NDC11 69625020302
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 |
|---|---|
| 69625-0203-02 | 69625-0203 |
| 69625-0203-2 | 69625-0203 |
| 69625-203-02 | 69625-203 |
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 Deep | TITANIUM DIOXIDE AND ZINC OXIDE | Cosmetique Active Production | 8bdd63f7-2f67-4280-9484-d6c8e80ad9b9 | 2023-12-16 | Warnings | 69625-203-02 69625-203 69625020302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.