Pulsatilla

UNIISPL

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

Identification

ManufacturerEnergique, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4491104981
30 mL in 1 BOTTLE, DROPPER (44911-0498-1)

Annotations

UNII (FDA Substance ID)

8E272251DI

PULSATILLA PRATENSIS WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "8E272251DI",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PULSATILLA PRATENSIS 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": "44911-0498_e648ebdd-a77d-43b2-ba31-e2dd2d80338c",
  "productndc": "44911-0498",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PULSATILLA PRATENSIS WHOLE",
  "proprietary_name": "Pulsatilla",
  "active_ingred_unit": "[hp_C]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulsatilla (Pratensis)",
  "start_marketing_date": "20190607",
  "active_numerator_strength": "200"
}

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