NDC11 59088021505
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 |
|---|---|
| 59088-0215-05 | 59088-0215 |
| 59088-0215-5 | 59088-0215 |
| 59088-215-05 | 59088-215 |
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 |
|---|---|---|---|---|---|---|
| Mencylate Pain Relieving | MENTHOL, METHYL SALICYLATE | PureTek Corporation | f824de86-9492-2e6b-e053-6294a90a6f2a | 2024-10-01 | Warnings | 59088-215-05 59088-215 59088021505 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.