Product NDC: | 76348-401 |
Proprietary Name: | Molecular AF |
Non Proprietary Name: | Tolnaftate |
Active Ingredient(s): | .01 mg/mL & nbsp; Tolnaftate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OIL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76348-401 |
Labeler Name: | Renu Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110701 |
Package NDC: | 76348-401-01 |
Package Description: | 11.5 mL in 1 BOTTLE (76348-401-01) |
NDC Code | 76348-401-01 |
Proprietary Name | Molecular AF |
Package Description | 11.5 mL in 1 BOTTLE (76348-401-01) |
Product NDC | 76348-401 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tolnaftate |
Dosage Form Name | OIL |
Route Name | TOPICAL |
Start Marketing Date | 20110701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Renu Laboratories, Inc. |
Substance Name | TOLNAFTATE |
Strength Number | .01 |
Strength Unit | mg/mL |
Pharmaceutical Classes |