NDC11 59088030707
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 |
|---|---|
| 59088-0307-07 | 59088-0307 |
| 59088-0307-7 | 59088-0307 |
| 59088-307-07 | 59088-307 |
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 |
|---|---|---|---|---|---|---|
| Lidotral 3.88% Roll on | LIDOCAINE HCI | PureTek Corporation | db1085fe-0a1f-c4cc-e053-2a95a90aa838 | 2024-02-28 | Warnings, Adverse reactions | 59088-307-07 59088-307 59088030707 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.