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 |