NDC11 85260028202
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 |
|---|---|
| 85260-0282-02 | 85260-0282 |
| 85260-0282-2 | 85260-0282 |
| 85260-282-02 | 85260-282 |
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 |
|---|---|---|---|---|---|---|
| Sonni SunDay Serum | ZINC OXIDE | Sonni | 419d4ada-fe9b-b774-e063-6394a90a3d09 | 2025-10-20 | Warnings | 85260-282-02 85260-282 85260028202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.