RED DELICIOUS APPLE - red delicious apple injection, solution 
APRICOT - apricot injection, solution 
AVOCADO - avocado injection, solution 
BANANA - banana injection, solution 
BLACKBERRY - blackberry injection, solution 
BLUEBERRY - blueberry injection, solution 
CANTALOUPE - cantaloupe injection, solution 
CHERRY BING - cherry bing injection, solution 
CRANBERRY - cranberry injection, solution 
DATE - date injection, solution 
FIG - fig injection, solution 
GRAPEFRUIT - grapefruit injection, solution 
HONEYDEW MELON - honeydew melon injection, solution 
LEMON - lemon injection, solution 
LIME - lime injection, solution 
ORANGE - orange injection, solution 
PEACH - peach injection, solution 
PEAR - pear injection, solution 
PINEAPPLE - pineapple injection, solution 
PLUM - plum injection, solution 
RASPBERRY - raspberry injection, solution 
STRAWBERRY - strawberry injection, solution 
TANGERINE - tangerine injection, solution 
WATERMELON - watermelon injection, solution 
ARTICHOKE - artichoke injection, solution 
ASPARAGUS - asparagus injection, solution 
RED KIDNEY BEANS - red kidney beans injection, solution 
LIMA BEANS - lima beans injection, solution 
NAVY BEANS - navy beans injection, solution 
STRING BEANS - string beans injection, solution 
BEET - beet injection, solution 
BROCCOLI - broccoli injection, solution 
KIWI - kiwi injection, solution 
BRUSSELS SPROUT - brussels sprout injection, solution 
CABBAGE - cabbage injection, solution 
CARROT - carrot injection, solution 
CAULIFLOWER - cauliflower injection, solution 
CELERY - celery injection, solution 
SWEET CORN - sweet corn injection, solution 
CUCUMBER - cucumber injection, solution 
EGG PLANT - egg plant injection, solution 
GREEN PEPPER - green pepper injection, solution 
LENTIL - lentil injection, solution 
ICEBERG LETTUCE - iceberg lettuce injection, solution 
MUSHROOM - mushroom injection, solution 
BLACK OLIVE - black olive injection, solution 
GREEN OLIVE - green olive injection, solution 
YELLOW ONION - yellow onion injection, solution 
PARSLEY - parsley injection, solution 
GREEN PEA - green pea injection, solution 
SWEET POTATO - sweet potato injection, solution 
WHITE POTATO - white potato injection, solution 
PUMPKIN - pumpkin injection, solution 
RADISH - radish injection, solution 
RHUBARB - rhubarb injection, solution 
SOYBEAN - soybean injection, solution 
SPINACH - spinach injection, solution 
SQUASH ZUCCHINI - squash zucchini injection, solution 
TOMATO - tomato injection, solution 
TURNIP - turnip injection, solution 
ALMOND - almond injection, solution 
BRAZIL NUT - brazil nut injection, solution 
CASHEW - cashew injection, solution 
COCONUT - coconut injection, solution 
ENGLISH WALNUT - english walnut injection, solution 
FILBERT - filbert injection, solution 
PEANUT - peanut injection, solution 
PECAN NUT - pecan nut injection, solution 
PISTACHIO - pistachio injection, solution 
BARLEY GRAIN - barley grain injection, solution 
BUCKWHEAT GRAIN - buckwheat grain injection, solution 
OAT GRAIN - oat grain injection, solution 
RICE GRAIN - rice grain injection, solution 
RYE GRAIN - rye grain injection, solution 
WHOLE WHEAT GRAIN - whole wheat grain injection, solution 
MACADAMIA NUT - macadamia nut injection, solution 
NECTARINE - nectarine injection, solution 
MANGO - mango injection, solution 
PAPAYA - papaya injection, solution 
LEEKS - leeks injection, solution 
OKRA - okra injection, solution 
PARSNIP - parsnip injection, solution 
CHICK PEA - chick pea injection, solution 
BLACKEYE PEA - blackeye pea injection, solution 
WATERCRESS - watercress injection, solution 
CORN GRAIN - corn grain injection, solution 
CACAO BEAN - cacao bean injection, solution 
COFFEE - coffee injection, solution 
MALT - malt injection, solution 
BREWERS YEAST - brewers yeast injection, solution 
ALLSPICE - allspice injection, solution 
BAY LEAF - bay leaf injection, solution 
CARAWAY SEED - caraway seed injection, solution 
CINNAMON - cinnamon injection, solution 
CLOVES - cloves injection, solution 
DILL - dill injection, solution 
GARLIC - garlic injection, solution 
GINGER - ginger injection, solution 
HORSERADISH - horseradish injection, solution 
LICORICE - licorice injection, solution 
MUSTARD SEED - mustard seed injection, solution 
NUTMEG - nutmeg injection, solution 
OREGANO - oregano injection, solution 
PAPRIKA - paprika injection, solution 
WHITE PEPPER - white pepper injection, solution 
PEPPERMINT - peppermint injection, solution 
POPPYSEED - poppyseed injection, solution 
SAGE - sage injection, solution 
SESAME - sesame injection, solution 
SPEARMINT - spearmint injection, solution 
THYME - thym injection, solution 
VANILLA - vanilla injection, solution 
WHEAT BRAN - wheat bran injection, solution 
WHITE KIDNEY BEANS - white kidney beans injection, solution 
BLACK PEPPER - black pepper injection, solution 
HOPS - hops injection, solution 
ORANGE PEKOE TEA - orange pekoe tea injection, solution 
Nelco Laboratories, Inc.

----------

Allergenic Extract

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)

REACTIONSYMBOLCRITERIA
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)

REACTIONSYMBOLCRITERIA
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.

STRENGTHDOSEVOLUME
Vial #110.05
1:100,000 w/v20.10
10 pnu/ml30.15
1 AU/ml40.20
1 BAU/ml50.30
60.40
70.50
Vial #280.05
1:10,000 w/v90.10
100 pnu/ml100.15
10 AU/ml110.20
10 BAU/ml120.30
130.40
140.50
Vial #3150.05
1:1,000 w/v160.10
1,000 pnu/ml170.15
100 AU/ml180.20
100 BAU/ml190.30
200.40
210.50
Vial #4220.05
1:100 w/v230.07
10,000 pnu/ml240.10
1,000 AU/ml250.15
1,000 BAU/ml260.20
270.25
Maintenance Refill280.25
1:100 w/v290.25
10,000 pnu/ml300.25
1,000 AU/ml310.25
1,000 BAU/ml320.25
subsequent doses330.25

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
RED DELICIOUS APPLE 
red delicious apple injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1282
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
APPLE (UNII: B423VGH5S9) (APPLE - UNII:B423VGH5S9) APPLE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1282-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1282-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1282-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1282-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
APRICOT 
apricot injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1286
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
APRICOT (UNII: 269CJD5GZ9) (APRICOT - UNII:269CJD5GZ9) APRICOT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
WATER (UNII: 059QF0KO0R)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1286-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1286-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1286-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1286-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
AVOCADO 
avocado injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1290
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOCADO (UNII: SDS87L369F) (AVOCADO - UNII:SDS87L369F) AVOCADO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1290-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1290-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1290-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1290-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BANANA 
banana injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1294
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BANANA (UNII: 4AJZ4765R9) (BANANA - UNII:4AJZ4765R9) BANANA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1294-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1294-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1294-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1294-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BLACKBERRY 
blackberry injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1298
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BLACKBERRY (UNII: 8A6OMU3I8L) (BLACKBERRY - UNII:8A6OMU3I8L) BLACKBERRY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1298-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1298-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1298-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1298-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BLUEBERRY 
blueberry injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1302
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BLUEBERRY (UNII: 253RUG1X1A) (BLUEBERRY - UNII:253RUG1X1A) BLUEBERRY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1302-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1302-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1302-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1302-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CANTALOUPE 
cantaloupe injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1306
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANTALOUPE (UNII: 8QF5D5H6UH) (CANTALOUPE - UNII:8QF5D5H6UH) CANTALOUPE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1306-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1306-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1306-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1306-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CHERRY BING 
cherry bing injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1310
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SOUR CHERRY (UNII: 1L29G6428X) (SOUR CHERRY - UNII:1L29G6428X) SOUR CHERRY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1310-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1310-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1310-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1310-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CRANBERRY 
cranberry injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1314
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CRANBERRY (UNII: 0MVO31Q3QS) (CRANBERRY - UNII:0MVO31Q3QS) CRANBERRY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1314-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1314-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1314-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1314-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
DATE 
date injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1318
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DATE (UNII: H3O7QI5HY7) (DATE - UNII:H3O7QI5HY7) DATE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1318-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1318-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1318-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1318-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
FIG 
fig injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1322
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FIG (UNII: TGD87RII2U) (FIG - UNII:TGD87RII2U) FIG0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1322-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1322-20.1 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1322-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1322-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
GRAPEFRUIT 
grapefruit injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1330
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GRAPEFRUIT (UNII: O82C39RR8C) (GRAPEFRUIT - UNII:O82C39RR8C) GRAPEFRUIT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1330-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1330-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1330-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1330-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
HONEYDEW MELON 
honeydew melon injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1334
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HONEYDEW MELON (UNII: RN8P45F92A) (HONEYDEW MELON - UNII:RN8P45F92A) HONEYDEW MELON0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1334-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1334-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1334-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1334-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
LEMON 
lemon injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1338
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEMON (UNII: 24RS0A988O) (LEMON - UNII:24RS0A988O) LEMON0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1338-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1338-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1338-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1338-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
LIME 
lime injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1342
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIME (CITRUS) (UNII: 8CZS546954) (LIME (CITRUS) - UNII:8CZS546954) LIME (CITRUS)0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1342-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1342-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1342-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1342-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ORANGE 
orange injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1346
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ORANGE (UNII: 5EVU04N5QU) (ORANGE - UNII:5EVU04N5QU) ORANGE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1346-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1346-230 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1346-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1346-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PEACH 
peach injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1350
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PEACH (UNII: 3OKE88I3QG) (PEACH - UNII:3OKE88I3QG) PEACH0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1350-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1350-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1350-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1350-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PEAR 
pear injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1354
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PEAR (UNII: 2ZN8DWC0YF) (PEAR - UNII:2ZN8DWC0YF) PEAR0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1354-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1354-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1354-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1354-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PINEAPPLE 
pineapple injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1358
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PINEAPPLE (UNII: 2A88ZO081O) (PINEAPPLE - UNII:2A88ZO081O) PINEAPPLE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1358-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1358-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1358-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1358-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PLUM 
plum injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1362
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PLUM (UNII: 67M3EQ6BE1) (PLUM - UNII:67M3EQ6BE1) PLUM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1362-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1362-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1362-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1362-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
RASPBERRY 
raspberry injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1366
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RASPBERRY (UNII: 4N14V5R27W) (RASPBERRY - UNII:4N14V5R27W) RASPBERRY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1366-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1366-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1366-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1366-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
STRAWBERRY 
strawberry injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1370
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STRAWBERRY (UNII: 4J2TY8Y81V) (STRAWBERRY - UNII:4J2TY8Y81V) STRAWBERRY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1370-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1370-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1370-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1370-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
TANGERINE 
tangerine injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1374
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TANGERINE (UNII: KH3E3096OO) (TANGERINE - UNII:KH3E3096OO) TANGERINE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1374-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1374-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1374-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1374-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WATERMELON 
watermelon injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1378
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATERMELON (UNII: 231473QB6R) (WATERMELON - UNII:231473QB6R) WATERMELON0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1378-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1378-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1378-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1378-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ARTICHOKE 
artichoke injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1382
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARTICHOKE (UNII: 4F3W47PLBE) (ARTICHOKE - UNII:4F3W47PLBE) ARTICHOKE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1382-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1382-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1382-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1382-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ASPARAGUS 
asparagus injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1386
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPARAGUS (UNII: Z1EJP3037Z) (ASPARAGUS - UNII:Z1EJP3037Z) ASPARAGUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1386-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1386-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1386-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1386-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
RED KIDNEY BEANS 
red kidney beans injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1390
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO) KIDNEY BEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1390-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1390-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1390-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1390-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
LIMA BEANS 
lima beans injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1394
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIMA BEAN (UNII: 112YH1ZMX2) (LIMA BEAN - UNII:112YH1ZMX2) LIMA BEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1394-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1394-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1394-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1394-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
NAVY BEANS 
navy beans injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1398
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO) KIDNEY BEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1398-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1398-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1398-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1398-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
STRING BEANS 
string beans injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1402
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STRING BEAN (UNII: N9D69B2Q7Y) (STRING BEAN - UNII:N9D69B2Q7Y) STRING BEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1402-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1402-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1402-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1402-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BEET 
beet injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1406
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BEET (UNII: N487KM8COK) (BEET - UNII:N487KM8COK) BEET0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1406-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1406-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1406-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1406-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BROCCOLI 
broccoli injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1410
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BROCCOLI (UNII: UOI4FT57BZ) (BROCCOLI - UNII:UOI4FT57BZ) BROCCOLI0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1410-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1410-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1410-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1410-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
KIWI 
kiwi injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1414
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KIWI FRUIT (UNII: 71ES77LGJC) (KIWI FRUIT - UNII:71ES77LGJC) KIWI FRUIT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1414-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1414-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1414-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1414-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BRUSSELS SPROUT 
brussels sprout injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1418
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BRUSSELS SPROUT (UNII: KHX46H31F8) (BRUSSELS SPROUT - UNII:KHX46H31F8) BRUSSELS SPROUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1418-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1418-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1418-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1418-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CABBAGE 
cabbage injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1422
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CABBAGE (UNII: GW0W1Y9I97) (CABBAGE - UNII:GW0W1Y9I97) CABBAGE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1422-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1422-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1422-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1422-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CARROT 
carrot injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1426
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARROT (UNII: L56Z1JK48B) (CARROT - UNII:L56Z1JK48B) CARROT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1426-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1426-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1426-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1426-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CAULIFLOWER 
cauliflower injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1430
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAULIFLOWER (UNII: 138LUT2DWV) (CAULIFLOWER - UNII:138LUT2DWV) CAULIFLOWER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1430-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1430-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1430-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1430-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CELERY 
celery injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1434
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CELERY (UNII: 44IDY6DTKX) (CELERY - UNII:44IDY6DTKX) CELERY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1434-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1434-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1434-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1434-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SWEET CORN 
sweet corn injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1438
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O) CORN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1438-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1438-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1438-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1438-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CUCUMBER 
cucumber injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1442
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CUCUMBER (UNII: YY7C30VXJT) (CUCUMBER - UNII:YY7C30VXJT) CUCUMBER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1442-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1442-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1442-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1442-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
EGG PLANT 
egg plant injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1446
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EGGPLANT (UNII: W5K7RAS4VK) (EGGPLANT - UNII:W5K7RAS4VK) EGGPLANT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1446-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1446-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1446-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1446-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
GREEN PEPPER 
green pepper injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1450
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GREEN BELL PEPPER (UNII: 4J4DOU3HEK) (GREEN BELL PEPPER - UNII:4J4DOU3HEK) GREEN BELL PEPPER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1450-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1450-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1450-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1450-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
LENTIL 
lentil injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1454
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LENTIL (UNII: 6O38V6B52O) (LENTIL - UNII:6O38V6B52O) LENTIL0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1454-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1454-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1454-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1454-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ICEBERG LETTUCE 
iceberg lettuce injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1458
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LETTUCE (UNII: 5PO6NN3RRJ) (LETTUCE - UNII:5PO6NN3RRJ) LETTUCE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1458-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1458-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1458-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1458-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
MUSHROOM 
mushroom injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1462
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CULTIVATED MUSHROOM (UNII: 54C8E6W6JY) (CULTIVATED MUSHROOM - UNII:54C8E6W6JY) CULTIVATED MUSHROOM0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1462-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1462-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1462-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1462-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BLACK OLIVE 
black olive injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1466
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BLACK OLIVE (UNII: 2M6QWV94OC) (BLACK OLIVE - UNII:2M6QWV94OC) BLACK OLIVE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1466-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1466-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1466-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1466-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
GREEN OLIVE 
green olive injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1470
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GREEN OLIVE (UNII: 6HD2W46UEG) (GREEN OLIVE - UNII:6HD2W46UEG) GREEN OLIVE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1470-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1470-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1470-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1470-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
YELLOW ONION 
yellow onion injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1474
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1474-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1474-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1474-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1474-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PARSLEY 
parsley injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1478
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PARSLEY (UNII: 58FMD0Q0EV) (PARSLEY - UNII:58FMD0Q0EV) PARSLEY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1478-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1478-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1478-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1478-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
GREEN PEA 
green pea injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1482
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PEA (UNII: W4X7H8GYFM) (PEA - UNII:W4X7H8GYFM) PEA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1482-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1482-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1482-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1482-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SWEET POTATO 
sweet potato injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1486
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SWEET POTATO (UNII: M9WGG9Z9GK) (SWEET POTATO - UNII:M9WGG9Z9GK) SWEET POTATO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1486-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1486-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1486-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1486-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WHITE POTATO 
white potato injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1490
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTATO (UNII: CFE1S8DYWD) (POTATO - UNII:CFE1S8DYWD) POTATO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1490-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1490-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1490-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1490-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PUMPKIN 
pumpkin injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1494
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO (UNII: SYW0QUB89Y) (ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO - UNII:SYW0QUB89Y) ALLERGENIC EXTRACT- PUMPKIN CUCURBITA PEPO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1494-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1494-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1494-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1494-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
RADISH 
radish injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1498
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RAPHANUS SATIVUS (UNII: 86R5J6D01D) (RAPHANUS SATIVUS - UNII:86R5J6D01D) RAPHANUS SATIVUS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1498-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1498-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1498-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1498-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
RHUBARB 
rhubarb injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1502
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RHUBARB (UNII: G280W4MW6E) (RHUBARB - UNII:G280W4MW6E) RHUBARB0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1502-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1502-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1502-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1502-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SOYBEAN 
soybean injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1506
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SOYBEAN (UNII: L7HT8F1ZOD) (SOYBEAN - UNII:L7HT8F1ZOD) SOYBEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1506-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1506-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1506-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1506-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SPINACH 
spinach injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1510
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SPINACH (UNII: 6WO75C6WVB) (SPINACH - UNII:6WO75C6WVB) SPINACH0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1510-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1510-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1510-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1510-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SQUASH ZUCCHINI 
squash zucchini injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1514
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SQUASH (UNII: 9961HBA483) (SQUASH - UNII:9961HBA483) SQUASH0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1514-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1514-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1514-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1514-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
TOMATO 
tomato injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1518
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOMATO (UNII: Z4KHF2C175) (TOMATO - UNII:Z4KHF2C175) TOMATO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1518-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1518-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1518-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1518-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
TURNIP 
turnip injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1522
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TURNIP (UNII: Z38C7FBM49) (TURNIP - UNII:Z38C7FBM49) TURNIP0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1522-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1522-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1522-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1522-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ALMOND 
almond injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1526
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALMOND (UNII: 3Z252A2K9G) (ALMOND - UNII:3Z252A2K9G) ALMOND0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1526-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1526-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1526-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1526-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BRAZIL NUT 
brazil nut injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1530
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BRAZIL NUT (UNII: XKR79OET1K) (BRAZIL NUT - UNII:XKR79OET1K) BRAZIL NUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1530-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1530-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1530-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1530-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CASHEW 
cashew injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1534
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CASHEW (UNII: 3H5U5CX7KO) (CASHEW - UNII:3H5U5CX7KO) CASHEW0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1534-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1534-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1534-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1534-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
COCONUT 
coconut injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1538
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCONUT (UNII: 3RT3536DHY) (COCONUT - UNII:3RT3536DHY) COCONUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1538-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1538-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1538-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1538-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ENGLISH WALNUT 
english walnut injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1542
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ENGLISH WALNUT (UNII: 1V3SHR7QB7) (ENGLISH WALNUT - UNII:1V3SHR7QB7) ENGLISH WALNUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1542-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1542-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1542-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1542-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
FILBERT 
filbert injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1546
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HAZELNUT (UNII: IW0OM96F6O) (HAZELNUT - UNII:IW0OM96F6O) HAZELNUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1546-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1546-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1546-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1546-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PEANUT 
peanut injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1550
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PEANUT (UNII: QE1QX6B99R) (PEANUT - UNII:QE1QX6B99R) PEANUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1550-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1550-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1550-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1550-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PECAN NUT 
pecan nut injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1554
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PECAN (UNII: F14P91GB5F) (PECAN - UNII:F14P91GB5F) PECAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1554-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1554-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1554-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1554-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PISTACHIO 
pistachio injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1558
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PISTACHIO (UNII: 6815CPT6ZJ) (PISTACHIO - UNII:6815CPT6ZJ) PISTACHIO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1558-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1558-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1558-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1558-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BARLEY GRAIN 
barley grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1562
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BARLEY (UNII: 5PWM7YLI7R) (BARLEY - UNII:5PWM7YLI7R) BARLEY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1562-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1562-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1562-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1562-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BUCKWHEAT GRAIN 
buckwheat grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1566
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3) BUCKWHEAT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1566-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1566-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1566-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1566-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
OAT GRAIN 
oat grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1570
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OAT (UNII: Z6J799EAJK) (OAT - UNII:Z6J799EAJK) OAT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1570-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1570-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1570-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1570-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
RICE GRAIN 
rice grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1574
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RICE (UNII: 659G217HPG) (RICE - UNII:659G217HPG) RICE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1574-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1574-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1574-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1574-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
RYE GRAIN 
rye grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1578
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RYE (UNII: 0R4AQI398X) (RYE - UNII:0R4AQI398X) RYE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1578-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1578-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1578-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1578-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WHOLE WHEAT GRAIN 
whole wheat grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1582
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WHEAT (UNII: 4J2I0SN84Y) (WHEAT - UNII:4J2I0SN84Y) WHEAT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1582-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1582-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1582-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1582-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
MACADAMIA NUT 
macadamia nut injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1586
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MACADAMIA NUT (UNII: Y5432RGW8N) (MACADAMIA NUT - UNII:Y5432RGW8N) MACADAMIA NUT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1586-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1586-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1586-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1586-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
NECTARINE 
nectarine injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1590
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NECTARINE (UNII: 65KD9TD4C3) (NECTARINE - UNII:65KD9TD4C3) NECTARINE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1590-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1590-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1590-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1590-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
MANGO 
mango injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1594
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MANGO (UNII: I629I3NR86) (MANGO - UNII:I629I3NR86) MANGO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1594-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1594-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1594-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1594-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PAPAYA 
papaya injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1598
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAPAYA (UNII: KU94FIY6JB) (PAPAYA - UNII:KU94FIY6JB) PAPAYA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1598-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1598-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1598-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1598-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
LEEKS 
leeks injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1602
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEEK (UNII: RCU76P419D) (LEEK - UNII:RCU76P419D) LEEK0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1602-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1602-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1602-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1602-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
OKRA 
okra injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1606
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OKRA (UNII: 51ME2L7STL) (OKRA - UNII:51ME2L7STL) OKRA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1606-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1606-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1606-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1606-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PARSNIP 
parsnip injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1610
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PARSNIP (UNII: L2V28YP49S) (PARSNIP - UNII:L2V28YP49S) PARSNIP0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1610-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1610-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1610-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1610-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CHICK PEA 
chick pea injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1614
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHICKPEA (UNII: N91637DNW9) (CHICKPEA - UNII:N91637DNW9) CHICKPEA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1614-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1614-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1614-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1614-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BLACKEYE PEA 
blackeye pea injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1618
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BLACK-EYED PEA (UNII: 786YV7B602) (BLACK-EYED PEA - UNII:786YV7B602) BLACK-EYED PEA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1618-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1618-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1618-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1618-410 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WATERCRESS 
watercress injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1622
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATERCRESS (UNII: K5877MW0LE) (WATERCRESS - UNII:K5877MW0LE) WATERCRESS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1622-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1622-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1622-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1622-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CORN GRAIN 
corn grain injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1626
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CORN (UNII: 0N8672707O) (CORN - UNII:0N8672707O) CORN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1626-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1626-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1626-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1626-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CACAO BEAN 
cacao bean injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1630
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHOCOLATE (UNII: D9108TZ9KG) (CHOCOLATE - UNII:D9108TZ9KG) CHOCOLATE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1630-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1630-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1630-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1630-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
COFFEE 
coffee injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1634
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARABICA COFFEE BEAN (UNII: 3SW678MX72) (ARABICA COFFEE BEAN - UNII:3SW678MX72) ARABICA COFFEE BEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1634-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1634-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1634-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1634-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
MALT 
malt injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1650
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MALT EXTRACT, BARLEY (UNII: R3NBG8914U) (MALT EXTRACT, BARLEY - UNII:R3NBG8914U) MALT EXTRACT, BARLEY0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1650-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1650-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1650-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1650-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BREWERS YEAST 
brewers yeast injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1658
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (SACCHAROMYCES CEREVISIAE - UNII:978D8U419H) SACCHAROMYCES CEREVISIAE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1658-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1658-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1658-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1658-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ALLSPICE 
allspice injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1662
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLSPICE (UNII: I5GZG55B36) (ALLSPICE - UNII:I5GZG55B36) ALLSPICE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1662-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1662-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1662-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1662-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BAY LEAF 
bay leaf injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1666
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LAURUS NOBILIS (UNII: 247012Z29Q) (LAURUS NOBILIS - UNII:247012Z29Q) LAURUS NOBILIS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1666-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1666-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1666-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1666-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CARAWAY SEED 
caraway seed injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1670
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARAWAY SEED (UNII: W2FH8O2BBE) (CARAWAY SEED - UNII:W2FH8O2BBE) CARAWAY SEED0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1670-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1670-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1670-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1670-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CINNAMON 
cinnamon injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1674
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB) CINNAMON0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1674-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1674-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1674-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1674-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
CLOVES 
cloves injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1678
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLOVE (UNII: K48IKT5321) (CLOVE - UNII:K48IKT5321) CLOVE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1678-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1678-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1678-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1678-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
DILL 
dill injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1686
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DILL (UNII: Y05PC4JZRH) (DILL - UNII:Y05PC4JZRH) DILL0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1686-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1686-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1686-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1686-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
GARLIC 
garlic injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1690
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GARLIC (UNII: V1V998DC17) (GARLIC - UNII:V1V998DC17) GARLIC0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1690-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1690-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1690-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1690-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
GINGER 
ginger injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1694
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1694-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1694-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1694-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1694-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
HORSERADISH 
horseradish injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1698
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HORSERADISH (UNII: 8DS6G120HJ) (HORSERADISH - UNII:8DS6G120HJ) HORSERADISH0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1698-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1698-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1698-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1698-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
LICORICE 
licorice injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1702
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1702-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1702-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1702-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1702-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
MUSTARD SEED 
mustard seed injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1706
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MUSTARD SEED (UNII: 58RXI817UT) (MUSTARD SEED - UNII:58RXI817UT) MUSTARD SEED0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1706-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1706-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1706-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1706-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
NUTMEG 
nutmeg injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1710
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NUTMEG (UNII: AEE24M3MQ9) (NUTMEG - UNII:AEE24M3MQ9) NUTMEG0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1710-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1710-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1710-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1710-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
OREGANO 
oregano injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1714
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OREGANO (UNII: 0E5AT8T16U) (OREGANO - UNII:0E5AT8T16U) OREGANO0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1714-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1714-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1714-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1714-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PAPRIKA 
paprika injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1718
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAPRIKA (UNII: X72Z47861V) (PAPRIKA - UNII:X72Z47861V) PAPRIKA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1718-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1718-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1718-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1718-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WHITE PEPPER 
white pepper injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1722
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WHITE PEPPER (UNII: M29DW54Q9E) (WHITE PEPPER - UNII:M29DW54Q9E) WHITE PEPPER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1722-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1722-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1722-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1722-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
PEPPERMINT 
peppermint injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1726
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PEPPERMINT FLOWERING TOP (UNII: V95R5KMY2B) (PEPPERMINT FLOWERING TOP - UNII:V95R5KMY2B) PEPPERMINT FLOWERING TOP0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1726-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1726-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1726-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1726-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
POPPYSEED 
poppyseed injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1730
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POPPY SEED (UNII: 60RO23IR87) (POPPY SEED - UNII:60RO23IR87) POPPY SEED0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1730-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1730-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1730-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1730-410 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SAGE 
sage injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1734
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALVIA OFFICINALIS (UNII: 065C5D077J) (SALVIA OFFICINALIS - UNII:065C5D077J) SALVIA OFFICINALIS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1734-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1734-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1734-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1734-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SESAME 
sesame injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1738
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SESAME SEED (UNII: 7Y1255HVXR) (SESAME SEED - UNII:7Y1255HVXR) SESAME SEED0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1738-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1738-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1738-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1738-410 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
SPEARMINT 
spearmint injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1742
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SPEARMINT (UNII: J7I2T6IV1N) (SPEARMINT - UNII:J7I2T6IV1N) SPEARMINT0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1742-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1742-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1742-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1742-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
THYME 
thym injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1746
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GARDEN THYME (UNII: CW657OBU4N) (GARDEN THYME - UNII:CW657OBU4N) GARDEN THYME0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1746-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1746-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1746-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1746-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
VANILLA 
vanilla injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1750
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VANILLA (UNII: Q74T35078H) (VANILLA - UNII:Q74T35078H) VANILLA0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1750-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1750-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1750-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1750-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WHEAT BRAN 
wheat bran injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1754
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WHEAT BRAN (UNII: 6L966A1IMR) (WHEAT BRAN - UNII:6L966A1IMR) WHEAT BRAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1754-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1754-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1754-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1754-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
WHITE KIDNEY BEANS 
white kidney beans injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1758
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KIDNEY BEAN (UNII: M98C8416QO) (KIDNEY BEAN - UNII:M98C8416QO) KIDNEY BEAN0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1758-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1758-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1758-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1758-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
BLACK PEPPER 
black pepper injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1766
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BLACK PEPPER (UNII: KM66971LVF) (BLACK PEPPER - UNII:KM66971LVF) BLACK PEPPER0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1766-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1766-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1766-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1766-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
HOPS 
hops injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1774
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOPS (UNII: 01G73H6H83) (HOPS - UNII:01G73H6H83) HOPS0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
PHENOL (UNII: 339NCG44TV)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1774-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1774-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1774-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1774-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
ORANGE PEKOE TEA 
orange pekoe tea injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:36987-1654
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TEA LEAF (UNII: GH42T47V24) (TEA LEAF - UNII:GH42T47V24) TEA LEAF0.05 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
WATER (UNII: 059QF0KO0R)  
PHENOL (UNII: 339NCG44TV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36987-1654-15 mL in 1 VIAL, MULTI-DOSE
2NDC:36987-1654-210 mL in 1 VIAL, MULTI-DOSE
3NDC:36987-1654-330 mL in 1 VIAL, MULTI-DOSE
4NDC:36987-1654-450 mL in 1 VIAL, MULTI-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
BLABLA10219208/29/1972
Labeler - Nelco Laboratories, Inc. (054980867)
Registrant - Nelco Laboratories, Inc. (054980867)
Establishment
NameAddressID/FEIBusiness Operations
Nelco Laboratories, Inc.054980867manufacture

Revised: 12/2009
Document Id: dec580ea-73db-4658-9de1-440c19bb42b7
Set id: b65366b5-55ea-49dc-8011-8ef9af097291
Version: 3
Effective Time: 20091209
 
Nelco Laboratories, Inc.