Sodium Sulfacetamide and Sulfur

Product NDC
72162-1664
11-digit product format
721621664
Labeler code
72162
Product ID
72162-1664_392ccc80-3b7c-40e9-b7e2-ab6f8b170888
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SULFACETAMIDE SODIUM, SULFUR
Dosage form
LIQUID
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2021-11-15
Substance
SULFACETAMIDE SODIUM; SULFUR
Active strength
100; 50 mg/g; mg/g
Pharmacologic classes
Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4NRT660KJQSULFACETAMIDE SODIUM6209-17-2SULFACETAMIDE SODIUM
70FD1KFU70SULFUR7704-34-9SULFUR

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1664-272162166402277 g in 1 BOTTLE, PLASTIC (72162-1664-2) 277 g2024-01-30NoNoHistorical
72162-1664-472162166404340 g in 1 BOTTLE, PLASTIC (72162-1664-4) 340 g2024-01-30NoNoHistorical
72162-1664-772162166407340.2 g in 1 BOTTLE, PLASTIC (72162-1664-7) 340.2 g2024-01-30NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sodium Sulfacetamide 10% - Sulfur 5% CleanserBryant Ranch Prepack2024-12-24HUMAN PRESCRIPTION DRUG LABEL101