CAJEPUT OIL

OTHER NAME(S):

Aceite de Cajeput, Cajeputi Aetheroleum, Cajeputier, Essence de Caia-Pouti, Essence de Cajeput, Huile de Cajoupouli, Huile de Cajeput, Kajuput, Kajuputi leucadendra, Kayaputi, Melaleuca leucadendra, Melaleuca Leucodendron, Melaleuca quinquenervia, Myrtus leucadendra, Paperbark Tree Oil, Punk Tree.<br/><br/>

Overview

Overview Information

Cajeput oil is produced by steam distillation of fresh leaves and twigs of the cajeput tree (Melaleuca leucadendra) and the paperbark tree (Melaleuca quinquenervia). Don’t confuse cajeput oil with tea tree oil (Melaleuca alternifolia) or niauli oil (Melaleuca viridiflora).

Cajeput oil is used to treat colds, headaches, toothache, and tumors; to loosen phlegm so it can be coughed up (as an expectorant); and as a tonic.

Some people apply cajeput oil to the skin for mites (scabies) and a fungal infection of the skin (tinea versicolor).

Cajeput oil is also used either alone or in combination with other ingredients in commercially available antiseptic lotions to treat joint pain (rheumatism) and other pains.

Some people inhale cajeput oil as an expectorant.

In dentistry, cajeput oil is used to relieve gum pain after a tooth is removed or lost.

In food and beverages, cajeput oil is used as a flavoring in very small amounts.

How does it work?

Cajeput oil contains a chemical called cineole. When applied to the skin, cineole can cause surface warmth and irritation, which relieves pain beneath the skin.

Uses

Uses & Effectiveness?

Insufficient Evidence for

  • Toothache.
  • Colds.
  • Headaches.
  • Tumors.
  • Use as a tonic.
  • Thinning mucous (congestion) and making it easier to cough up, when taken by mouth or inhaled.
  • Fungal skin infections, when applied to the skin.
  • Joint pain (rheumatism), when applied to the skin.
  • Other conditions.
More evidence is needed to rate the effectiveness of cajeput oil for these uses.

Side Effects

Side Effects & Safety

Very small amounts of cajeput oil are LIKELY SAFE when added to food as flavoring, but the safety of taking larger amounts by mouth is unknown.

Cajeput oil is POSSIBLY SAFE for most people when applied in medicinal amounts to unbroken skin, but it can cause allergic reactions.

It is POSSIBLY UNSAFE to inhale cajeput oil. It can cause breathing problems.

Special Precautions & Warnings:

Pregnancy and breast-feeding: There is not enough reliable information about the safety of taking cajeput oil if you are pregnant or breast-feeding. Stay on the safe side and avoid use.

Children: Cajeput oil is LIKELY UNSAFE when inhaled or applied to the faces of children. It can cause serious breathing problems.

Asthma: Inhaling cajeput oil might cause an asthma attack.

Interactions

Interactions?

We currently have no information for CAJEPUT OIL Interactions.

Dosing

Dosing

The appropriate dose of cajeput oil for use as treatment depends on several factors such as the user's age, health, and several other conditions. At this time there is not enough scientific information to determine an appropriate range of doses for cajeput oil. Keep in mind that natural products are not always necessarily safe and dosages can be important. Be sure to follow relevant directions on product labels and consult your pharmacist or physician or other healthcare professional before using.

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View References

REFERENCES:

  • Amer, A. and Mehlhorn, H. Repellency effect of forty-one essential oils against Aedes, Anopheles, and Culex mosquitoes. Parasitol.Res 2006;99(4):478-490. View abstract.
  • Bhamarapravati, S., Pendland, S. L., and Mahady, G. B. Extracts of spice and food plants from Thai traditional medicine inhibit the growth of the human carcinogen Helicobacter pylori. In Vivo 2003;17(6):541-544. View abstract.
  • El Toumy, S. A., Marzouk, M. S., Moharram, F. A., and Aboutabl, E. A. Flavonoids of Melaleuca quinquenervia. Pharmazie 2001;56(1):94-95. View abstract.
  • Hiermann, A. and Bucar, F. Influence of some traditional medicinal plants of Senegal on prostaglandin biosynthesis. J Ethnopharmacol 1994;42(2):111-116. View abstract.
  • Jedlickova, Z., Mottl, O., and Sery, V. Antibacterial properties of the Vietnamese cajeput oil and ocimum oil in combination with antibacterial agents. J Hyg Epidemiol.Microbiol.Immunol 1992;36(3):303-309. View abstract.
  • Lee, C. K. A New Norlupene from the Leaves of Melaleuca leucadendron. J Nat Prod. 3-27-1998;61(3):375-376. View abstract.
  • Lee, C. K. and Chang, M. H. Four new triterpenes from the heartwood of melaleuca leucadendron. J Nat Prod. 1999;62(7):1003-1005. View abstract.
  • Lee, T. H., Wang, G. J., Lee, C. K., Kuo, Y. H., and Chou, C. H. Inhibitory effects of glycosides from the leaves of Melaleuca quinquenervia on vascular contraction of rats. Planta Med 2002;68(6):492-496. View abstract.
  • LOCKHART, C., AUSTIN, D. F., and AUMEN, N. G. Water Level Effects on Growth of Melaleuca Seedlings from Lake Okeechobee (Florida, USA) Littoral Zone. Environ.Manage. 1999;23(4):507-518. View abstract.
  • Moharram, F. A., Marzouk, M. S., El Toumy, S. A., Ahmed, A. A., and Aboutabl, E. A. Polyphenols of Melaleuca quinquenervia leaves--pharmacological studies of grandinin. Phytother Res 2003;17(7):767-773. View abstract.
  • Mueller, R. S., Bettenay, S. V., and Tideman, L. Aero-allergens in canine atopic dermatitis in southeastern Australia based on 1000 intradermal skin tests. Aust Vet.J 2000;78(6):392-399. View abstract.
  • Muller, J. F., Hawker, D. W., McLachlan, M. S., and Connell, D. W. PAHs, PCDD/Fs, PCBs and HCB in leaves from Brisbane, Australia. Chemosphere 2001;43(4-7):507-515. View abstract.
  • Nawawi, A., Nakamura, N., Hattori, M., Kurokawa, M., and Shiraki, K. Inhibitory effects of Indonesian medicinal plants on the infection of herpes simplex virus type 1. Phytother Res 1999;13(1):37-41. View abstract.
  • Oelrichs, P. B., MacLeod, J. K., Seawright, A. A., and Grace, P. B. Isolation and identification of the toxic peptides from Lophyrotoma zonalis (Pergidae) sawfly larvae. Toxicon 2001;39(12):1933-1936. View abstract.
  • Quimby, P. C., Jr., DeLoach, C. J., Wineriter, S. A., Goolsby, J. A., Sobhian, R., Boyette, C. D., and Abbas, H. K. Biological control of weeds: research by the United States Department of Agriculture-Agricultural Research Service: selected case studies. Pest.Manag.Sci 2003;59(6-7):671-680. View abstract.
  • Stablein, J. J., Bucholtz, G. A., and Lockey, R. F. Melaleuca tree and respiratory disease. Ann.Allergy Asthma Immunol. 2002;89(5):523-530. View abstract.
  • Stanaland, B. E., Gennaro, R. N., Bausher, M. G., Klotz, S. D., White, R. S., and Sweeney, M. J. Allergenic cross-reactivity between Callistemon citrinis and Melaleuca quinquenervia pollens. Int Arch Allergy Appl Immunol 1988;86(1):35-41. View abstract.
  • Stanaland, B. E., Gennaro, R. N., Klotz, S. D., Sweeney, M. J., and White, R. S. Isolation and characterization of cross-reactive allergenic components in Callistemon citrinis and Melaleuca quinquenervia pollen by trans-blot enzyme-linked crossed immunoelectrophoresis. Int Arch Allergy Appl Immunol 1986;80(3):278-284. View abstract.
  • Subehan, Usia, T., Iwata, H., Kadota, S., and Tezuka, Y. Mechanism-based inhibition of CYP3A4 and CYP2D6 by Indonesian medicinal plants. J Ethnopharmacol. 5-24-2006;105(3):449-455. View abstract.
  • Sweeney, M., Hosseiny, S., Hunter, S., Klotz, S. D., Gennaro, R. N., and White, R. S. Immunodetection and comparison of melaleuca, bottlebrush, and bahia pollens. Int Arch Allergy Immunol 1994;105(3):289-296. View abstract.
  • Tsuruga, T., Chun, Y. T., Ebizuka, Y., and Sankawa, U. Biologically active constituents of Melaleuca leucadendron: inhibitors of induced histamine release from rat mast cells. Chem Pharm Bull.(Tokyo) 1991;39(12):3276-3278. View abstract.
  • Wheeler, G. S., Massey, L. M., and Southwell, I. A. Dietary influences on terpenoids sequestered by the biological control agent Oxyops vitiosa: effect of plant volatiles from different Melaleuca quinquenervia chemotypes and laboratory host species. J Chem Ecol 2003;29(1):189-208. View abstract.
  • Electronic Code of Federal Regulations. Title 21. Part 182 -- Substances Generally Recognized As Safe. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=182
  • Franklyn AJ, Bettenridge J, Daykin J, et al. Long-term thyroxine treatment and bone mineral density. Lancet 1992;340:9-13. View abstract.
  • Osol and Farar. The Dispensatory of the United States of America. 25th ed. JB Lippincott Co., 1955.

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CONDITIONS OF USE AND IMPORTANT INFORMATION: This information is meant to supplement, not replace advice from your doctor or healthcare provider and is not meant to cover all possible uses, precautions, interactions or adverse effects. This information may not fit your specific health circumstances. Never delay or disregard seeking professional medical advice from your doctor or other qualified health care provider because of something you have read on WebMD. You should always speak with your doctor or health care professional before you start, stop, or change any prescribed part of your health care plan or treatment and to determine what course of therapy is right for you.

This copyrighted material is provided by Natural Medicines Comprehensive Database Consumer Version. Information from this source is evidence-based and objective, and without commercial influence. For professional medical information on natural medicines, see Natural Medicines Comprehensive Database Professional Version.
© Therapeutic Research Faculty 2018.