NDC11 58411048111
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 |
|---|---|
| 58411-0481-11 | 58411-0481 |
| 58411-481-11 | 58411-481 |
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 ULTIMATE SUN PROTECTOR | OCTISALATE, HOMOSALATE, OCTOCRYLENE, AND AVOBENZONE | SHISEIDO AMERICAS CORPORATION | 7a98171f-bf21-40d4-bc78-883aa0b0c438 | 2025-03-20 | Warnings | 58411-481-11 58411-481 58411048111 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.