Helleborus e pl. tota 12

UNIISPL

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

Identification

ManufacturerUriel Pharmacy Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4895151081
10 AMPULE in 1 BOX (48951-5108-1) / 1 mL in 1 AMPULE

Annotations

UNII (FDA Substance ID)

332Y7EES96

HELLEBORUS FOETIDUS ROOT

RxCUI 2047647

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "332Y7EES96",
    "rxcui": "2047647",
    "inchikey": null,
    "display_name": "HELLEBORUS FOETIDUS 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": "48951-5108_2c532194-0bac-f221-e063-6394a90a4ab9",
  "productndc": "48951-5108",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HELLEBORUS FOETIDUS ROOT",
  "proprietary_name": "Helleborus e pl. tota 12",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Helleborus e pl. tota 12",
  "start_marketing_date": "20090901",
  "active_numerator_strength": "12"
}

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