Product NDC: | 68016-014 |
Proprietary Name: | PREMIER VALUE 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: | 68016-014 |
Labeler Name: | CHAIN DRUG CONSORTIUM, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120120 |
Package NDC: | 68016-014-79 |
Package Description: | 1 TUBE in 1 CARTON (68016-014-79) > 28 g in 1 TUBE |
NDC Code | 68016-014-79 |
Proprietary Name | PREMIER VALUE TOLNAFTATE ANTIFUNGAL |
Package Description | 1 TUBE in 1 CARTON (68016-014-79) > 28 g in 1 TUBE |
Product NDC | 68016-014 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TOLNAFTATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120120 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CHAIN DRUG CONSORTIUM, LLC |
Substance Name | TOLNAFTATE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes |