NDC11 72562016725
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 |
|---|---|
| 72562-0167-25 | 72562-0167 |
| 72562-167-25 | 72562-167 |
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 |
|---|---|---|---|---|---|---|
| Pain Relief Liquid Roller | CAMPHOR 3.5%, MENTHOL 3.5% | Tommie Copper, Inc. | c9f0447e-de43-16a5-e053-2995a90a05c1 | 2024-12-15 | Warnings | 72562-167-25 72562-167 72562016725 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.