NDC11 58411095050
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 |
|---|---|
| 58411-0950-50 | 58411-0950 |
| 58411-950-50 | 58411-950 |
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 |
|---|---|---|---|---|---|---|
| VITAL PERFECTION UPLIFTING AND FIRMING ADVANCED DAY | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE | Shiseido Americas Corporation | 7b2d15c1-b9e1-4347-b138-9883f78822b3 | 2026-03-24 | Warnings | 58411-950-50 58411-950 58411095050 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.