SODIUM SULFACETAMIDE, SULFUR
- Product NDC
- 52187-530
- 11-digit product format
- 521870530
- Labeler code
- 52187
- Product ID
- 52187-530_b7123c28-8647-1526-e053-2a95a90a6ec3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium sulfacetamide, sulfur
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- KMM Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-01-30
- Substance
- SULFACETAMIDE SODIUM; SULFUR
- Active strength
- 90; 40 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, SULFUR
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFACETAMIDE SODIUM | 90 mg/mL |
| SULFUR | 40 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4NRT660KJQ, 70FD1KFU70 |
| Rxcui | 1001714 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52187-530-16 | SODIUM SULFACETAMIDE, SULFUR | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52187-530 | SODIUM SULFACETAMIDE, SULFUR LIQUID [KMM PHARMACEUTICALS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20201224_809f15db-a06a-649f-e053-2a91aa0ae9b0.zip |
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 |
|---|
| 52187-530-16 | 52187053016 | 473 mL in 1 BOTTLE, PLASTIC (52187-530-16) | 473 ml | 2019-01-30 | 0000-00-00 | No | No | Current |