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Fungicure
Fungicure - 52389-162-17 - (Tolnaftate)
Drug Information of Fungicure
| Product NDC: | 52389-162 |
| Proprietary Name: | Fungicure |
| Non Proprietary Name: | Tolnaftate |
| Active Ingredient(s): | 10 mg/g & nbsp; Tolnaftate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fungicure
| Product NDC: | 52389-162 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19941001 |
Package Information of Fungicure
| Package NDC: | 52389-162-17 |
| Package Description: | 17 g in 1 TUBE (52389-162-17) |
NDC Information of Fungicure
| NDC Code | 52389-162-17 |
| Proprietary Name | Fungicure |
| Package Description | 17 g in 1 TUBE (52389-162-17) |
| Product NDC | 52389-162 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tolnaftate |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19941001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
