Eucalyptus Globulus

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
3766206811
200 PELLET in 1 VIAL, GLASS (37662-0681-1)
ndc11
3766206812
1200 PELLET in 1 BOTTLE, GLASS (37662-0681-2)
ndc11
3766206813
4000 PELLET in 1 BOTTLE, GLASS (37662-0681-3)

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": "37662-0681_e1fe022c-d1db-183a-e053-2995a90ae17f",
  "productndc": "37662-0681",
  "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]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Eucalyptus Globulus",
  "start_marketing_date": "20220621",
  "active_numerator_strength": "6"
}

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