Sodium Sulfacetamide 9% - Sulfur 4.5% Wash
NDC 71399-0484, SULFACETAMIDE SODIUM, SULFUR, liquid, from Akron Pharma Inc..
- Product NDC
- 71399-0484
- Status
- Listed
- Labeler
- Akron Pharma Inc.
- Dosage form
- LIQUID
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0484 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFACETAMIDE SODIUM90 mg/g
- SULFUR45 mg/g
Pharmacologic classes
Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71399-0484-6 | 71399048406 | 454 g in 1 BOTTLE, PLASTIC (71399-0484-6) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/29c84706-b96b-45e8-b84a-b130a2d1e9b5
Use it
Look up 71399-0484 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0484 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71399-0484. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.