NDC11 85768020350
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 |
|---|---|
| 85768-0203-50 | 85768-0203 |
| 85768-203-50 | 85768-203 |
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 |
|---|---|---|---|---|---|---|
| Original Tint | TITANIUM DIOXIDE, ZINC OXIDE | L.S. MOORE LLC | 37f1e019-32c4-b733-e063-6394a90aca28 | 2025-12-09 | 85768-203-50 85768-203 85768020350 | |
| Original Tint | TITANIUM DIOXIDE, ZINC OXIDE | L.S. MOORE LLC | 37f2e363-e85f-f601-e063-6294a90ab120 | 2025-12-09 | 85768-203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.