SODIUM SULFACETAMIDE, SULFUR
- Product NDC
- 87026-202
- 11-digit product format
- 870260202
- Labeler code
- 87026
- Product ID
- 87026-202_46064e69-cc1a-8cee-e063-6394a90a8d32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Sulfacetamide 10%, Sulfur 5%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Aspen Medical LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-01-01
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SODIUM SULFACETAMIDE, SULFUR
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFACETAMIDE SODIUM | 100 mg/g |
| SULFUR | 50 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4NRT660KJQ, 70FD1KFU70 |
| Rxcui | 999613 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87026-202-06 | SODIUM SULFACETAMIDE, SULFUR | 170 g in 1 BOTTLE | LIQUID | 170 | | 1 |
| 87026-202-12 | SODIUM SULFACETAMIDE, SULFUR | 340 g in 1 BOTTLE | LIQUID | 340 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87026-202-06 | 87026020206 | 170 g in 1 BOTTLE (87026-202-06) | 170 g | 2026-01-01 | No | No | Historical |
| 87026-202-12 | 87026020212 | 340 g in 1 BOTTLE (87026-202-12) | 340 g | 2026-01-01 | No | No | Historical |