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United States · US · US:0220-2450_003a848f-c8d0-0cb1-e063-6294a90a6602
Helleborus niger
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBoiron
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110220245041200 [kp_C] in 1 TUBE (0220-2450-41)
Annotations
UNII (FDA Substance ID)
608DGJ6815
HELLEBORUS NIGER ROOT
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "608DGJ6815",
"rxcui": null,
"inchikey": null,
"display_name": "HELLEBORUS NIGER ROOT",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"150e57ad-3ed7-5cc9-e063-6394a90a25fe": {
"match": "brand_token",
"title": "HELLEBORUS COMP. A LIQUID [URIEL PHARMACY INC.]",
"spl_version": "3",
"published_date": "2025-11-24"
}
},
"productid": "0220-2450_003a848f-c8d0-0cb1-e063-6294a90a6602",
"productndc": "0220-2450",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "HELLEBORUS NIGER ROOT",
"proprietary_name": "Helleborus niger",
"active_ingred_unit": "[kp_C]/200[kp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "HELLEBORUS NIGER ROOT",
"start_marketing_date": "19830303",
"active_numerator_strength": "200"
}Access this data programmatically
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