SULFACETAMIDE SODIUM, SULFUR
Sodium Sulfacetamide 10% & Sulfur 5% Cleanser (in a urea vehicle)
Approved
Approval ID
f433db67-d8a6-320e-e053-2995a90aab52
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 6, 2023
Manufacturers
FDA
Bantry Pharma, LLC
DUNS: 117871480
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
SULFACETAMIDE SODIUM, SULFUR
PRODUCT DETAILS
NDC Product Code81542-202
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateSeptember 6, 2023
Generic NameSULFACETAMIDE SODIUM, SULFUR
INGREDIENTS (3)
UREAInactive
Quantity: 100 mg in 1 mL
Code: 8W8T17847W
Classification: IACT
SULFURActive
Quantity: 50 mg in 1 mL
Code: 70FD1KFU70
Classification: ACTIB
SULFACETAMIDE SODIUMActive
Quantity: 100 mg in 1 mL
Code: 4NRT660KJQ
Classification: ACTIB