NDC11 61096103501
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 |
|---|---|
| 61096-1035-01 | 61096-1035 |
| 61096-1035-1 | 61096-1035 |
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 |
|---|---|---|---|---|---|---|
| Rejuvenation Plus | ARALIA QUIN, ARNICA, AVENA, BARYTA CARB, CARDUUS MAR, DNA, HEPAR SUIS, MEDULLA OSSIS SUIS, PANCREAS SUIS, PHOSPHORICUM AC, PITUITARUM POSTERIUM, THUJA OCC | Eight and Company L.L.C | bdcdee99-c0e8-4b8c-a0cc-009ecb1ddaae | 2025-12-18 | Warnings | 61096-1035-1 61096-1035 61096103501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.