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Clarifoam EF
Clarifoam EF - 16781-154-96 - (SULFUR,SULFACETAMIDE SODIUM)
Drug Information of Clarifoam EF
| Product NDC: | 16781-154 |
| Proprietary Name: | Clarifoam EF |
| Non Proprietary Name: | SULFUR,SULFACETAMIDE SODIUM |
| Active Ingredient(s): | 10; 5 g/100g; g/100g & nbsp; SULFUR,SULFACETAMIDE SODIUM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clarifoam EF
| Product NDC: | 16781-154 |
| Labeler Name: | Onset Dermatologics LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070601 |
Package Information of Clarifoam EF
| Package NDC: | 16781-154-96 |
| Package Description: | 100 g in 1 CAN (16781-154-96) |
NDC Information of Clarifoam EF
| NDC Code | 16781-154-96 |
| Proprietary Name | Clarifoam EF |
| Package Description | 100 g in 1 CAN (16781-154-96) |
| Product NDC | 16781-154 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SULFUR,SULFACETAMIDE SODIUM |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Onset Dermatologics LLC |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 10; 5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
