NDC11 72189062135
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 |
|---|---|
| 72189-0621-35 | 72189-0621 |
| 72189-621-35 | 72189-621 |
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 |
|---|---|---|---|---|---|---|
| Lidothol Gel | LIDOTHOL GEL | Direct_Rx | 34f15ceb-87c1-526d-e063-6294a90a3789 | 2026-03-17 | Warnings, Adverse reactions | 72189-621-35 72189-621 72189062135 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.