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Yellow Onion (Nelco Laboratories, Inc.)

Available Formats

Dosage Form Package Information Links
INJECTION, SOLUTION 5 mL in 1 VIAL, MULTI-DOSE (36987-1474-1) Label Information
INJECTION, SOLUTION 10 mL in 1 VIAL, MULTI-DOSE (36987-1474-2) Label Information
INJECTION, SOLUTION 50 mL in 1 VIAL, MULTI-DOSE (36987-1474-4) Label Information
INJECTION, SOLUTION 30 mL in 1 VIAL, MULTI-DOSE (36987-1474-3) Label Information

Complete Yellow Onion 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
    RED DELICIOUS APPLE 
    red delicious apple injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1282
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    APPLE (UNII: B423VGH5S9) (APPLE - UNII:B423VGH5S9) APPLE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1282-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1282-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1282-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1282-4 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
    APRICOT 
    apricot injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1286
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    APRICOT (UNII: 269CJD5GZ9) (APRICOT - UNII:269CJD5GZ9) APRICOT 0.05 g  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:36987-1286-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1286-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1286-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1286-4 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
    AVOCADO 
    avocado injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1290
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AVOCADO (UNII: SDS87L369F) (AVOCADO - UNII:SDS87L369F) AVOCADO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1290-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1290-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1290-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1290-4 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
    BANANA 
    banana injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1294
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BANANA (UNII: 4AJZ4765R9) (BANANA - UNII:4AJZ4765R9) BANANA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1294-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1294-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1294-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1294-4 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
    BLACKBERRY 
    blackberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1298
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACKBERRY (UNII: 8A6OMU3I8L) (BLACKBERRY - UNII:8A6OMU3I8L) BLACKBERRY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1298-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1298-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1298-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1298-4 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
    BLUEBERRY 
    blueberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1302
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLUEBERRY (UNII: 253RUG1X1A) (BLUEBERRY - UNII:253RUG1X1A) BLUEBERRY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1302-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1302-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1302-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1302-4 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
    CANTALOUPE 
    cantaloupe injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1306
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CANTALOUPE (UNII: 8QF5D5H6UH) (CANTALOUPE - UNII:8QF5D5H6UH) CANTALOUPE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1306-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1306-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1306-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1306-4 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
    CHERRY BING 
    cherry bing injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1310
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SOUR CHERRY (UNII: 1L29G6428X) (SOUR CHERRY - UNII:1L29G6428X) SOUR CHERRY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1310-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1310-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1310-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1310-4 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
    CRANBERRY 
    cranberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1314
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CRANBERRY (UNII: 0MVO31Q3QS) (CRANBERRY - UNII:0MVO31Q3QS) CRANBERRY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1314-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1314-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1314-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1314-4 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
    DATE 
    date injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1318
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DATE (UNII: H3O7QI5HY7) (DATE - UNII:H3O7QI5HY7) DATE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1318-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1318-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1318-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1318-4 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
    FIG 
    fig injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1322
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FIG (UNII: TGD87RII2U) (FIG - UNII:TGD87RII2U) FIG 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1322-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1322-2 0.1 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1322-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1322-4 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
    GRAPEFRUIT 
    grapefruit injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1330
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GRAPEFRUIT (UNII: O82C39RR8C) (GRAPEFRUIT - UNII:O82C39RR8C) GRAPEFRUIT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1330-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1330-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1330-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1330-4 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
    HONEYDEW MELON 
    honeydew melon injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1334
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HONEYDEW MELON (UNII: RN8P45F92A) (HONEYDEW MELON - UNII:RN8P45F92A) HONEYDEW MELON 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1334-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1334-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1334-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1334-4 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
    LEMON 
    lemon injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1338
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LEMON (UNII: 24RS0A988O) (LEMON - UNII:24RS0A988O) LEMON 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1338-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1338-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1338-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1338-4 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
    LIME 
    lime injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1342
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIME (CITRUS) (UNII: 8CZS546954) (LIME (CITRUS) - UNII:8CZS546954) LIME (CITRUS) 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1342-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1342-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1342-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1342-4 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 
    orange injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1346
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ORANGE (UNII: 5EVU04N5QU) (ORANGE - UNII:5EVU04N5QU) ORANGE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1346-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1346-2 30 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1346-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1346-4 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
    PEACH 
    peach injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1350
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEACH (UNII: 3OKE88I3QG) (PEACH - UNII:3OKE88I3QG) PEACH 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1350-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1350-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1350-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1350-4 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
    PEAR 
    pear injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1354
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEAR (UNII: 2ZN8DWC0YF) (PEAR - UNII:2ZN8DWC0YF) PEAR 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1354-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1354-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1354-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1354-4 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
    PINEAPPLE 
    pineapple injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1358
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PINEAPPLE (UNII: 2A88ZO081O) (PINEAPPLE - UNII:2A88ZO081O) PINEAPPLE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1358-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1358-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1358-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1358-4 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
    PLUM 
    plum injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1362
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PLUM (UNII: 67M3EQ6BE1) (PLUM - UNII:67M3EQ6BE1) PLUM 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1362-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1362-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1362-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1362-4 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
    RASPBERRY 
    raspberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1366
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RASPBERRY (UNII: 4N14V5R27W) (RASPBERRY - UNII:4N14V5R27W) RASPBERRY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1366-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1366-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1366-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1366-4 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
    STRAWBERRY 
    strawberry injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1370
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STRAWBERRY (UNII: 4J2TY8Y81V) (STRAWBERRY - UNII:4J2TY8Y81V) STRAWBERRY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1370-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1370-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1370-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1370-4 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
    TANGERINE 
    tangerine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1374
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TANGERINE (UNII: KH3E3096OO) (TANGERINE - UNII:KH3E3096OO) TANGERINE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1374-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1374-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1374-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1374-4 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
    WATERMELON 
    watermelon injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1378
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WATERMELON (UNII: 231473QB6R) (WATERMELON - UNII:231473QB6R) WATERMELON 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1378-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1378-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1378-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1378-4 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
    ARTICHOKE 
    artichoke injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1382
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARTICHOKE (UNII: 4F3W47PLBE) (ARTICHOKE - UNII:4F3W47PLBE) ARTICHOKE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1382-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1382-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1382-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1382-4 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
    ASPARAGUS 
    asparagus injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1386
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPARAGUS (UNII: Z1EJP3037Z) (ASPARAGUS - UNII:Z1EJP3037Z) ASPARAGUS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1386-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1386-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1386-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1386-4 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 KIDNEY BEANS 
    red kidney beans injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1390
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO) KIDNEY BEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1390-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1390-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1390-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1390-4 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
    LIMA BEANS 
    lima beans injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1394
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIMA BEAN (UNII: 112YH1ZMX2) (LIMA BEAN - UNII:112YH1ZMX2) LIMA BEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1394-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1394-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1394-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1394-4 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
    NAVY BEANS 
    navy beans injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1398
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO) KIDNEY BEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1398-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1398-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1398-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1398-4 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
    STRING BEANS 
    string beans injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1402
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    STRING BEAN (UNII: N9D69B2Q7Y) (STRING BEAN - UNII:N9D69B2Q7Y) STRING BEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1402-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1402-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1402-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1402-4 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
    BEET 
    beet injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1406
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BEET (UNII: N487KM8COK) (BEET - UNII:N487KM8COK) BEET 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1406-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1406-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1406-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1406-4 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
    BROCCOLI 
    broccoli injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1410
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BROCCOLI (UNII: UOI4FT57BZ) (BROCCOLI - UNII:UOI4FT57BZ) BROCCOLI 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1410-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1410-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1410-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1410-4 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
    KIWI 
    kiwi injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1414
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KIWI FRUIT (UNII: 71ES77LGJC) (KIWI FRUIT - UNII:71ES77LGJC) KIWI FRUIT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1414-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1414-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1414-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1414-4 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
    BRUSSELS SPROUT 
    brussels sprout injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1418
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BRUSSELS SPROUT (UNII: KHX46H31F8) (BRUSSELS SPROUT - UNII:KHX46H31F8) BRUSSELS SPROUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1418-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1418-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1418-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1418-4 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
    CABBAGE 
    cabbage injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1422
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CABBAGE (UNII: GW0W1Y9I97) (CABBAGE - UNII:GW0W1Y9I97) CABBAGE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1422-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1422-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1422-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1422-4 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
    CARROT 
    carrot injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1426
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARROT (UNII: L56Z1JK48B) (CARROT - UNII:L56Z1JK48B) CARROT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1426-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1426-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1426-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1426-4 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
    CAULIFLOWER 
    cauliflower injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1430
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CAULIFLOWER (UNII: 138LUT2DWV) (CAULIFLOWER - UNII:138LUT2DWV) CAULIFLOWER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1430-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1430-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1430-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1430-4 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
    CELERY 
    celery injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1434
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CELERY (UNII: 44IDY6DTKX) (CELERY - UNII:44IDY6DTKX) CELERY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1434-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1434-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1434-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1434-4 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 CORN 
    sweet corn injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1438
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O) CORN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1438-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1438-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1438-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1438-4 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
    CUCUMBER 
    cucumber injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1442
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CUCUMBER (UNII: YY7C30VXJT) (CUCUMBER - UNII:YY7C30VXJT) CUCUMBER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1442-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1442-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1442-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1442-4 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
    EGG PLANT 
    egg plant injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1446
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EGGPLANT (UNII: W5K7RAS4VK) (EGGPLANT - UNII:W5K7RAS4VK) EGGPLANT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1446-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1446-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1446-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1446-4 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
    GREEN PEPPER 
    green pepper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1450
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GREEN BELL PEPPER (UNII: 4J4DOU3HEK) (GREEN BELL PEPPER - UNII:4J4DOU3HEK) GREEN BELL PEPPER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1450-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1450-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1450-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1450-4 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
    LENTIL 
    lentil injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1454
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LENTIL (UNII: 6O38V6B52O) (LENTIL - UNII:6O38V6B52O) LENTIL 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1454-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1454-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1454-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1454-4 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
    ICEBERG LETTUCE 
    iceberg lettuce injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1458
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LETTUCE (UNII: 5PO6NN3RRJ) (LETTUCE - UNII:5PO6NN3RRJ) LETTUCE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1458-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1458-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1458-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1458-4 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
    MUSHROOM 
    mushroom injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1462
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CULTIVATED MUSHROOM (UNII: 54C8E6W6JY) (CULTIVATED MUSHROOM - UNII:54C8E6W6JY) CULTIVATED MUSHROOM 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1462-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1462-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1462-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1462-4 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 OLIVE 
    black olive injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1466
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACK OLIVE (UNII: 2M6QWV94OC) (BLACK OLIVE - UNII:2M6QWV94OC) BLACK OLIVE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1466-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1466-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1466-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1466-4 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
    GREEN OLIVE 
    green olive injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1470
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GREEN OLIVE (UNII: 6HD2W46UEG) (GREEN OLIVE - UNII:6HD2W46UEG) GREEN OLIVE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1470-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1470-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1470-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1470-4 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 ONION 
    yellow onion injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1474
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1474-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1474-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1474-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1474-4 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
    PARSLEY 
    parsley injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1478
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PARSLEY (UNII: 58FMD0Q0EV) (PARSLEY - UNII:58FMD0Q0EV) PARSLEY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1478-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1478-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1478-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1478-4 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
    GREEN PEA 
    green pea injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1482
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEA (UNII: W4X7H8GYFM) (PEA - UNII:W4X7H8GYFM) PEA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1482-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1482-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1482-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1482-4 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 POTATO 
    sweet potato injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1486
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SWEET POTATO (UNII: M9WGG9Z9GK) (SWEET POTATO - UNII:M9WGG9Z9GK) SWEET POTATO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1486-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1486-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1486-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1486-4 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 POTATO 
    white potato injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1490
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD) POTATO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1490-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1490-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1490-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1490-4 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
    PUMPKIN 
    pumpkin injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1494
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO (UNII: SYW0QUB89Y) (ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO - UNII:SYW0QUB89Y) ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1494-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1494-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1494-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1494-4 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
    RADISH 
    radish injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1498
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RAPHANUS SATIVUS (UNII: 86R5J6D01D) (RAPHANUS SATIVUS - UNII:86R5J6D01D) RAPHANUS SATIVUS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1498-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1498-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1498-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1498-4 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
    RHUBARB 
    rhubarb injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1502
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RHUBARB (UNII: G280W4MW6E) (RHUBARB - UNII:G280W4MW6E) RHUBARB 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1502-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1502-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1502-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1502-4 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
    SOYBEAN 
    soybean injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1506
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SOYBEAN (UNII: L7HT8F1ZOD) (SOYBEAN - UNII:L7HT8F1ZOD) SOYBEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1506-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1506-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1506-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1506-4 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
    SPINACH 
    spinach injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1510
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SPINACH (UNII: 6WO75C6WVB) (SPINACH - UNII:6WO75C6WVB) SPINACH 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1510-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1510-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1510-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1510-4 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
    SQUASH ZUCCHINI 
    squash zucchini injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1514
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SQUASH (UNII: 9961HBA483) (SQUASH - UNII:9961HBA483) SQUASH 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1514-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1514-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1514-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1514-4 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
    TOMATO 
    tomato injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1518
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TOMATO (UNII: Z4KHF2C175) (TOMATO - UNII:Z4KHF2C175) TOMATO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1518-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1518-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1518-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1518-4 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
    TURNIP 
    turnip injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1522
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TURNIP (UNII: Z38C7FBM49) (TURNIP - UNII:Z38C7FBM49) TURNIP 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1522-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1522-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1522-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1522-4 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
    ALMOND 
    almond injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1526
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALMOND (UNII: 3Z252A2K9G) (ALMOND - UNII:3Z252A2K9G) ALMOND 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1526-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1526-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1526-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1526-4 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
    BRAZIL NUT 
    brazil nut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1530
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BRAZIL NUT (UNII: XKR79OET1K) (BRAZIL NUT - UNII:XKR79OET1K) BRAZIL NUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1530-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1530-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1530-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1530-4 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
    CASHEW 
    cashew injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1534
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CASHEW (UNII: 3H5U5CX7KO) (CASHEW - UNII:3H5U5CX7KO) CASHEW 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1534-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1534-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1534-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1534-4 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
    COCONUT 
    coconut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1538
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    COCONUT (UNII: 3RT3536DHY) (COCONUT - UNII:3RT3536DHY) COCONUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1538-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1538-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1538-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1538-4 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:36987-1542
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ENGLISH WALNUT (UNII: 1V3SHR7QB7) (ENGLISH WALNUT - UNII:1V3SHR7QB7) ENGLISH WALNUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1542-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1542-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1542-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1542-4 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
    FILBERT 
    filbert injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1546
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HAZELNUT (UNII: IW0OM96F6O) (HAZELNUT - UNII:IW0OM96F6O) HAZELNUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1546-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1546-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1546-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1546-4 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
    PEANUT 
    peanut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1550
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEANUT (UNII: QE1QX6B99R) (PEANUT - UNII:QE1QX6B99R) PEANUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1550-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1550-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1550-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1550-4 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 NUT 
    pecan nut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1554
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PECAN (UNII: F14P91GB5F) (PECAN - UNII:F14P91GB5F) PECAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1554-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1554-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1554-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1554-4 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
    PISTACHIO 
    pistachio injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1558
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PISTACHIO (UNII: 6815CPT6ZJ) (PISTACHIO - UNII:6815CPT6ZJ) PISTACHIO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1558-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1558-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1558-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1558-4 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
    BARLEY GRAIN 
    barley grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1562
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BARLEY (UNII: 5PWM7YLI7R) (BARLEY - UNII:5PWM7YLI7R) BARLEY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1562-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1562-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1562-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1562-4 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
    BUCKWHEAT GRAIN 
    buckwheat grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1566
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3) BUCKWHEAT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1566-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1566-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1566-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1566-4 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
    OAT GRAIN 
    oat grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1570
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OAT (UNII: Z6J799EAJK) (OAT - UNII:Z6J799EAJK) OAT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1570-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1570-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1570-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1570-4 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
    RICE GRAIN 
    rice grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1574
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RICE (UNII: 659G217HPG) (RICE - UNII:659G217HPG) RICE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1574-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1574-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1574-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1574-4 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
    RYE GRAIN 
    rye grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1578
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    RYE (UNII: 0R4AQI398X) (RYE - UNII:0R4AQI398X) RYE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1578-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1578-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1578-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1578-4 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
    WHOLE WHEAT GRAIN 
    whole wheat grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1582
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WHEAT (UNII: 4J2I0SN84Y) (WHEAT - UNII:4J2I0SN84Y) WHEAT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1582-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1582-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1582-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1582-4 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
    MACADAMIA NUT 
    macadamia nut injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1586
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MACADAMIA NUT (UNII: Y5432RGW8N) (MACADAMIA NUT - UNII:Y5432RGW8N) MACADAMIA NUT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1586-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1586-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1586-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1586-4 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
    NECTARINE 
    nectarine injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1590
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NECTARINE (UNII: 65KD9TD4C3) (NECTARINE - UNII:65KD9TD4C3) NECTARINE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1590-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1590-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1590-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1590-4 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 
    mango injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1594
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MANGO (UNII: I629I3NR86) (MANGO - UNII:I629I3NR86) MANGO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1594-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1594-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1594-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1594-4 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
    PAPAYA 
    papaya injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1598
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PAPAYA (UNII: KU94FIY6JB) (PAPAYA - UNII:KU94FIY6JB) PAPAYA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1598-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1598-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1598-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1598-4 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
    LEEKS 
    leeks injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1602
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LEEK (UNII: RCU76P419D) (LEEK - UNII:RCU76P419D) LEEK 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1602-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1602-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1602-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1602-4 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
    OKRA 
    okra injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1606
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OKRA (UNII: 51ME2L7STL) (OKRA - UNII:51ME2L7STL) OKRA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1606-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1606-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1606-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1606-4 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
    PARSNIP 
    parsnip injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1610
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PARSNIP (UNII: L2V28YP49S) (PARSNIP - UNII:L2V28YP49S) PARSNIP 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1610-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1610-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1610-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1610-4 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
    CHICK PEA 
    chick pea injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1614
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHICKPEA (UNII: N91637DNW9) (CHICKPEA - UNII:N91637DNW9) CHICKPEA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1614-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1614-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1614-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1614-4 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
    BLACKEYE PEA 
    blackeye pea injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1618
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACK-EYED PEA (UNII: 786YV7B602) (BLACK-EYED PEA - UNII:786YV7B602) BLACK-EYED PEA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1618-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1618-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1618-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1618-4 10 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
    WATERCRESS 
    watercress injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1622
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WATERCRESS (UNII: K5877MW0LE) (WATERCRESS - UNII:K5877MW0LE) WATERCRESS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1622-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1622-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1622-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1622-4 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
    CORN GRAIN 
    corn grain injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1626
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O) CORN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1626-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1626-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1626-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1626-4 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
    CACAO BEAN 
    cacao bean injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1630
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHOCOLATE (UNII: D9108TZ9KG) (CHOCOLATE - UNII:D9108TZ9KG) CHOCOLATE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1630-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1630-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1630-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1630-4 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
    COFFEE 
    coffee injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1634
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72) ARABICA COFFEE BEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1634-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1634-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1634-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1634-4 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
    MALT 
    malt injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1650
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MALT EXTRACT, BARLEY (UNII: R3NBG8914U) (MALT EXTRACT, BARLEY - UNII:R3NBG8914U) MALT EXTRACT, BARLEY 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1650-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1650-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1650-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1650-4 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
    BREWERS YEAST 
    brewers yeast injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1658
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1658-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1658-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1658-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1658-4 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
    ALLSPICE 
    allspice injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1662
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALLSPICE (UNII: I5GZG55B36) (ALLSPICE - UNII:I5GZG55B36) ALLSPICE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1662-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1662-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1662-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1662-4 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
    BAY LEAF 
    bay leaf injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1666
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LAURUS NOBILIS (UNII: 247012Z29Q) (LAURUS NOBILIS - UNII:247012Z29Q) LAURUS NOBILIS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1666-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1666-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1666-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1666-4 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
    CARAWAY SEED 
    caraway seed injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1670
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARAWAY SEED (UNII: W2FH8O2BBE) (CARAWAY SEED - UNII:W2FH8O2BBE) CARAWAY SEED 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1670-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1670-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1670-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1670-4 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
    CINNAMON 
    cinnamon injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1674
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB) CINNAMON 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1674-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1674-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1674-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1674-4 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
    CLOVES 
    cloves injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1678
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CLOVE (UNII: K48IKT5321) (CLOVE - UNII:K48IKT5321) CLOVE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1678-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1678-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1678-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1678-4 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
    DILL 
    dill injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1686
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DILL (UNII: Y05PC4JZRH) (DILL - UNII:Y05PC4JZRH) DILL 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1686-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1686-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1686-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1686-4 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
    GARLIC 
    garlic injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1690
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GARLIC (UNII: V1V998DC17) (GARLIC - UNII:V1V998DC17) GARLIC 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1690-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1690-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1690-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1690-4 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
    GINGER 
    ginger injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1694
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1694-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1694-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1694-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1694-4 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
    HORSERADISH 
    horseradish injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1698
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HORSERADISH (UNII: 8DS6G120HJ) (HORSERADISH - UNII:8DS6G120HJ) HORSERADISH 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1698-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1698-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1698-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1698-4 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
    LICORICE 
    licorice injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1702
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1702-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1702-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1702-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1702-4 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
    MUSTARD SEED 
    mustard seed injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1706
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MUSTARD SEED (UNII: 58RXI817UT) (MUSTARD SEED - UNII:58RXI817UT) MUSTARD SEED 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1706-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1706-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1706-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1706-4 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
    NUTMEG 
    nutmeg injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1710
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1710-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1710-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1710-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1710-4 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
    OREGANO 
    oregano injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1714
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OREGANO (UNII: 0E5AT8T16U) (OREGANO - UNII:0E5AT8T16U) OREGANO 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1714-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1714-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1714-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1714-4 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
    PAPRIKA 
    paprika injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1718
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PAPRIKA (UNII: X72Z47861V) (PAPRIKA - UNII:X72Z47861V) PAPRIKA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1718-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1718-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1718-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1718-4 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 PEPPER 
    white pepper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1722
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WHITE PEPPER (UNII: M29DW54Q9E) (WHITE PEPPER - UNII:M29DW54Q9E) WHITE PEPPER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1722-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1722-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1722-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1722-4 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
    PEPPERMINT 
    peppermint injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1726
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PEPPERMINT FLOWERING TOP (UNII: V95R5KMY2B) (PEPPERMINT FLOWERING TOP - UNII:V95R5KMY2B) PEPPERMINT FLOWERING TOP 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1726-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1726-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1726-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1726-4 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
    POPPYSEED 
    poppyseed injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1730
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POPPY SEED (UNII: 60RO23IR87) (POPPY SEED - UNII:60RO23IR87) POPPY SEED 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1730-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1730-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1730-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1730-4 10 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
    SAGE 
    sage injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1734
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALVIA OFFICINALIS (UNII: 065C5D077J) (SALVIA OFFICINALIS - UNII:065C5D077J) SALVIA OFFICINALIS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1734-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1734-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1734-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1734-4 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
    SESAME 
    sesame injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1738
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SESAME SEED (UNII: 7Y1255HVXR) (SESAME SEED - UNII:7Y1255HVXR) SESAME SEED 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1738-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1738-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1738-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1738-4 10 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
    SPEARMINT 
    spearmint injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1742
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SPEARMINT (UNII: J7I2T6IV1N) (SPEARMINT - UNII:J7I2T6IV1N) SPEARMINT 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1742-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1742-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1742-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1742-4 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
    THYME 
    thym injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1746
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GARDEN THYME (UNII: CW657OBU4N) (GARDEN THYME - UNII:CW657OBU4N) GARDEN THYME 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1746-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1746-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1746-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1746-4 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
    VANILLA 
    vanilla injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1750
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    VANILLA (UNII: Q74T35078H) (VANILLA - UNII:Q74T35078H) VANILLA 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1750-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1750-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1750-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1750-4 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
    WHEAT BRAN 
    wheat bran injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1754
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WHEAT BRAN (UNII: 6L966A1IMR) (WHEAT BRAN - UNII:6L966A1IMR) WHEAT BRAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1754-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1754-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1754-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1754-4 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 KIDNEY BEANS 
    white kidney beans injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1758
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO) KIDNEY BEAN 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1758-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1758-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1758-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1758-4 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 PEPPER 
    black pepper injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1766
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF) BLACK PEPPER 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1766-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1766-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1766-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1766-4 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
    HOPS 
    hops injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1774
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HOPS (UNII: 01G73H6H83) (HOPS - UNII:01G73H6H83) HOPS 0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    PHENOL (UNII: 339NCG44TV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:36987-1774-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1774-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1774-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1774-4 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 PEKOE TEA 
    orange pekoe tea injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-1654
    Route of Administration INTRADERMAL, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TEA LEAF (UNII: GH42T47V24) (TEA LEAF - UNII:GH42T47V24) TEA LEAF 0.05 g  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:36987-1654-1 5 mL in 1 VIAL, MULTI-DOSE
    2 NDC:36987-1654-2 10 mL in 1 VIAL, MULTI-DOSE
    3 NDC:36987-1654-3 30 mL in 1 VIAL, MULTI-DOSE
    4 NDC:36987-1654-4 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