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United States Β· US Β· US:0220-1953_0a0cca60-17d2-b93d-e063-6394a90a0731

Eupatorium perfoliatum

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBoiron
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    0220195341
    12 [hp_C] in 1 TUBE (0220-1953-41)

Annotations

UNII (FDA Substance ID)
1W0775VX6E
EUPATORIUM PERFOLIATUM FLOWERING TOP
RxCUI 1309783
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "1W0775VX6E",
    "rxcui": "1309783",
    "inchikey": null,
    "display_name": "EUPATORIUM PERFOLIATUM FLOWERING TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "8689017a-c21a-4b0b-9c13-9c5cde4a9148": {
      "match": "brand_token",
      "title": "EUPATORIUM PERFOLIATUM 7118 (EUPATORIUM PERFOLIATUM) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "0220-1953_0a0cca60-17d2-b93d-e063-6394a90a0731",
  "productndc": "0220-1953",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "EUPATORIUM PERFOLIATUM FLOWERING TOP",
  "proprietary_name": "Eupatorium perfoliatum",
  "active_ingred_unit": "[hp_C]/12[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "EUPATORIUM PERFOLIATUM FLOWERING TOP",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "12"
}

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