NDC11 83866176201
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 |
|---|---|
| 83866-1762-01 | 83866-1762 |
| 83866-1762-1 | 83866-1762 |
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 |
|---|---|---|---|---|---|---|
| Omnilux Mineral Facial Sunscreen | ZINC OXIDE | The Lotus Global Group, Inc, dba GlobalMed Technologies | 5710c84b-9d6b-da4d-e063-6394a90a0737 | 2026-07-20 | Warnings | 83866-1762-1 83866-1762 83866176201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.