NDC11 72226030500
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 |
|---|---|
| 72226-0305-0 | 72226-0305 |
| 72226-0305-00 | 72226-0305 |
| 72226-305-00 | 72226-305 |
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 |
|---|---|---|---|---|---|---|
| GOLD ICE Pain Relief | MENTHOL | Eden's Answers, Inc. | a1356c39-42b9-4bd8-a873-bcd40717058b | 2023-11-11 | Warnings | 72226-305-00 72226-305 72226030500 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.