3069-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3069-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3069-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3069-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ENGLISH WALNUT 
    english walnut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3077
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    JUGLANS REGIA POLLEN (UNII: ARW43087I1) (JUGLANS REGIA POLLEN - UNII:ARW43087I1) JUGLANS REGIA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3077-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3077-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3077-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3077-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BLACK WILLOW 
    black willow injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3085
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (SALIX NIGRA - UNII:QU52J3A5B3) SALIX NIGRA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3085-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3085-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3085-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3085-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    ARROYO WILLOW 
    arroyo willow injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3093
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALIX LASIOLEPIS POLLEN (UNII: 808UWJ59FI) (SALIX LASIOLEPIS POLLEN - UNII:808UWJ59FI) SALIX LASIOLEPIS POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3093-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3093-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3093-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3093-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    PUSSY WILLOW 
    pussy willow injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3101
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALIX DISCOLOR POLLEN (UNII: ER172J09FM) (SALIX DISCOLOR POLLEN - UNII:ER172J09FM) SALIX DISCOLOR POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3101-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3101-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3101-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3101-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    POPLAR 
    poplar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3109
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (POPULUS DELTOIDES POLLEN - UNII:476DVV63WP) POPULUS DELTOIDES POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3109-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3109-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3109-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3109-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    BALSAM POPLAR 
    balsam poplar injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3117
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLEN (UNII: H8QYU50Z2D) (POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLEN - UNII:H8QYU50Z2D) POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLEN 10000 [PNU]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    PHENOL (UNII: 339NCG44TV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-3117-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-3117-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-3117-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-3117-4 50 mL in 1 VIAL, MULTI-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    BLA BLA102192 08/29/1972
    Labeler - Nelco Laboratories, Inc. (054980867)
    Registrant - Nelco Laboratories, Inc. (054980867)
    Establishment
    Name Address ID/FEI Business Operations
    Nelco Laboratories, Inc. 054980867 manufacture