NDC11 59088039100
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 |
|---|---|
| 59088-0391-0 | 59088-0391 |
| 59088-0391-00 | 59088-0391 |
| 59088-391-00 | 59088-391 |
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 |
|---|---|---|---|---|---|---|
| DermacinRx Clorhexacin | MUPIROCIN OINTMENT | PureTek Corporation | 3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f9 | 2024-12-13 | Warnings, Adverse reactions | 59088-391-00 59088-391 59088039100 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.