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TK-NAX
TK-NAX - 66854-020-01 - (BIOTIN)
Drug Information of TK-NAX
| Product NDC: | 66854-020 |
| Proprietary Name: | TK-NAX |
| Non Proprietary Name: | BIOTIN |
| Active Ingredient(s): | .01 mL/100mL & nbsp; BIOTIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TK-NAX
| Product NDC: | 66854-020 |
| Labeler Name: | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120630 |
Package Information of TK-NAX
| Package NDC: | 66854-020-01 |
| Package Description: | 70 mL in 1 JAR (66854-020-01) |
NDC Information of TK-NAX
| NDC Code | 66854-020-01 |
| Proprietary Name | TK-NAX |
| Package Description | 70 mL in 1 JAR (66854-020-01) |
| Product NDC | 66854-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BIOTIN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120630 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
| Substance Name | BIOTIN |
| Strength Number | .01 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
