NDC11 65923021401
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 |
|---|---|
| 65923-0214-01 | 65923-0214 |
| 65923-0214-1 | 65923-0214 |
| 65923-214-01 | 65923-214 |
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 |
|---|---|---|---|---|---|---|
| Coralite Cold and Hot | MENTHOL | United Exchange Corp. | 064a6149-a0e2-8a73-e063-6394a90a7953 | 2025-10-22 | Warnings | 65923-214-01 65923-214 65923021401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.