NDC11 82404010111
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 |
|---|---|
| 82404-0101-11 | 82404-0101 |
| 82404-101-11 | 82404-101 |
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 |
|---|---|---|---|---|---|---|
| LUXURY SUN RITUAL PORE SMOOTHING SPF 30 SUNSCREEN | ZINC OXIDE | JANE STREET LLC | dbdd3e6a-f09d-90cf-e053-2a95a90a98a0 | 2026-01-07 | Warnings | 82404-101-11 82404-101 82404010111 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.