NDC11 65923083130
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 |
|---|---|
| 65923-0831-30 | 65923-0831 |
| 65923-831-30 | 65923-831 |
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 |
|---|---|---|---|---|---|---|
| Coralite Antibacterial Moist | BENZALKONIUM CHLORIDE | United Exchange Corp. | 6245a83f-5c81-4ae6-bc6e-adfc46c37003 | 2025-10-31 | Warnings | 65923-831-30 65923-831 65923083130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.