SULFACETAMIDE SODIUM, SULFUR
(sodium sulfacetamide 10%, sulfur 5%)
Approved
Approval ID
0e128306-1357-daad-e063-6294a90a760a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 23, 2024
Manufacturers
FDA
Cintex Services, LLC
DUNS: 078304114
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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code24470-933
Product Classification
G
Generic Name
SULFACETAMIDE SODIUM, SULFUR
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 23, 2024
FDA Product Classification
INGREDIENTS (2)
SULFURActive
Quantity: 50 mg in 1 g
Code: 70FD1KFU70
Classification: ACTIB
SULFACETAMIDE SODIUMActive
Quantity: 100 mg in 1 g
Code: 4NRT660KJQ
Classification: ACTIB