NDC11 59088025907
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 |
|---|---|
| 59088-0259-07 | 59088-0259 |
| 59088-0259-7 | 59088-0259 |
| 59088-259-07 | 59088-259 |
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 |
|---|---|---|---|---|---|---|
| Camphor 4% Plus Menthol 10% | CAMPHOR 4% PLUS MENTHOL 10% | PureTek Corporation | 3cab26e4-e377-f26a-e063-6394a90a17af | 2025-08-20 | Warnings | 59088-259-07 59088-259 59088025907 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.