Eucalyptus oil
Identification
- Summary
Eucalyptus oil is an ingredient used in a variety of natural health products.
- Brand Names
- Vaporex, Vicks Vaporub
- Generic Name
- Eucalyptus oil
- DrugBank Accession Number
- DB11114
- Background
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.
- Type
- Biotech
- Groups
- Approved
- Synonyms
- Blue gum leaf oil
- Dinkum oil
- Eucalypti aetheroleum
- Eucalyptus essential oil
- Eucalyptus globulus leaf essential oil
- Eucalyptus globulus leaf oil
- Eucalyptus globulus leaf water
- Eucalyptus globulus leaf/twig oil
- Eucalyptus globulus oil
- Eucalyptus globulus oil burundia
- Eucalyptus globulus oil pakistan
- Eucalyptus globulus oil rwanda
- Eucalyptus globulus oil zambia
- Eucalyptus leaf oil
- Eucalyptus oil
- Eucalyptus terpene oil
- Eucalyptus volatile oil
- Eukalyptus oel
- Oil of eucalyptus
- Southern blue gum leaf oil
- Tasmanian blue gum leaf oil
- External IDs
- Caswell No. 618A
- Fema no. 2466
Pharmacology
- 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 24.
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Indication Type Indication Combined Product Details Approval Level Age Group Patient Characteristics Dose Form Used in combination for symptomatic treatment of Coughing Combination Product in combination with: Camphor (DB01744), Levomenthol (DB00825) ••• ••• ••••••• •••••••• Used in combination for symptomatic treatment of Coughing Combination Product in combination with: Turpentine (DB11120), Thymol (DB02513), Camphor (DB01744), Levomenthol (DB00825) ••• ••• •••••••• Used in combination for prophylaxis of Infection Combination Product in combination with: Tea tree oil (DB11218), Lavender oil (DB14566) ••• ••• ••••• Used in combination to treat Itching caused by insect bites Combination Product in combination with: Methyl salicylate (DB09543), Zinc oxide (DB09321), Levomenthol (DB00825), Cajuput oil (DB15922), Thymol (DB02513) ••• ••• •••••••• Treatment of Nasal congestion ••• ••• •••••••• - Associated Therapies
- Contraindications & Blackbox Warnings
- Prevent Adverse Drug Events TodayTap into our Clinical API for life-saving information on contraindications & blackbox warnings, population restrictions, harmful risks, & more.Avoid life-threatening adverse drug events with our Clinical API
- Pharmacodynamics
Lipophilic monoterpene formulations of eucalyptus oil appear to be readily absorbed orally, with a primarily oxidative metabolism that might necessitate induction of the cytochrome P450 enzyme system and subsequent urinary excretion 6. Gastrointestinal absorption of eucalyptus appears to be rapid and may be enhanced by the intake of lipids and milk. 1,8-cineole (which makes up to as much as 90% of most commonly used cineole-based eucalyptus oils) 4 has also been found in vitro and in animals to possess cytochrome P450 inducing activity 7,8,9.
- Mechanism of action
The general consensus is that the exact mechanism of action of eucalyptus oil is largely unknown at this time but comprises various hypotheses from various studies.
Cineol containing preparations of eucalyptus oil may contain up to 80% (or more) 1,8-cineole 13 and is one of the most common types of eucalyptus oil formulations used. As an active agent indicated for relieving certain cold symptoms and/or certain muscular sprains and cramps, it is believed that eucalyptus oil may possess some antimicrobial and anti-inflammatory activities.
Some in vitro studies of human blood monocytes suggest a dose-dependent effect of eucalyptus oil to elicit significant inhibition of multiple cytokines, perhaps in the treatment of airway inflammation 14,15. Moreover, other studies in animal models discuss the possibility of eucalyptus oil demonstrating anti-inflammatory and anti-nociceptive effects that potentially account for inhibiting the formation of prostaglandins and cytokines by stimulated monocytes in vitro 16,17.
Furthermore, additional studies have observed eucalyptus oil anti-viral activity against herpes simplex virus (HSV-1, HSV-2) in cell cultures as well as the demonstration of broad antimicrobial activity of eucalyptus medicinal plant extracts against Alicyclobacillus acidoterretris, Bacillus cereus, E. coli, Enterococcus faecalis, MRSA, Propionibacterium acnes, S. aureus, fungus including C. albicans isolates, Trichophyton mentagrophytes, and other Gram-positive bacteria. Specific activity against periodontopathic bacteria, such as Porphyromonas gingivalis, Actinobacillus actinomycetemcomitans, Fusobacterium nucleatum, Streptococcus mutans, and Streptococcus sobrinus has also been observed 18,19,20,21,22.
- Absorption
Common monoterpenoid compound preparations of eucalyptus oil have been observed to be readily absorbed after dermal application, likely due to their lipophilic character 5. Although maximal plasma levels were demonstrated in as short a time period as 10 minutes even with thicker preparations like eucalyptus oil ointments, like many other topically applied agents, the extent of absorption is also likely largely dependent upon additional factors like the size of treated skin area, patient skin condition(s), concentrations of the applied substance, and time of exposure to the substance 5.
Currently, more data regarding the oral absorption of eucalyptus would be useful, given the relative lack of existing information 5. Lipophilic monoterpene compound formulations of eucalyptus oil seems to be readily absorbed orally 6. Regardless, there is some data that suggests that the upper part of the gastrointestinal tract has no particularly significant role in the absorption of cineole based eucalyptus oil 5.
Pulmonary absorption of eucalyptus oil is also possible although little information exists regarding this element at the moment. Nevertheless, 1,8-cineol (which makes up to as much as 90% of most commonly used cineole-based eucalyptus oils) 4 appears to be well absorbed via inhalation with peak plasma levels observed reportedly at 18 minutes 10.
Given the three main constituents from Eucalyptus globulus Labill fruits, the intestinal absorption of macrocarpal A (M-A), macrocarpal B (M-B), and cypellocarpa C (Cy-C) is predominantly via passive diffusion while Cy-C demonstrates some partly ATP-dependent absorption 12.
- Volume of distribution
Studies have determined a large terminal volume of distribution for cineole or eucalyptol (which makes up to as much as 90% of most commonly used cineole-based eucalyptus oils) of 27 l/kg in brushtail possum (Trichosurus vulpecula) 4.
- Protein binding
Not Available
- Metabolism
With in vivo models, eucalyptol or cineole (which make up to as much as 90% of most commonly used cineole-based eucalyptus oils), undergoes oxidation to form hydroxycineole which is excreted as glucuronide 23. In rats, 2-hydroxycineole, 3-hydroxycineole, and 1,8--dihydroxycineol-9-oic acid were identified as main urinary metabolites 23. After oral administration to brushtail possums, p-cresol, 9-hydroxycineole, and Cineole-9-oic acid were found in urine 23. Rabbits given eucalyptol by savage excreted 2-exo- and 2-endo-hydroxycineole in the urine 23.
The monterpene bicyclic ketone verbenone is a known component in eucalyptus globules 11. In one study, this component was observed to be converted to 10-hydroxyverbenone by rat and human liver microsomal cytochrome P450 enzymes, and indicated that CYP2A6 is a principal enzyme in verbenone hydroxylation in humans 11.
- Route of elimination
Studies suggest the route of elimination for cineole or eucalyptol (which makes up to as much as 90% of most commonly used cineole-based eucalyptus oils) in brushtail possum (Trichosurus vulpecula), rats, and rabbit subjects as being in the urine 4.
- Half-life
Studies have determined a terminal half-life for cineole or eucalyptol (which makes up to as much as 90% of most commonly used cineole-based eucalyptus oils) of approximately 7h in brushtail possum (Trichosurus vulpecula) 4.
- Clearance
Studies have determined a high clearance rate for cineole or eucalyptol (which makes up to as much as 90% of most commonly used cineole-based eucalyptus oils) of 43 ml/min/kg in brushtail possum (Trichosurus vulpecula) 4.
- Adverse Effects
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- Toxicity
Overdose with eucalyptus oil may result in epigastric burning, nausea and vomiting, dizziness, muscular weakness, mitosis, tachycardia, a sensation of suffocation, cyanosis, ataxia, pulmonary damage, delirium, convulsions, CNS depression, coma. Deaths have been recorded from doses as low as 3.5 ml.
The given oral LD50 for rats is 2480 mg/kg MSDS
- Pathways
- Not Available
- Pharmacogenomic Effects/ADRs Browse all" title="About SNP Mediated Effects/ADRs" id="snp-actions-info" class="drug-info-popup" href="javascript:void(0);">
- Not Available
Interactions
- Drug Interactions Learn More" title="About Drug Interactions" id="structured-interactions-info" class="drug-info-popup" href="javascript:void(0);">
- This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Drug Interaction Integrate drug-drug
interactions in your softwareAbacavir Abacavir may decrease the excretion rate of Eucalyptus oil which could result in a higher serum level. Aceclofenac Aceclofenac may decrease the excretion rate of Eucalyptus oil which could result in a higher serum level. Acemetacin Acemetacin may decrease the excretion rate of Eucalyptus oil which could result in a higher serum level. Acetaminophen Acetaminophen may decrease the excretion rate of Eucalyptus oil which could result in a higher serum level. Acetazolamide Acetazolamide may increase the excretion rate of Eucalyptus oil which could result in a lower serum level and potentially a reduction in efficacy. - Food Interactions
- No interactions found.
Products
- Drug product information from 10+ global regionsOur datasets provide approved product information including:dosage, form, labeller, route of administration, and marketing period.Access drug product information from over 10 global regions.
- Over the Counter Products
Name Dosage Strength Route Labeller Marketing Start Marketing End Region Image Eucalyptus Oil Liquid Topical Dawson Traders Ltd. 1977-12-31 2006-03-22 Canada Eucalyptus Oil Liquid Respiratory (inhalation) Regal Pharms, Division Of Bradcan Corporation 1983-12-31 1998-07-29 Canada Eucalyptus Oil Liquid Oral; Respiratory (inhalation); Topical Stanley Pharmaceuticals, A Division Of Vita Health Products Inc. 1972-12-31 2000-07-27 Canada Eucalyptus Oil Liq 100% Liquid 100 % Oral; Respiratory (inhalation); Topical Jedmon Products Ltd. 1990-12-31 2006-03-22 Canada EUKY BEAR BRAND EUCALYPTUS OIL BP Oil 100 % Cutaneous; Respiratory (inhalation) ROSLIND ENTERPRISE (M) SDN. BHD. 2020-09-08 Not applicable Malaysia - Mixture Products
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image 24/7 Life Medicated Chest Rub Eucalyptus oil (1.2 g/100g) + Menthol (2.6 g/100g) + Synthetic camphor (4.8 g/100g) Ointment Topical Lil' Drug Store Products, Inc. 2022-11-11 Not applicable US 4Jointz Eucalyptus oil (4 g/100g) + Allantoin (0.025 g/100g) + Tannic acid (5 g/100g) Cream Topical Arp(usa) Pty Ltd 2017-01-31 2018-04-05 US 4oz Medicated Chest Rub Eucalyptus oil (1 g/100g) + Menthol (1 g/100g) + Synthetic camphor (4.7 g/100g) Ointment Topical Pride Products Corporation 2017-12-01 Not applicable US Aboniki Balm - Topical Pain Relief Balm Eucalyptus oil (23 mg/1g) + Menthol (51 mg/1g) + Methyl salicylate (42.5 mg/1g) + Synthetic camphor (50.4 mg/1g) Cream Topical J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD 2022-06-01 Not applicable US Aldamed Eucalyptus oil (1 mg/100mL) + Menthol (2 mg/100mL) + Synthetic camphor (3 mg/100mL) Cream Topical Herbamedicus, s.r.o. 2023-03-21 Not applicable US - Unapproved/Other Products
Name Ingredients Dosage Route Labeller Marketing Start Marketing End Region Image Cellskin Clean Pine Mist Eucalyptus oil (0.01 g/100mL) + Grapefruit (0.05 g/100mL) + Tea tree oil (0.01 g/100mL) Spray Topical Gtg Wellness Co., Ltd. 2020-07-01 Not applicable US Dona Eucalyptus oil (5 mg/100mg) + Menthol (10 mg/100mg) Patch Topical Sj Incorporation Ltd 2023-11-20 Not applicable US Elmore Oil Eucalyptus oil (38.6 mg/1mL) + Tea tree oil (42.5 mg/1mL) Oil Topical Elmore Oil Company Pty Ltd 2013-07-01 Not applicable US Elmore Oil Eucalyptus oil (38.6 mg/1mL) + Tea tree oil (42.5 mg/1mL) Oil Topical Ultra Mix (Aust) Pty Ltd 2015-02-16 Not applicable US Golf Pain Away GPA Eucalyptus oil (38.6 mg/1mL) + Tea tree oil (42.5 mg/1mL) Oil Topical Elmore Oil Company Pty Ltd 2012-06-01 Not applicable US
Categories
- Drug Categories
- Classification
- Not classified
- Affected organisms
- Humans and other mammals
Chemical Identifiers
- UNII
- 2R04ONI662
- CAS number
- 8000-48-4
References
- General References
- Jun YS, Kang P, Min SS, Lee JM, Kim HK, Seol GH: Effect of eucalyptus oil inhalation on pain and inflammatory responses after total knee replacement: a randomized clinical trial. Evid Based Complement Alternat Med. 2013;2013:502727. doi: 10.1155/2013/502727. Epub 2013 Jun 18. [Article]
- Serafino A, Sinibaldi Vallebona P, Andreola F, Zonfrillo M, Mercuri L, Federici M, Rasi G, Garaci E, Pierimarchi P: Stimulatory effect of Eucalyptus essential oil on innate cell-mediated immune response. BMC Immunol. 2008 Apr 18;9:17. doi: 10.1186/1471-2172-9-17. [Article]
- Bachir RG, Benali M: Antibacterial activity of the essential oils from the leaves of Eucalyptus globulus against Escherichia coli and Staphylococcus aureus. Asian Pac J Trop Biomed. 2012 Sep;2(9):739-42. doi: 10.1016/S2221-1691(12)60220-2. [Article]
- McLean S, Boyle RR, Brandon S, Davies NW, Sorensen JS: Pharmacokinetics of 1,8-cineole, a dietary toxin, in the brushtail possum (Trichosurus vulpecula): significance for feeding. Xenobiotica. 2007 Sep;37(9):903-22. doi: 10.1080/00498250701570277. [Article]
- Kohlert C, van Rensen I, Marz R, Schindler G, Graefe EU, Veit M: Bioavailability and pharmacokinetics of natural volatile terpenes in animals and humans. Planta Med. 2000 Aug;66(6):495-505. doi: 10.1055/s-2000-8616. [Article]
- McLean S, Foley WJ: Metabolism of Eucalyptus terpenes by herbivorous marsupials. Drug Metab Rev. 1997 Feb-May;29(1-2):213-8. [Article]
- Jori A, Bianchetti A, Prestini PE, Gerattini S: Effect of eucalyptol (1,8-cineole) on the metabolism of other drugs in rats and in man. Eur J Pharmacol. 1970 Mar;9(3):362-6. [Article]
- Pass GJ, McLean S, Stupans I, Davies N: Microsomal metabolism of the terpene 1,8-cineole in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus), rat and human. Xenobiotica. 2001 Apr;31(4):205-21. doi: 10.1080/00498250110043535 . [Article]
- Miyazawa M, Shindo M, Shimada T: Oxidation of 1,8-cineole, the monoterpene cyclic ether originated from eucalyptus polybractea, by cytochrome P450 3A enzymes in rat and human liver microsomes. Drug Metab Dispos. 2001 Feb;29(2):200-5. [Article]
- Jager W, Nasel B, Nasel C, Binder R, Stimpfl T, Vycudilik W, Buchbauer G: Pharmacokinetic studies of the fragrance compound 1,8-cineol in humans during inhalation. Chem Senses. 1996 Aug;21(4):477-80. [Article]
- Miyazawa M, Sugie A, Shimada T: Roles of human CYP2A6 and 2B6 and rat CYP2C11 and 2B1 in the 10-hydroxylation of (-)-verbenone by liver microsomes. Drug Metab Dispos. 2003 Aug;31(8):1049-53. doi: 10.1124/dmd.31.8.1049. [Article]
- Yang XW, Guo QM, Wang Y, Xu W, Tian L, Tian XJ: Intestinal permeability of antivirus constituents from the fruits of Eucalyptus globulus Labill. in Caco-2 Cell Model. Bioorg Med Chem Lett. 2007 Feb 15;17(4):1107-11. doi: 10.1016/j.bmcl.2006.11.021. Epub 2006 Nov 10. [Article]
- Schnitzler P, Schon K, Reichling J: Antiviral activity of Australian tea tree oil and eucalyptus oil against herpes simplex virus in cell culture. Pharmazie. 2001 Apr;56(4):343-7. [Article]
- Juergens UR, Stober M, Vetter H: Inhibition of cytokine production and arachidonic acid metabolism by eucalyptol (1.8-cineole) in human blood monocytes in vitro. Eur J Med Res. 1998 Nov 17;3(11):508-10. [Article]
- Juergens UR, Stober M, Schmidt-Schilling L, Kleuver T, Vetter H: Antiinflammatory effects of euclyptol (1.8-cineole) in bronchial asthma: inhibition of arachidonic acid metabolism in human blood monocytes ex vivo. Eur J Med Res. 1998 Sep 17;3(9):407-12. [Article]
- Santos FA, Rao VS: Antiinflammatory and antinociceptive effects of 1,8-cineole a terpenoid oxide present in many plant essential oils. Phytother Res. 2000 Jun;14(4):240-4. [Article]
- Atta AH, Alkofahi A: Anti-nociceptive and anti-inflammatory effects of some Jordanian medicinal plant extracts. J Ethnopharmacol. 1998 Mar;60(2):117-24. [Article]
- Sartorelli P, Marquioreto AD, Amaral-Baroli A, Lima ME, Moreno PR: Chemical composition and antimicrobial activity of the essential oils from two species of Eucalyptus. Phytother Res. 2007 Mar;21(3):231-3. doi: 10.1002/ptr.2051. [Article]
- Ahmad I, Beg AZ: Antimicrobial and phytochemical studies on 45 Indian medicinal plants against multi-drug resistant human pathogens. J Ethnopharmacol. 2001 Feb;74(2):113-23. [Article]
- Takahashi T, Kokubo R, Sakaino M: Antimicrobial activities of eucalyptus leaf extracts and flavonoids from Eucalyptus maculata. Lett Appl Microbiol. 2004;39(1):60-4. doi: 10.1111/j.1472-765X.2004.01538.x. [Article]
- Osawa K, Yasuda H, Morita H, Takeya K, Itokawa H: Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus. J Nat Prod. 1996 Sep;59(9):823-7. doi: 10.1021/np9604994. [Article]
- Takarada K, Kimizuka R, Takahashi N, Honma K, Okuda K, Kato T: A comparison of the antibacterial efficacies of essential oils against oral pathogens. Oral Microbiol Immunol. 2004 Feb;19(1):61-4. [Article]
- Safety Assessment of Eucalyptus globulus (Eucalyptus) - Derived Ingredients as Used in Cosmetics [Link]
- Electronic Medicines Compendium: Eucalyptus Oil BP Monograph [Link]
- Sigma-Aldrich: Eucalyptus oil Profile [Link]
- External Links
- PubChem Substance
- 347911122
- 59087
- Wikipedia
- Eucalyptus_oil
- MSDS
- Download (47.5 KB)
Clinical Trials
- Clinical Trials Learn More" title="About Clinical Trials" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">
Phase Status Purpose Conditions Count 4 Completed Treatment Tonsillopharyngitis / Viral Respiratory Tract Infection 1 2 Completed Treatment Coronavirus Disease 2019 (COVID‑19) 1 2, 3 Recruiting Treatment Hepatocellular Carcinoma 1 1 Completed Diagnostic Gingivitis / Plaque, Dental 1
Pharmacoeconomics
- Manufacturers
- Not Available
- Packagers
- Not Available
- Dosage Forms
Form Route Strength Liquid Respiratory (inhalation) 6 % Oil Percutaneous; Topical; Transdermal Ointment Respiratory (inhalation); Topical Ointment Respiratory (inhalation) Spray Topical Oil Mouthwash Dental Liquid Respiratory (inhalation) 1 %w/v Liquid Oral; Respiratory (inhalation); Topical Liquid Respiratory (inhalation) Liquid Topical Liquid Oral; Respiratory (inhalation); Topical 100 % Oil Cutaneous; Respiratory (inhalation) 100 % Lozenge Oral Tablet Solution Topical Liniment Topical Oil Topical; Transdermal Tablet Oral Oil Topical Liquid Respiratory (inhalation) Jelly Topical Stick Topical Cream Topical Oil Topical Liquid Topical Patch Cutaneous; Topical; Transdermal Patch Topical Lotion Topical Gel Topical Plaster Cutaneous Plaster Plaster Topical Cream Cutaneous Salve Topical Ointment Cutaneous Ointment Topical Ointment Topical 5 % Gum, chewing Oral Aerosol Respiratory (inhalation) 100 ml/100ml Oil Nasal 100 ml/100ml Oil Topical 100 ml/100ml - Prices
- Not Available
- Patents
- Not Available
Properties
- State
- Not Available
- Experimental Properties
- Not Available
Drug created at December 03, 2015 16:51 / Updated at February 20, 2024 23:55