Home NDC 69367-244 SODIUM SULFACETAMIDE, SULFUR
Product NDC 69367-244
11-digit product format 693670244
Labeler code 69367
Product ID 69367-244_4fe0b59c-b850-44db-9670-a7499c724fea
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name sulfacetamide sodium and sulfur
Dosage form LIQUID
Route TOPICAL
Labeler Westminster Pharmaceuticals, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-05-05
Substance SULFACETAMIDE SODIUM; SULFUR
Active strength 98; 48 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 Additional Listing Data#
Finished product Yes
Brand name base SODIUM SULFACETAMIDE, SULFUR
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFACETAMIDE SODIUM 98 mg/g SULFUR 48 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4NRT660KJQ Internal UNII lookup 70FD1KFU70 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1494169 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69367-244-10 SODIUM SULFACETAMIDE, SULFUR 285 g in 1 BOTTLE LIQUID 285 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69367-244 SODIUM SULFACETAMIDE, SULFUR (SULFACETAMIDE SODIUM AND SULFUR) LIQUID [WESTMINSTER PHARMACEUTICALS, LLC] 8 Current NDC, Legacy NDC, 1 package rows 20250430_4478ac49-8984-42db-9b9e-bea6346a6955.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69367-244-10 69367024410 285 g in 1 BOTTLE (69367-244-10) 285 g 2020-05-05 0000-00-00 No No Current