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Allergy Desensitization - 68770-120-15 - (Onion, Apis Mellifera, Schoenocaulon Officinale Seed, Euphrasia Stricta)

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Drug Information of Allergy Desensitization

Product NDC: 68770-120
Proprietary Name: Allergy Desensitization
Non Proprietary Name: Onion, Apis Mellifera, Schoenocaulon Officinale Seed, Euphrasia Stricta
Active Ingredient(s): 6; 4; 6; 6    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Onion, Apis Mellifera, Schoenocaulon Officinale Seed, Euphrasia Stricta
Administration Route(s): INTRAOCULAR
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Allergy Desensitization

Product NDC: 68770-120
Labeler Name: Natural Ophthalmics, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20040601

Package Information of Allergy Desensitization

Package NDC: 68770-120-15
Package Description: 15 mL in 1 BOTTLE, DROPPER (68770-120-15)

NDC Information of Allergy Desensitization

NDC Code 68770-120-15
Proprietary Name Allergy Desensitization
Package Description 15 mL in 1 BOTTLE, DROPPER (68770-120-15)
Product NDC 68770-120
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Onion, Apis Mellifera, Schoenocaulon Officinale Seed, Euphrasia Stricta
Dosage Form Name LIQUID
Route Name INTRAOCULAR
Start Marketing Date 20040601
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Ophthalmics, Inc
Substance Name APIS MELLIFERA; EUPHRASIA STRICTA; ONION; SCHOENOCAULON OFFICINALE SEED
Strength Number 6; 4; 6; 6
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Allergy Desensitization


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