NDC11 77617000903
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 |
|---|---|
| 77617-0009-03 | 77617-0009 |
| 77617-0009-3 | 77617-0009 |
| 77617-009-03 | 77617-009 |
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 |
|---|---|---|---|---|---|---|
| Fresh Hands | BENZALKONIUM CHLORIDE | Maintex | e174083a-8820-4fa7-8cc2-0a2c86f27cd6 | 2025-12-22 | Warnings | 77617-009-03 77617-009 77617000903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.