 
                        | 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: | 76348-401-02 | 
| Package Description: | 11.5 mL in 1 BOX (76348-401-02) | 
| NDC Code | 76348-401-02 | 
| Proprietary Name | Molecular AF | 
| Package Description | 11.5 mL in 1 BOX (76348-401-02) | 
| 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 |