Sodium Sulfacetamide and Sulfur
- Product NDC
- 71335-2940
- 11-digit product format
- 713352940
- Labeler code
- 71335
- Product ID
- 71335-2940_42535bb6-59d5-38d1-e063-6294a90a7754
- 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 UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4NRT660KJQ | SULFACETAMIDE SODIUM | 6209-17-2 | SULFACETAMIDE SODIUM |
| 70FD1KFU70 | SULFUR | 7704-34-9 | SULFUR |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2940-1 | 71335294001 | 227 g in 1 BOTTLE, PLASTIC (71335-2940-1) | 227 g | 2025-10-29 | No | No | Historical |