NDC11 49967046001
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 |
|---|---|
| 49967-0460-01 | 49967-0460 |
| 49967-0460-1 | 49967-0460 |
| 49967-460-01 | 49967-460 |
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 HA Mineral Broad Spectrum SPF 30 Daily Moisturizing Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | L'Oreal USA Products Inc | 7bca5947-88a3-4cb3-a6f2-9fa389d344ef | 2024-01-01 | Warnings | 49967-460-01 49967-460 49967046001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.