NDC11 28595050108
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 28595-0501-08 | 28595-0501 |
| 28595-0501-8 | 28595-0501 |
| 28595-501-08 | 28595-501 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| sulfacetamide sodium and sulfur Sodium Sulfacetamide - Sulfur | SULFACETAMIDE SODIUM AND SULFUR | Allegis Pharmaceuticals, LLC | 1aa1025f-c568-34d3-e063-6394a90a37b8 | 2026-02-11 | Warnings, Adverse reactions | 28595-501-08 28595-501 28595050108 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.