NDC11 51326082903
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 |
|---|---|
| 51326-0829-03 | 51326-0829 |
| 51326-0829-3 | 51326-0829 |
| 51326-829-03 | 51326-829 |
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 |
|---|---|---|---|---|---|---|
| Antioxidant Sunscreen SPF 40 | OCTINOXATE AND ZINC OXIDE | Topiderm, Inc. | 2686378c-8827-47fb-b3ed-07438bd4e9e2 | 2019-11-13 | Warnings | 51326-829-03 51326-829 51326082903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.