NDC11 85394022030
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 |
|---|---|
| 85394-0220-30 | 85394-0220 |
| 85394-220-30 | 85394-220 |
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 |
|---|---|---|---|---|---|---|
| Sheer Tinted Sunscreen Stick | TITANIUM DIOXIDE, ZINC OXIDE | The Maui Medical Group, Inc | 34b6e8d0-6235-dac2-e063-6394a90afefd | 2025-12-11 | 85394-220-30 85394-220 85394022030 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.