NDC11 85376020250
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 |
|---|---|
| 85376-0202-50 | 85376-0202 |
| 85376-202-50 | 85376-202 |
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 |
|---|---|---|---|---|---|---|
| Non-Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | HSC MIAMI, INC | 36d9a8f3-7760-57f3-e063-6394a90a1a1e | 2025-12-17 | 85376-202 | |
| Non-Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | HSC MIAMI, INC | 36d7a18b-5a12-84a9-e063-6394a90a7e38 | 2025-12-17 | 85376-202-50 85376-202 85376020250 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.