Home NDC 63629-9259-1 Sodium Sulfacetamide and Sulfur
Product NDC 63629-9259
Requested package NDC 63629-9259-1
11-digit product format 636299259
Labeler code 63629
Product ID 63629-9259_404f3bc8-e28d-4045-bb52-05edd784e2f7
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 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Sodium Sulfacetamide and Sulfur
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFACETAMIDE SODIUM 100 mg/g SULFUR 50 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 999613 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63629-9259-1 Sodium Sulfacetamide and Sulfur 170 g in 1 BOTTLE, PLASTIC LIQUID 170 103
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63629-9259 SODIUM SULFACETAMIDE AND SULFUR (SULFACETAMIDE SODIUM, SULFUR) LIQUID [BRYANT RANCH PREPACK] 102 Current NDC, Legacy NDC, 1 package rows 20240510_aaa87a7b-1ff7-43df-b82b-66dee775d851.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63629-9259-1 63629925901 170 g in 1 BOTTLE, PLASTIC (63629-9259-1) 170 g 2021-11-15 0000-00-00 No No Current