NDC11 73240090501
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 |
|---|---|
| 73240-0905-01 | 73240-0905 |
| 73240-0905-1 | 73240-0905 |
| 73240-905-01 | 73240-905 |
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 |
|---|---|---|---|---|---|---|
| Mineral Ice Methol Pain Relief | MENTHOL 10.5 % | Sunflora Inc | 6ddd9e97-f717-4d5a-9658-26449a3cc831 | 2026-07-02 | Warnings | 73240-905-01 73240-905 73240090501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.