Pulsatilla

UNIISPL

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

Identification

ManufacturerSEVENE USA

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7647230301
80 PELLET in 1 CYLINDER (76472-3030-1)

Annotations

UNII (FDA Substance ID)

6J43Y8MXF0

PULSATILLA ALPINA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "6J43Y8MXF0",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PULSATILLA ALPINA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "SUBLINGUAL",
  "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": "76472-3030_2ddc5fae-8d3c-7121-e063-6294a90a6aad",
  "productndc": "76472-3030",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PULSATILLA ALPINA WHOLE",
  "proprietary_name": "Pulsatilla",
  "active_ingred_unit": "[kp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Pulsatilla",
  "start_marketing_date": "20111123",
  "active_numerator_strength": "200"
}

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