United States · FDA National Drug Code directory
Sodium Sulfacetamide and Sulfur
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69367-245_b4e89e57-397a-4578-bc59-709cb46db033
- Product NDC
- 69367-245
- Form
- SUSPENSION
- Composition / generic term
- Sodium Sulfacetamide and Sulfur
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20210618
- Source listing expiry
- 20261231
Source-listed ingredients
- SULFACETAMIDE SODIUM — 80 mg/mL
- SULFUR — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (69367-245-16) · 69367-245-16
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →