NDC11 59316010320
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 |
|---|---|
| 59316-0103-20 | 59316-0103 |
| 59316-103-20 | 59316-103 |
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 Colorless | MENTHOL | Reckitt Benckiser LLC | 939dbbc3-71ec-4990-840e-7c9b8d430562 | 2026-05-13 | Warnings | 59316-103-20 59316-103 59316010320 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.