NDC11 61096203001
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 |
|---|---|
| 61096-2030-01 | 61096-2030 |
| 61096-2030-1 | 61096-2030 |
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 |
|---|---|---|---|---|---|---|
| Party Relief | ARSENICUM ALB, AVENA, BRYONIA, CAPSICUM, CARBO AN, CARDUUS MAR, CHELIDONIUM MAJ, HEPAR SUIS, KALI IOD, LAPIS, RADIUM BROM, TARAXACUM, THUJA OCC | Eight and Company L.L.C | efadeae2-1ed9-4e80-9909-908bde98965b | 2025-12-18 | Warnings | 61096-2030-1 61096-2030 61096203001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.