NDC11 69469001301
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 |
|---|---|
| 69469-0013-01 | 69469-0013 |
| 69469-0013-1 | 69469-0013 |
| 69469-013-01 | 69469-013 |
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 |
|---|---|---|---|---|---|---|
| Mercurochrome | BENZALKONIUM CHLORIDE | Vitamex USA, Corp | 21652b11-715d-0c54-e063-6294a90a8855 | 2026-08-26 | Warnings | 69469-013-01 69469-013 69469001301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.