NDC11 58411095210
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 |
|---|---|
| 58411-0952-10 | 58411-0952 |
| 58411-952-10 | 58411-952 |
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 | ENSULIZOLE, HOMOSALATE, OCTISALATE, ZINC OXIDE | Shiseido Americas Corporation | 8db9f5e0-a8d6-4872-b4c6-cb92c43d25c2 | 2025-12-16 | Warnings | 58411-952-10 58411-952 58411095210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.