Product NDC: | 49808-154 |
Proprietary Name: | Sodium Sulfacetamide and Sulfur |
Non Proprietary Name: | SULFACETAMIDE SODIUM |
Active Ingredient(s): | 10; 5 g/100g; g/100g & nbsp; SULFACETAMIDE SODIUM |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49808-154 |
Labeler Name: | Metacon Labs |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100225 |
Package NDC: | 49808-154-60 |
Package Description: | 1 CAN in 1 BOX (49808-154-60) > 60 g in 1 CAN |
NDC Code | 49808-154-60 |
Proprietary Name | Sodium Sulfacetamide and Sulfur |
Package Description | 1 CAN in 1 BOX (49808-154-60) > 60 g in 1 CAN |
Product NDC | 49808-154 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SULFACETAMIDE SODIUM |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20100225 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Metacon Labs |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 10; 5 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |