NDC11 10738005941
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 |
|---|---|
| 10738-0059-41 | 10738-0059 |
| 10738-059-41 | 10738-059 |
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 |
|---|---|---|---|---|---|---|
| TRIDERMA EVERYDAY BRUISE RELIEF | ARNICA MONTANA | Genuine Virgin Aloe Corporation | 5100f2d0-cfa2-4136-bda4-860de81707c8 | 2026-01-28 | Warnings | 10738-059-41 10738-059 10738005941 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.