NDC11 71825015172
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 |
|---|---|
| 71825-0151-72 | 71825-0151 |
| 71825-151-72 | 71825-151 |
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 |
|---|---|---|---|---|---|---|
| Cremo Company | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (ANHYDROUS) | Cremo Company, LLC | 297e9178-5f4e-c7cc-e063-6294a90a2c29 | 2024-12-17 | Warnings | 71825-151-72 71825-151 71825015172 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.