Belladonna

UNIISPL

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

Identification

ManufacturerProfessional Complementary Health Formulas

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6308371061
29.5 mL in 1 BOTTLE, DROPPER (63083-7106-1)

Annotations

UNII (FDA Substance ID)

11B89M58UN

AMARYLLIS BELLADONNA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "11B89M58UN",
    "rxcui": null,
    "inchikey": null,
    "display_name": "AMARYLLIS BELLADONNA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "84771ac5-acf1-e0ec-e053-2a91aa0a1b36": {
      "match": "brand_token",
      "title": "BELLADONNA (ATROPA BELLADONNA\t) PELLET [BOIRON]",
      "spl_version": "5",
      "published_date": "2026-04-28"
    }
  },
  "productid": "63083-7106_3be49031-d519-4f43-a125-5be8f767e71c",
  "productndc": "63083-7106",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMARYLLIS BELLADONNA WHOLE",
  "proprietary_name": "Belladonna",
  "active_ingred_unit": "[hp_X]/29.5mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Belladonna",
  "start_marketing_date": "19840815",
  "active_numerator_strength": "6"
}

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