NDC11 49967089902
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 |
|---|---|
| 49967-0899-02 | 49967-0899 |
| 49967-0899-2 | 49967-0899 |
| 49967-899-02 | 49967-899 |
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 50 Tinted Mineral Sunscreen | TITANIUM DIOXIDE | L'Oreal USA Products Inc | 6d3c5fc5-c818-46c4-8db3-cffcdcd56e06 | 2023-12-31 | Warnings | 49967-899-02 49967-899 49967089902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.