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Candida Combo - 43857-0011-1 - (Candida Albicans)

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Drug Information of Candida Combo

Product NDC: 43857-0011
Proprietary Name: Candida Combo
Non Proprietary Name: Candida Albicans
Active Ingredient(s): 12    [hp_X]/mL & nbsp;   Candida Albicans
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Candida Combo

Product NDC: 43857-0011
Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130116

Package Information of Candida Combo

Package NDC: 43857-0011-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43857-0011-1)

NDC Information of Candida Combo

NDC Code 43857-0011-1
Proprietary Name Candida Combo
Package Description 30 mL in 1 BOTTLE, DROPPER (43857-0011-1)
Product NDC 43857-0011
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Candida Albicans
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130116
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name BioActive Nutritional, Inc.
Substance Name CANDIDA ALBICANS
Strength Number 12
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Candida Combo


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