NDC11 72578008601
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 |
|---|---|
| 72578-0086-01 | 72578-0086 |
| 72578-0086-1 | 72578-0086 |
| 72578-086-01 | 72578-086 |
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 |
|---|---|---|---|---|---|---|
| Desonide | DESONIDE | Viona Pharmaceuticals Inc | fdeb2a20-a612-4ae5-9178-222295271274 | 2026-01-12 | Adverse reactions | 72578-086-01 72578-086 72578008601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.