NDC11 87063021899
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 |
|---|---|
| 87063-0218-99 | 87063-0218 |
| 87063-218-99 | 87063-218 |
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 | LIDOCAINE HCL, MENTHOL | ASCLEMED USA INC. | 4e2fad18-13f1-4e61-86db-d72102928717 | 2026-05-28 | Warnings, Adverse reactions | 87063-218-99 87063-218 87063021899 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.