NDC11 80823069303
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 |
|---|---|
| 80823-0693-03 | 80823-0693 |
| 80823-0693-3 | 80823-0693 |
| 80823-693-03 | 80823-693 |
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 Sanitizer | HAND SANITIZER | Kandel & Son | bd9a7ce4-1b61-742f-e053-2995a90aa0f0 | 2024-12-08 | Warnings | 80823-693-03 80823-693 80823069303 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.