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Candida Albicans Remedy - 43742-0173-1 - (Candida Albicans)

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Drug Information of Candida Albicans Remedy

Product NDC: 43742-0173
Proprietary Name: Candida Albicans Remedy
Non Proprietary Name: Candida Albicans
Active Ingredient(s): 15    [hp_X]/mL & nbsp;   Candida Albicans
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Candida Albicans Remedy

Product NDC: 43742-0173
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121031

Package Information of Candida Albicans Remedy

Package NDC: 43742-0173-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43742-0173-1)

NDC Information of Candida Albicans Remedy

NDC Code 43742-0173-1
Proprietary Name Candida Albicans Remedy
Package Description 30 mL in 1 BOTTLE, DROPPER (43742-0173-1)
Product NDC 43742-0173
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candida Albicans
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121031
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Deseret Biologicals, Inc.
Substance Name CANDIDA ALBICANS
Strength Number 15
Strength Unit [hp_X]/mL
Pharmaceutical Classes Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE]

Complete Information of Candida Albicans Remedy


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