Product NDC: | 66854-007 |
Proprietary Name: | SPAI-SONS |
Non Proprietary Name: | BIOTIN |
Active Ingredient(s): | .01 mg/100mL & nbsp; BIOTIN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66854-007 |
Labeler Name: | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120806 |
Package NDC: | 66854-007-02 |
Package Description: | 10 mL in 1 BOTTLE (66854-007-02) |
NDC Code | 66854-007-02 |
Proprietary Name | SPAI-SONS |
Package Description | 10 mL in 1 BOTTLE (66854-007-02) |
Product NDC | 66854-007 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | BIOTIN |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120806 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS |
Substance Name | BIOTIN |
Strength Number | .01 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |