NDC11 77677001320
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 |
|---|---|
| 77677-0013-20 | 77677-0013 |
| 77677-013-20 | 77677-013 |
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 |
|---|---|---|---|---|---|---|
| Hand Wipes | BENZALKONIUM CHLORIDE | Advanced Ultrasound Solutions Inc. | 2c2abaa8-c152-470b-a4d9-5056815a1987 | 2025-12-05 | Warnings | 77677-013-20 77677-013 77677001320 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.