NDC11 58411067011
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 |
|---|---|
| 58411-0670-11 | 58411-0670 |
| 58411-670-11 | 58411-670 |
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 |
|---|---|---|---|---|---|---|
| SHISEIDO URBAN ENVIRONMENT Oil-Free SUNSCREEN SPF 42 | ENSULIZOLE, HOMOSALATE, OCTISALATE, AND ZINC OXIDE | SHISEIDO AMERICAS CORPORATION | 21bde283-a554-45c8-8733-2a8adeff41b1 | 2025-03-20 | Warnings | 58411-670-11 58411-670 58411067011 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.