NDC11 87572021930
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 |
|---|---|
| 87572-0219-30 | 87572-0219 |
| 87572-219-30 | 87572-219 |
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 Stick Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | UNDRBUDR, LLC | 4f83dd76-a8d8-916e-e063-6294a90ab6ed | 2026-04-15 | Warnings | 87572-219-30 87572-219 87572021930 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.