NDC11 61096100301
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 |
|---|---|
| 61096-1003-01 | 61096-1003 |
| 61096-1003-1 | 61096-1003 |
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 |
|---|---|---|---|---|---|---|
| AllergEase | ALLIUM CEPA, APIS MELLIFICA, ARALIA RAC, ARUNDO, BAPTISIA, ECHINACEA, EUPHRASIA, GELSEMIUM, HISTAMINUM, LYCOPODIUM, RHUS TOX, SABADILLA, SANGUINARIA, URTICA UR. | Eight and Company L.L.C | ec4fae96-ffe3-489c-9ed2-4aaec114c493 | 2025-12-18 | Warnings | 61096-1003-1 61096-1003 61096100301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.