Product NDC: | 57896-199 |
Proprietary Name: | TOLNAFTATE ANTIFUNGAL |
Non Proprietary Name: | TOLNAFTATE |
Active Ingredient(s): | 1 g/100g & nbsp; TOLNAFTATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57896-199 |
Labeler Name: | Geri-Care Pharmaceuticals, Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110801 |
Package NDC: | 57896-199-45 |
Package Description: | 45 g in 1 BOTTLE, DISPENSING (57896-199-45) |
NDC Code | 57896-199-45 |
Proprietary Name | TOLNAFTATE ANTIFUNGAL |
Package Description | 45 g in 1 BOTTLE, DISPENSING (57896-199-45) |
Product NDC | 57896-199 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TOLNAFTATE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20110801 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Geri-Care Pharmaceuticals, Corp |
Substance Name | TOLNAFTATE |
Strength Number | 1 |
Strength Unit | g/100g |
Pharmaceutical Classes |