NDC11 78691003500
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 |
|---|---|
| 78691-0035-0 | 78691-0035 |
| 78691-0035-00 | 78691-0035 |
| 78691-035-00 | 78691-035 |
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 |
|---|---|---|---|---|---|---|
| Biopure Antibacterial Hand Wipe Berry Strawberry | BENZALKONIUM CHLORIDE | Quest USA Corp | 47d6574c-0d4c-392e-e063-6394a90a590f | 2026-01-07 | Warnings | 78691-035-00 78691-035 78691003500 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.