| Product NDC: | 42192-133 |
| Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Non Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Active Ingredient(s): | 80; 40 mg/mL; mg/mL & nbsp; Sodium Sulfacetamide and Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42192-133 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110727 |
| Package NDC: | 42192-133-16 |
| Package Description: | 473 mL in 1 BOTTLE (42192-133-16) |
| NDC Code | 42192-133-16 |
| Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Package Description | 473 mL in 1 BOTTLE (42192-133-16) |
| Product NDC | 42192-133 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 80; 40 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |