MedPath

Eucalyptus oil

Generic Name
Eucalyptus oil
Brand Names
Vaporex, Vicks Vaporub
Drug Type
Biotech
CAS Number
8000-48-4
Unique Ingredient Identifier
2R04ONI662

Overview

Eucalyptus oil is a distilled oil derived from the leaves of the tree Eucalyptus. It is shown to be effective in reducing pain, swelling, and inflammation via its modulatory effect on the immune response. It is also shown to exhibit antibacterial activity against some bacterial species and cough suppressant actions. Eucalyptus oil can be applied directly to the skin for pain and swelling of respiratory tract mucous membranes, joint pain, genital herpes, and nasal stuffiness.

Indication

As an active agent, eucalyptus oil has been indicated for relief of the symptoms of catarrhal colds, and/or the relief of the symptoms of minor muscular sprains and cramps .

Associated Conditions

  • Cough
  • Infection
  • Itching caused by Insect Bites
  • Myalgia
  • Nasal Congestion
  • Pruritis of the skin
  • Rash caused by Insect Bites
  • Infection in minor cuts, scrapes, or burns
  • Minor aches and pains

Clinical Trials

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Kroger Co
30142-248
TOPICAL
12 mg in 1 g
4/8/2025
Walgreen Company
0363-9802
TOPICAL
12 mg in 1 g
7/31/2025
Old East Main CO.
55910-248
TOPICAL
1.2 kg in 100 kg
8/12/2025
Neilmed Pharmaceuticals Inc.
13709-336
TOPICAL
0.012 g in 1 g
7/4/2025
Ultra Mix (Aust) Pty Ltd
69594-004
TOPICAL
38.6 mg in 1 g
2/16/2015
LJ Pharma
84809-007
TOPICAL
1.2 g in 100 g
8/1/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
HALLS MENTHO LYPTUS COUGH TAB BLACK CURRANT
adams canada, division of warner-lambert canada inc.
00627070
Lozenge - Oral
6.5 MG / LOZ
12/31/1984
HERBON COUGH DROPS GLACIAL MINT
herbon naturals inc.
02231756
Drops - Oral
0.2 MG / DROP
9/8/1997
BENTASIL EXTRA STRENGTH EUCALYPTUS
carter-horner corp.
02240046
Lozenge - Oral
5.6 MG / LOZ
8/30/1999
EUCALYPTUS OIL
stanley pharmaceuticals, a division of vita health products inc.
00238619
Liquid - Oral ,  Inhalation ,  Topical
null NIL / NIL
12/31/1972
RUBBEX CREME
vitalab
00840815
Cream - Topical
.52 %
12/31/1994
HERBAL COLD RELIEF CAP
jamieson laboratories ltd
02094827
Capsule - Oral
.1 MG / CAP
12/31/1994
MEDICATED ANALGESIC CREAM
prodemdis enr.
02038196
Cream - Topical
.5 %
10/25/1996
HALLS EXTRA STRONG
warner-lambert canada inc.
02241431
Lozenge - Oral
7.25 MG / LOZ
N/A
VITALP PLUS EUCALYPTUS
domaco dr med aufdermaur ag
02237554
Lozenge - Oral
5 MG / LOZ
N/A
HALLS MENTHO-LYPTUS COUGH TABLETS PINK GRAPEFRUIT
warner-lambert canada inc.
02239421
Lozenge - Oral
4 MG / LOZ
N/A

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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