NDC11 71399048406
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 |
|---|---|
| 71399-0484-06 | 71399-0484 |
| 71399-0484-6 | 71399-0484 |
| 71399-484-06 | 71399-484 |
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 |
|---|---|---|---|---|---|---|
| Sodium Sulfacetamide 9% - Sulfur 4.5% Wash | SULFACETAMIDE SODIUM, SULFUR | Akron Pharma Inc. | 29c84706-b96b-45e8-b84a-b130a2d1e9b5 | 2024-09-24 | Warnings, Adverse reactions | 71399-0484-6 71399-0484 71399048406 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.