NDC11 66096070825
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 |
|---|---|
| 66096-0708-25 | 66096-0708 |
| 66096-708-25 | 66096-708 |
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 |
|---|---|---|---|---|---|---|
| Kids Cough Relief Syrup | ANTIMONIUM SULPHURATUM AUREUM, ANTIMONIUM TARTARICUM, BRYONIA ALBA, DROSERA ROTUNDIFOLIA, IPECACUANHA, KALI MURIATICUM, RUMEX CRISPUS, SENEGA OFFICINALIS, SPONGIA TOSTA. | OHM PHARMA INC. | b09a9fbc-15ad-4c60-bce8-e1097d241f2c | 2021-12-29 | Warnings | 66096-708-25 66096-708 66096070825 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.