NDC11 85558020250
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 |
|---|---|
| 85558-0202-50 | 85558-0202 |
| 85558-202-50 | 85558-202 |
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 |
|---|---|---|---|---|---|---|
| Mineral Sunscreen Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | LOTUS SKINCARE AND MAKE-UP STUDIO | 36b000e3-2516-932c-e063-6294a90a0e41 | 2025-12-17 | 85558-202-50 85558-202 85558020250 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.