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United States · US · US:0220-2448_f527d8ba-5533-38ba-e053-2995a90a321c
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
- ndc11022024484180 PELLET in 1 TUBE (0220-2448-41)
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": "0220-2448_f527d8ba-5533-38ba-e053-2995a90a321c",
"productndc": "0220-2448",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "HELLEBORUS NIGER ROOT",
"proprietary_name": "Helleborus niger",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "HELLEBORUS NIGER ROOT",
"start_marketing_date": "19830303",
"active_numerator_strength": "6"
}Access this data programmatically
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