| Product NDC: | 37205-344 |
| Proprietary Name: | Leader Medicated |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 10 mg/g & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37205-344 |
| Labeler Name: | Cardinal Health Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080315 |
| Package NDC: | 37205-344-66 |
| Package Description: | 130 g in 1 CAN (37205-344-66) |
| NDC Code | 37205-344-66 |
| Proprietary Name | Leader Medicated |
| Package Description | 130 g in 1 CAN (37205-344-66) |
| Product NDC | 37205-344 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | AEROSOL, POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20080315 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cardinal Health Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |