NDC11 59088080200
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 |
|---|---|
| 59088-0802-0 | 59088-0802 |
| 59088-0802-00 | 59088-0802 |
| 59088-802-00 | 59088-802 |
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 |
|---|---|---|---|---|---|---|
| Diclogen | DICLOFENAC SODIUM, CAMPHOR AND MENTHOL | PureTek Corporation | 1e2bb4e5-bb65-48a0-e063-6294a90a54d1 | 2025-12-18 | Boxed warning, Warnings, Adverse reactions | 59088-802-00 59088-802 59088080200 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.