NDC11 84126022410
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 |
|---|---|
| 84126-0224-10 | 84126-0224 |
| 84126-224-10 | 84126-224 |
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 |
|---|---|---|---|---|---|---|
| Gillette Ultimate Protection Cool Wave | ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY | The Procter & Gamble Manufacturing Company | 4bac02ec-2692-5894-e063-6394a90a4bf9 | 2026-02-25 | Warnings | 84126-224-10 84126-224 84126022410 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.