Sodium Sulfacetamide

Product NDC
72162-1665
11-digit product format
721621665
Labeler code
72162
Product ID
72162-1665_233623bf-3ee7-437d-a8e6-1a71bc16f299
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Sulfacetamide
Dosage form
LIQUID
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2022-01-15
Substance
SULFACETAMIDE SODIUM
Active strength
100 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

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1665-272162166502355 g in 1 BOTTLE (72162-1665-2) 355 g2024-12-24NoNoHistorical
72162-1665-472162166504480 g in 1 BOTTLE (72162-1665-4) 480 g2024-12-24NoNoHistorical
72162-1665-772162166507177 g in 1 BOTTLE (72162-1665-7) 177 g2024-12-24NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sodium Sulfacetamide 10%Bryant Ranch Prepack2024-12-24HUMAN PRESCRIPTION DRUG LABEL100