Product NDC: | 42432-019 |
Proprietary Name: | Kiss Fungi-Gone |
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: | 42432-019 |
Labeler Name: | Kiss Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121023 |
Package NDC: | 42432-019-06 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BOX (42432-019-06) > 30 mL in 1 BOTTLE, WITH APPLICATOR (42432-019-05) |
NDC Code | 42432-019-06 |
Proprietary Name | Kiss Fungi-Gone |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BOX (42432-019-06) > 30 mL in 1 BOTTLE, WITH APPLICATOR (42432-019-05) |
Product NDC | 42432-019 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tolnaftate |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20121023 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kiss Products, Inc. |
Substance Name | TOLNAFTATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |