Product NDC: | 63736-051 |
Proprietary Name: | Ting |
Non Proprietary Name: | Tolnaftate |
Active Ingredient(s): | 100 mg/g & nbsp; Tolnaftate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63736-051 |
Labeler Name: | Insight Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090608 |
Package NDC: | 63736-051-01 |
Package Description: | 1 TUBE in 1 BOX (63736-051-01) > 14 g in 1 TUBE |
NDC Code | 63736-051-01 |
Proprietary Name | Ting |
Package Description | 1 TUBE in 1 BOX (63736-051-01) > 14 g in 1 TUBE |
Product NDC | 63736-051 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tolnaftate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20090608 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Insight Pharmaceuticals |
Substance Name | TOLNAFTATE |
Strength Number | 100 |
Strength Unit | mg/g |
Pharmaceutical Classes |