NDC11 71726000402
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 |
|---|---|
| 71726-0004-02 | 71726-0004 |
| 71726-0004-2 | 71726-0004 |
| 71726-004-02 | 71726-004 |
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 |
|---|---|---|---|---|---|---|
| FREEZE IT Menthol | MENTHOL | LiquidCapsule Manufacturing LLC | de8d8007-5718-4fb4-a8c6-4650d2ca9c8f | 2025-06-05 | Warnings | 71726-004-02 71726-004 71726000402 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.