Sodium Sulfacetamide 8% and Sulfur 4%
Sodium Sulfacetamide 8% - Sulfur 4% Topical SuspensionIn a vehicle containing Green Tea and Aloe
Approved
Approval ID
bfbe625c-5679-4363-913a-2ab03198f4f0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 26, 2023
Manufacturers
FDA
Akron Pharma Inc.
DUNS: 067878881
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 Code71399-0487
Product Classification
G
Generic Name
SULFACETAMIDE SODIUM, SULFUR
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 12, 2023
FDA Product Classification
INGREDIENTS (17)
SULFACETAMIDE SODIUMActive
Quantity: 80 mg in 1 mL
Code: 4NRT660KJQ
Classification: ACTIB
SULFURActive
Quantity: 40 mg in 1 mL
Code: 70FD1KFU70
Classification: ACTIB
BENZYL ALCOHOLInactive
Code: LKG8494WBH
Classification: IACT
ALOE VERA LEAFInactive
Code: ZY81Z83H0X
Classification: IACT
CETYL ALCOHOLInactive
Code: 936JST6JCN
Classification: IACT
BUTYLATED HYDROXYTOLUENEInactive
Code: 1P9D0Z171K
Classification: IACT
GLYCERYL MONOSTEARATEInactive
Code: 230OU9XXE4
Classification: IACT
GREEN TEA LEAFInactive
Code: W2ZU1RY8B0
Classification: IACT
MAGNESIUM ALUMINUM SILICATEInactive
Code: 6M3P64V0NC
Classification: IACT
PEG-40 STEARATEInactive
Code: ECU18C66Q7
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM THIOSULFATEInactive
Code: HX1032V43M
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT
PHENOXYETHANOLInactive
Code: HIE492ZZ3T
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
STEARYL ALCOHOLInactive
Code: 2KR89I4H1Y
Classification: IACT