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Antifungal
Antifungal - 47682-229-35 - (tolnaftate)
Drug Information of Antifungal
| Product NDC: | 47682-229 |
| Proprietary Name: | 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) |
Labeler Information of Antifungal
| Product NDC: | 47682-229 |
| Labeler Name: | Unifirst First Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20020630 |
Package Information of Antifungal
| Package NDC: | 47682-229-35 |
| Package Description: | 144 PACKET in 1 BOX (47682-229-35) > .9 g in 1 PACKET |
NDC Information of Antifungal
| NDC Code | 47682-229-35 |
| Proprietary Name | Antifungal |
| Package Description | 144 PACKET in 1 BOX (47682-229-35) > .9 g in 1 PACKET |
| Product NDC | 47682-229 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | tolnaftate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20020630 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Unifirst First Aid Corporation |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
