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Bonogen Activator - 50653-3001-2 - (BIOTIN)

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Drug Information of Bonogen Activator

Product NDC: 50653-3001
Proprietary Name: Bonogen Activator
Non Proprietary Name: BIOTIN
Active Ingredient(s): .002    mL/mL & nbsp;   BIOTIN
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Bonogen Activator

Product NDC: 50653-3001
Labeler Name: Bonogen Co., Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100425

Package Information of Bonogen Activator

Package NDC: 50653-3001-2
Package Description: 150 mL in 1 BOTTLE, WITH APPLICATOR (50653-3001-2)

NDC Information of Bonogen Activator

NDC Code 50653-3001-2
Proprietary Name Bonogen Activator
Package Description 150 mL in 1 BOTTLE, WITH APPLICATOR (50653-3001-2)
Product NDC 50653-3001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BIOTIN
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100425
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Bonogen Co., Ltd
Substance Name BIOTIN
Strength Number .002
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Bonogen Activator


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