NDC11 85394020315
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 |
|---|---|
| 85394-0203-15 | 85394-0203 |
| 85394-203-15 | 85394-203 |
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 |
|---|---|---|---|---|---|---|
| Tinted Mineral Matte CE Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | The Maui Medical Group, Inc | 34b72d14-b69b-e9dd-e063-6394a90a748e | 2025-12-11 | 85394-203-15 85394-203 85394020315 | |
| Tinted Mineral Matte CE Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | The Maui Medical Group, Inc | 34b60880-5fe1-b78f-e063-6294a90a748d | 2025-12-11 | 85394-203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.