NDC11 59316012110
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 |
|---|---|
| 59316-0121-10 | 59316-0121 |
| 59316-121-10 | 59316-121 |
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 |
|---|---|---|---|---|---|---|
| Biofreeze Overnight Gel | MENTHOL | Reckitt Benckiser LLC | f5c8c08b-c7c0-f84d-e053-2a95a90add15 | 2026-05-15 | Warnings | 59316-121-10 59316-121 59316012110 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.