Sodium Sulfacetamide and Sulfer Emulsion
- Product NDC
- 73352-750
- 11-digit product format
- 733520750
- Labeler code
- 73352
- Product ID
- 73352-750_41396a22-cc34-94f2-e063-6294a90afb65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Sulfacetamide and Sulfer
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- Trifluent Pharma
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-10-04
- Substance
- SULFACETAMIDE SODIUM; SULFUR
- Active strength
- 100; 10 mg/mL; mg/mL
- 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 and Sulfer Emulsion
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFACETAMIDE SODIUM | 100 mg/mL |
| SULFUR | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4NRT660KJQ, 70FD1KFU70 |
| Rxcui | 999604 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73352-750-01 | Sodium Sulfacetamide and Sulfer Emulsion | 177 mL in 1 BOTTLE | EMULSION | 177 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73352-750-01 | 73352075001 | 177 mL in 1 BOTTLE (73352-750-01) | 177 ml | 2025-10-04 | No | No | Historical |