NDC11 63742001300
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 |
|---|---|
| 63742-0013-0 | 63742-0013 |
| 63742-0013-00 | 63742-0013 |
| 63742-013-00 | 63742-013 |
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 |
|---|---|---|---|---|---|---|
| Lightning Pain Relief | MENTHOL | Clinical Resolution Laboratory, Inc. | 80af21f5-dba8-42b0-8a65-ac5a94d83ca8 | 2026-03-02 | Warnings | 63742-013-00 63742-013 63742001300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.