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United States · US · US:0220-1940_16f1551c-c806-c294-e063-6394a90a67f3
Eucalyptus globulus
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBoiron
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11022019404130 [hp_C] in 1 TUBE (0220-1940-41)
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": "0220-1940_16f1551c-c806-c294-e063-6394a90a67f3",
"productndc": "0220-1940",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "EUCALYPTUS GLOBULUS LEAF",
"proprietary_name": "Eucalyptus globulus",
"active_ingred_unit": "[hp_C]/30[hp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "EUCALYPTUS GLOBULUS LEAF",
"start_marketing_date": "19830303",
"active_numerator_strength": "30"
}Access this data programmatically
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