| 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 |