Product NDC: | 60193-100 |
Proprietary Name: | Woodwards Mycocide Clinical NS |
Non Proprietary Name: | TOLNAFTATE |
Active Ingredient(s): | 10 mg/mL & nbsp; TOLNAFTATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60193-100 |
Labeler Name: | Pacific Word Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130424 |
Package NDC: | 60193-100-06 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (60193-100-06) > 7.4 mL in 1 TUBE, WITH APPLICATOR |
NDC Code | 60193-100-06 |
Proprietary Name | Woodwards Mycocide Clinical NS |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (60193-100-06) > 7.4 mL in 1 TUBE, WITH APPLICATOR |
Product NDC | 60193-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TOLNAFTATE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20130424 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Pacific Word Corporation |
Substance Name | TOLNAFTATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |