NDC11 66096075402
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 |
|---|---|
| 66096-0754-02 | 66096-0754 |
| 66096-0754-2 | 66096-0754 |
| 66096-754-02 | 66096-754 |
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 |
|---|---|---|---|---|---|---|
| OHM-DREN LFT | APIS MELLIFICA, ARANEA DIADEMA, BERBERIS VULGARIS, EQUISETUM HYEMALE, GALIUM APARINE, JUGLANS REGIA, MANGANUM PHOSPHORICUM, NICOTINAMIDUM, NITRICUM ACIDUM, SARSAPARILLA, THUJA OCCIDENTALIS, URTICA URENS | OHM PHARMA INC. | 31f4eaab-fbd6-4924-b956-c0ff2934fbf0 | 2021-01-11 | Warnings | 66096-754-02 66096-754 66096075402 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.