| 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 |