Product NDC: | 54295-301 |
Proprietary Name: | Sodium Sulfacetamide 9 Sulfur 4.5 Wash |
Non Proprietary Name: | Sulfacetamide Sodium and Sulfur |
Active Ingredient(s): | 9; 4.5 mg/g; mg/g & nbsp; Sulfacetamide Sodium and Sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54295-301 |
Labeler Name: | Trinity Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20121210 |
Package NDC: | 54295-301-21 |
Package Description: | 1 BOTTLE in 1 CARTON (54295-301-21) > 454 g in 1 BOTTLE |
NDC Code | 54295-301-21 |
Proprietary Name | Sodium Sulfacetamide 9 Sulfur 4.5 Wash |
Package Description | 1 BOTTLE in 1 CARTON (54295-301-21) > 454 g in 1 BOTTLE |
Product NDC | 54295-301 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sulfacetamide Sodium and Sulfur |
Dosage Form Name | RINSE |
Route Name | TOPICAL |
Start Marketing Date | 20121210 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Trinity Pharmaceuticals, LLC |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 9; 4.5 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |