| Product NDC: | 63736-819 |
| Proprietary Name: | Ting |
| Non Proprietary Name: | Tolnaftate |
| Active Ingredient(s): | 1.28 g/128g & nbsp; Tolnaftate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63736-819 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090727 |
| Package NDC: | 63736-819-05 |
| Package Description: | 128 g in 1 CAN (63736-819-05) |
| NDC Code | 63736-819-05 |
| Proprietary Name | Ting |
| Package Description | 128 g in 1 CAN (63736-819-05) |
| Product NDC | 63736-819 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tolnaftate |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20090727 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | TOLNAFTATE |
| Strength Number | 1.28 |
| Strength Unit | g/128g |
| Pharmaceutical Classes |