NDC11 51452003606
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 |
|---|---|
| 51452-0036-06 | 51452-0036 |
| 51452-0036-6 | 51452-0036 |
| 51452-036-06 | 51452-036 |
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 |
|---|---|---|---|---|---|---|
| Point Relief Cold Spot Pain Relieving | MENTHOL | Fabrication Enterprises | 391af69f-74aa-48cf-bc96-75e5c4e0e445 | 2023-11-05 | Warnings | 51452-036-06 51452-036 51452003606 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.