Eucalyptus globulus

UNIISPL

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

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220193741
200 [kp_C] in 1 TUBE (0220-1937-41)

Annotations

UNII (FDA Substance ID)

S546YLW6E6

EUCALYPTUS GLOBULUS LEAF

RxCUI 1305545

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "S546YLW6E6",
    "rxcui": "1305545",
    "inchikey": null,
    "display_name": "EUCALYPTUS GLOBULUS LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "068ed8c0-1fff-42dd-a217-684201c16023": {
      "match": "brand_token",
      "title": "EUCALYPTUS SCENTED HAND SANITIZER (ALCOHOL) LIQUID [FOURSTAR GROUP USA, INC.]",
      "spl_version": "2",
      "published_date": "2025-02-27"
    }
  },
  "productid": "0220-1937_16f13c97-0916-a642-e063-6294a90a209c",
  "productndc": "0220-1937",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "EUCALYPTUS GLOBULUS LEAF",
  "proprietary_name": "Eucalyptus globulus",
  "active_ingred_unit": "[kp_C]/200[kp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "EUCALYPTUS GLOBULUS LEAF",
  "start_marketing_date": "20240101",
  "active_numerator_strength": "200"
}

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