Pulsatilla

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
6308371311
29.5 mL in 1 BOTTLE, DROPPER (63083-7131-1)

Annotations

UNII (FDA Substance ID)

24K790T39B

PULSATILLA MONTANA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "24K790T39B",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PULSATILLA MONTANA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "02df74e5-dcb0-4942-8c07-87faf18f145d": {
      "match": "brand_token",
      "title": "PULSATILLA 7131 (PULSATILLA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "63083-7131_336fa763-4c54-4dba-a649-023c0606e5ea",
  "productndc": "63083-7131",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PULSATILLA MONTANA WHOLE",
  "proprietary_name": "Pulsatilla",
  "active_ingred_unit": "[hp_X]/29.5mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulsatilla",
  "start_marketing_date": "19840815",
  "active_numerator_strength": "6"
}

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