Product NDC: | 41163-251 |
Proprietary Name: | EQUALINE 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: | 41163-251 |
Labeler Name: | SUPERVALU INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110928 |
Package NDC: | 41163-251-46 |
Package Description: | 1 TUBE in 1 CARTON (41163-251-46) > 14 g in 1 TUBE |
NDC Code | 41163-251-46 |
Proprietary Name | EQUALINE TOLNAFTATE ANTIFUNGAL |
Package Description | 1 TUBE in 1 CARTON (41163-251-46) > 14 g in 1 TUBE |
Product NDC | 41163-251 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TOLNAFTATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110928 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SUPERVALU INC |
Substance Name | TOLNAFTATE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes |