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