| Product NDC: | 41163-251 |
| Proprietary Name: | EQUALINE TOLNAFTATE ANTIFUNGAL |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 10 mg/g & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 41163-251 |
| Labeler Name: | SUPERVALU INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110928 |
| Package NDC: | 41163-251-46 |
| Package Description: | 1 TUBE in 1 CARTON (41163-251-46) > 14 g in 1 TUBE |
| NDC Code | 41163-251-46 |
| Proprietary Name | EQUALINE TOLNAFTATE ANTIFUNGAL |
| Package Description | 1 TUBE in 1 CARTON (41163-251-46) > 14 g in 1 TUBE |
| Product NDC | 41163-251 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110928 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SUPERVALU INC |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |