NDC11 69625094301
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 |
|---|---|
| 69625-0943-01 | 69625-0943 |
| 69625-0943-1 | 69625-0943 |
| 69625-943-01 | 69625-943 |
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 |
|---|---|---|---|---|---|---|
| La Roche Posay Laboratoire Dermatologique Anthelios Tinted Mineral Light Fluid Sunscreen Broad Spectrum SPF 40 Medium Deep | TITANIUM DIOXIDE AND ZINC OXIDE | Cosmetique Active Production | 0cb8f22d-2343-415e-9f16-1791567864a1 | 2023-12-16 | Warnings | 69625-943-01 69625-943 69625094301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.