Home
>
National Drug Code (NDC)
>
Barielle Professional Maximum Strength Fungus Rx Antifungal PRO
Barielle Professional Maximum Strength Fungus Rx Antifungal PRO - 42593-001-30 - (TOLNAFTATE)
Drug Information of Barielle Professional Maximum Strength Fungus Rx Antifungal PRO
| Product NDC: | 42593-001 |
| Proprietary Name: | Barielle Professional Maximum Strength Fungus Rx Antifungal PRO |
| 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) |
Labeler Information of Barielle Professional Maximum Strength Fungus Rx Antifungal PRO
| Product NDC: | 42593-001 |
| Labeler Name: | Fisk Industries |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120101 |
Package Information of Barielle Professional Maximum Strength Fungus Rx Antifungal PRO
| Package NDC: | 42593-001-30 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (42593-001-30) > 30 mL in 1 BOTTLE |
NDC Information of Barielle Professional Maximum Strength Fungus Rx Antifungal PRO
| NDC Code | 42593-001-30 |
| Proprietary Name | Barielle Professional Maximum Strength Fungus Rx Antifungal PRO |
| Package Description | 1 BOTTLE in 1 PACKAGE (42593-001-30) > 30 mL in 1 BOTTLE |
| Product NDC | 42593-001 |
| 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 |
