Product NDC: | 42546-175 |
Proprietary Name: | SulfaCleanse 8/4 |
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): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42546-175 |
Labeler Name: | PruGen, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110501 |
Package NDC: | 42546-175-16 |
Package Description: | 1 BOTTLE, PUMP in 1 BOX (42546-175-16) > 473 mL in 1 BOTTLE, PUMP |
NDC Code | 42546-175-16 |
Proprietary Name | SulfaCleanse 8/4 |
Package Description | 1 BOTTLE, PUMP in 1 BOX (42546-175-16) > 473 mL in 1 BOTTLE, PUMP |
Product NDC | 42546-175 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium sulfacetamide and sulfur |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110501 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | PruGen, Inc. |
Substance Name | SULFACETAMIDE SODIUM; SULFUR |
Strength Number | 80; 40 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |