Helleborus niger

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerWashington Homeopathic Products

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7191981801
350 PELLET in 1 VIAL, GLASS (71919-818-01)

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": "71919-818_2cc87829-1807-784b-e063-6394a90ae295",
  "productndc": "71919-818",
  "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": "20231107",
  "active_numerator_strength": "200"
}

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