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CLARUS Antifungal
CLARUS Antifungal - 44577-001-01 - (TOLNAFTATE)
Drug Information of CLARUS Antifungal
| Product NDC: | 44577-001 |
| Proprietary Name: | CLARUS Antifungal |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 1 g/100g & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLARUS Antifungal
| Product NDC: | 44577-001 |
| Labeler Name: | Clinical Therapeutic Solutions |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120607 |
Package Information of CLARUS Antifungal
| Package NDC: | 44577-001-01 |
| Package Description: | 45 g in 1 TUBE (44577-001-01) |
NDC Information of CLARUS Antifungal
| NDC Code | 44577-001-01 |
| Proprietary Name | CLARUS Antifungal |
| Package Description | 45 g in 1 TUBE (44577-001-01) |
| Product NDC | 44577-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120607 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Clinical Therapeutic Solutions |
| Substance Name | TOLNAFTATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
