NDC11 52257145001
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 |
|---|---|
| 52257-1450-01 | 52257-1450 |
| 52257-1450-1 | 52257-1450 |
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 |
|---|---|---|---|---|---|---|
| Atomy Sunscreen White Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | b8bc0021-bb4d-45f2-a570-3f2e61edf21d | 2024-02-16 | Warnings | 52257-1450-1 52257-1450 52257145001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.