NDC11 72654001300
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 |
|---|---|
| 72654-0013-0 | 72654-0013 |
| 72654-0013-00 | 72654-0013 |
| 72654-013-00 | 72654-013 |
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 | Ebanel Laboratories, Inc | 36edbc3f-501c-c1ea-e063-6394a90af6af | 2025-06-06 | Warnings | 72654-013-00 72654-013 72654001300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.