| Product NDC: | 49406-003 |
| Proprietary Name: | Formula 3 |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49406-003 |
| Labeler Name: | The Tetra Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121030 |
| Package NDC: | 49406-003-15 |
| Package Description: | 15 mL in 1 BOTTLE (49406-003-15) |
| NDC Code | 49406-003-15 |
| Proprietary Name | Formula 3 |
| Package Description | 15 mL in 1 BOTTLE (49406-003-15) |
| Product NDC | 49406-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121030 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Tetra Corporation |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |