NDC11 85774020315
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 |
|---|---|
| 85774-0203-15 | 85774-0203 |
| 85774-203-15 | 85774-203 |
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 |
|---|---|---|---|---|---|---|
| PURE Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | LA JOLLA WELLNESS & AESTHETICS | 386bb911-9dbb-30fb-e063-6394a90a5e4d | 2025-12-15 | 85774-203 | |
| PURE Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | LA JOLLA WELLNESS & AESTHETICS | 386c0261-68f9-6f27-e063-6294a90a8209 | 2025-12-15 | 85774-203-15 85774-203 85774020315 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.