NDC11 85374022030
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 |
|---|---|
| 85374-0220-30 | 85374-0220 |
| 85374-220-30 | 85374-220 |
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 |
|---|---|---|---|---|---|---|
| Tinted Mineral Sunscreen Stick | TITANIUM DIOXIDE, ZINC OXIDE | BABYFACE LLC | 36d80422-943f-3aba-e063-6294a90afb59 | 2025-06-05 | 85374-220-30 85374-220 85374022030 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.