NDC11 00472080302
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 |
|---|---|
| 00472-0803-02 | 00472-0803 |
| 00472-0803-2 | 00472-0803 |
| 00472-803-02 | 00472-803 |
| 0472-0803-02 | 0472-0803 |
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 | Actavis Pharma, Inc. | ff5d4cd8-ab4d-4a9e-b84b-445c81eeea99 | 2025-09-08 | Adverse reactions | 0472-0803-02 0472-0803 00472080302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.