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) |
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 NDC: | 16781-154-06 |
Package Description: | 5 g in 1 CAN (16781-154-06) |
NDC Code | 16781-154-06 |
Proprietary Name | Clarifoam EF |
Package Description | 5 g in 1 CAN (16781-154-06) |
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] |