ACONITE

UNII

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
4491102091
30 mL in 1 BOTTLE, DROPPER (44911-0209-1)

Annotations

UNII (FDA Substance ID)

U0NQ8555JD

ACONITUM NAPELLUS WHOLE

RxCUI 1310220

Raw payload (JSON)

{
  "unii": {
    "unii": "U0NQ8555JD",
    "rxcui": "1310220",
    "inchikey": null,
    "display_name": "ACONITUM NAPELLUS WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "44911-0209_04259ae1-7e7d-4018-9866-9b0f378b2cfc",
  "productndc": "44911-0209",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACONITUM NAPELLUS WHOLE",
  "proprietary_name": "ACONITE",
  "active_ingred_unit": "[hp_C]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aconitum napellus",
  "start_marketing_date": "20150715",
  "active_numerator_strength": "200"
}

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