NDC11 59316000210
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 |
|---|---|
| 59316-0002-10 | 59316-0002 |
| 59316-002-10 | 59316-002 |
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 Foot Pain Relief Set | MENTHOL | Reckitt Benckiser LLC | 4a885eef-0364-4655-bccc-7158c76cc5b2 | 2026-05-13 | Warnings | 59316-002-10 59316-002 59316000210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.