Product NDC: | 42593-002 |
Proprietary Name: | Barielle Fungus Rx Maximum Strength Anti-Fungal |
Non Proprietary Name: | TOLNAFTATE |
Active Ingredient(s): | 1 mL/100mL & nbsp; TOLNAFTATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42593-002 |
Labeler Name: | Fisk Industries |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120101 |
Package NDC: | 42593-002-30 |
Package Description: | 1 BOTTLE in 1 PACKAGE (42593-002-30) > 30 mL in 1 BOTTLE |
NDC Code | 42593-002-30 |
Proprietary Name | Barielle Fungus Rx Maximum Strength Anti-Fungal |
Package Description | 1 BOTTLE in 1 PACKAGE (42593-002-30) > 30 mL in 1 BOTTLE |
Product NDC | 42593-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TOLNAFTATE |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20120101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Fisk Industries |
Substance Name | TOLNAFTATE |
Strength Number | 1 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |