NDC11 71897022486
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 |
|---|---|
| 71897-0224-86 | 71897-0224 |
| 71897-224-86 | 71897-224 |
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 |
|---|---|---|---|---|---|---|
| Foaming Hand | BENZALKONIUM CHLORIDE | Veritiv Operating Company | 3b4dbfd0-f275-3502-e063-6294a90a8486 | 2026-02-16 | Warnings, Adverse reactions | 71897-224-86 71897-224 71897022486 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.