Chillout™ Tea 50g

£7.00

T’n’T Teas® Chillout Tea™ comforting herbal tea blend is a delicious and healthy tea blend that can be enjoyed by people of all ages. It is a good choice for people who are looking for a natural way to improve their sleep quality, reduce stress and anxiety, improve digestion, reduce inflammation, and improve mood.

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Description

Discover T’n’T Teas’® Chillout Tea™ – a blend that invites serenity into your cup. With a refreshing touch of mint and a hint of delicate florals, it promises a calming experience.

The Chillout Tea™ – a soothing herbal blend designed to transport you to a realm of relaxation and tranquillity. Crafted with the pure essence of spearmint and chamomile, it promises a comforting and serene experience.

The journey begins with the invigorating embrace of spearmint, a refreshing overture to a sensory adventure. Camomile takes centre stage, ushering in a wave of calm and serenity, like the hush of a quiet meadow at dawn.

Sip your way to tranquillity and relaxation with every soothing, minty infusion.

Additional information

Weight50 g

Wellbeing / Side Effects

Beyond the soothing taste, this blend may offer potential health benefits. Spearmint is known for its digestive properties, while camomile is renowned for its calming effect, promoting relaxation and tranquillity.

This tea blend is generally well-tolerated, but there are a few potential side effects to be aware of:
Spearmint: Spearmint may interact with certain medications, such as blood thinners and antacids. Additionally, pregnant and breastfeeding women should talk to their doctor before consuming spearmint.
Camomile: Chamomile may interact with certain medications, such as sedatives and tranquillisers. Additionally, pregnant and breastfeeding women should talk to their doctor before consuming camomile.

Allergens
This tea blend is naturally free of common allergens, but it is always important to check the ingredient list for specific concerns.

Contraindications
Avoid this tea blend if you have known allergies to any of the listed ingredients. Consult your healthcare provider if pregnant, nursing, or with specific health conditions. Not suitable for children under 6 years.

The Chill Out Tea™ is a 100% natural product, it does not contain allergens or impurities, and it does not contain added flavours, so its consumption should not cause unpleasant stomach upsets.

Chill Out Tea™ is a certified, premium quality professionally mixed product, made with the highest quality, medicinal natural herbs from around the world. We pay special attention to the purity of the plants, so we only buy the certified raw materials for our products from reliable, controlled sources, so we can ensure that we minimise contact with foreign substances during storage, transportation, and production.       

CAUTION: Herbs have medicinal properties and can promote the body’s physical and mental self-healing and harmonising process, but they cannot replace medical examination, care and possible treatment – so if you are on medication from your doctor, please check that they are happy for you to drink the tea. If you feel any discomfort, stop and only restart slowly if you are comfortable doing so (it might not be the herbal tea that causes the discomfort!). Pregnant or breastfeeding women, or children under the age of 12 years old, should exercise extra caution.

For a detailed description, please look at the individual ingredients.

Profile

Colour: A gentle, pale infusion that mirrors a tranquil garden.
Aroma: It’s like taking a stroll through a minty meadow, with delicate floral whispers in the breeze.
Initial taste: The first sip is a refreshing minty embrace, like a mint leaf on your tongue.
Midtones: Camomile steps in, offering a gentle, calming note, like a lullaby for your taste buds.
Aftertaste: A subtle, soothing sensation lingers, like the encore of a serene melody.
Body: It’s a light and comforting presence, like a cosy blanket for your senses.
Caffeine content: This tea blend is caffeine-free, offering serenity without any interruptions.

Ingredients

Spearmint | Camomile

In this special tea mixture, the ingredients amplify and complement each other’s effects, thanks to the synergy between them, providing the freshness and calming compounds needed to chill out and relax.

This tea contains 100% natural products without allergens or impurities, and no added flavours or colourants, so its consumption should not cause any unpleasant stomach upsets. Please refer to possible side effects in the next tab.

Shake well before use.

GMO-Free. Suitable for vegans.

Hand-blended & prepared in Shropshire, England.

The Chillout™ tea is a 100% natural product, it does not contain allergens or impurities, and it does not contain added flavours, so its consumption should not cause unpleasant stomach upsets.

Chillout™ tea, a certified, premium quality professionally mixed product, made with the highest quality, medicinal natural herbs from around the world. We pay special attention to the purity of the plants, so we only buy the certified raw materials for our products from reliable, controlled sources, so we can ensure that we minimise contact with foreign substances during storage, transportation, and production.

Certified Origins

Bulgarian flag denoting that one or more ingredients was ethically sourced from Bulgaria. Serbian flag denoting that one or more ingredients was ethically sourced from Serbia.

Hand-blended in Shropshire, England.

Preparation

“Zen Time!” – Preparation Notes for T’n’T Teas’® Chillout Tea™:

  1. Relax mode: Get into the perfect mood for tranquillity. Find your cosiest cup or teapot and prepare for some much-needed zen time.
  2. Tea delight: Scoop a teaspoon of our Chillout Tea™ blend. The minty and camomile duo is your path to serenity.
  3. Gentle warmth: Heat fresh, cold water to around 96°C (205°F). We’re making a warm hug for your senses.
  4. Soothing soak: Pour the hot water over the tea blend, like a gentle shower of calm. Let them steep for 10-15 minutes.
  5. Flavour companion: If you like, add a dollop of honey or a slice of apple for an extra layer of comfort.
  6. Zen cover: Keep your cup or teapot covered with a lid while the minty and chamomile symphony harmonises.
  7. Strain and sip: The relaxation ritual is about to commence. Strain the tea blend and immerse yourself in the soothing journey.
  8. Sip and melt: Hold your cup close and take a sip of the minty and floral serenity. It’s like wrapping yourself in a cosy blanket of flavours.
  9. Zen repeats: The zen journey doesn’t have to end after one round. Prepare for another steeping session whenever you crave tranquility.
  10. Zen for later: Store your tea blend in a serene, cool, and dry place, ready to create zen moments at your whim.

Prepare for a blissful journey to serenity with T’n’T Teas’® Chillout Tea™. Let the mint and camomile serenade you to a world of calm and tranquility.

The Chill Out Tea is an excellent drink to consume at anytime of the day, even just before bed.

Clinical References

Clinical evidence of the ingredients found in this product. These are public domain references and do not relate directly to our product.

Camomile

  • Agarwal A, Chaudhary B. Clinical and microbiological effects of 1% Matricaria chamomilla mouth rinse on chronic periodontitis: a double-blind randomized placebo-controlled trial. J Indian Soc Periodontol 2020;24(4):354-61.
  • Aitken-Saavedra J, Chaves Tarquinio SB, De Oliveira da Rosa WL, et al. Effect of a homemade salivary substitute prepared using chamomile (Matricaria chamomilla L.) flower and flax (Linum usitatissimum L.) seed to relieve primary burning mouth syndrome: a preliminary report. J Altern Complement Med 2020;26(9):799-806.
  • Amsterdam JD, Li Y, Soeller I, et al. A randomized, double-blind, placebo-controlled trial of oral Matricaria recutita (chamomile) extract therapy for generalized anxiety disorder. J Clin Psychopharmacol. 2009;29(4):378-382.
  • Avallone R, Zanoli P, Puia G, et al. Pharmacological profile of apigenin, a flavonoid isolated from Matricaria chamomilla. Biochem Pharmacol 2000;59:1387-94.
  • Barene I, Daberte I, Zvirgzdina L, Iriste V. The complex technology on products of German chamomile. Medicina (Kaunas). 2003;39(Suppl 2):127-131.
  • Becker B, Kuhn U, Hardewig-Budny B. Double-blind, randomized evaluation of clinical efficacy and tolerability of an apple pectin-chamomile extract in children with unspecific diarrhea. Arzneimittelforschung 2006;56(6):387-393.
  • Benito P, Rodríguez-Perez R, García F, Juste S, Moneo I, Caballero ML. Occupational allergic rhinoconjunctivitis induced by Matricaria chamomilla with tolerance of chamomile tea. J Investig Allergol Clin Immunol. 2014;24(5):369-70. No abstract available. View abstract.
  • Bosak Z, Iravani M, Moghimipour E, Haghighizadeh MH, Jelodarian P, Khazdair MR. Evaluation of the influence of chamomile vaginal gel on dyspareunia and sexual satisfaction in postmenopausal women: a randomized, double-blind, controlled clinical trial. Avicenna J Phytomed 2020;10(5):481-91.
  • Braga FT, Santos AC, Bueno PC, et al. Use of Chamomilla recutita in the prevention and treatment of oral mucositis in patients undergoing hematopoietic stem cell transplantation: a randomized, controlled, phase II clinical trial. Cancer Nurs 2015;38(4):322-9.
  • Buckle J. Use of aromatherapy as a complementary treatment for chronic pain. Altern Ther Health Med 1999;5:42-51.
  • Budzinski JW, Foster BC, Vandenhoek S, Arnason JT. An in vitro evaluation of human cytochrome P450 3A4 inhibition by selected commercial herbal extracts and tinctures. Phytomedicine 2000;7:273-82.
  • Carl W, Emrich LS. Management of oral mucositis during local radiation and systemic chemotherapy: a study of 98 patients. J Prosthet Dent 1991;66:361-9.
  • Charousaei F, Dabirian A, Mojab F. Using chamomile solution or a 1% topical hydrocortisone ointment in the management of peristomal skin lesions in colostomy patients: results of a controlled clinical study. Ostomy Wound Manage 2011;57:28-36.
  • Daneshfard B, Shahriari M, Heiran A, Nimrouzi M, Yarmohammadi H. Effect of chamomile on chemotherapy-induced neutropenia in pediatric leukemia patients: A randomized triple-blind placebo-controlled clinical trial. Avicenna J Phytomed. 2020;10(1):58-69.
  • Eddouks M, Lemhardri A, Zeggwagh NA, Michel JB. Potent hypoglycaemic activity of the aqueous extract of Chamaemelum nobile in normal and streptozoticin-induced diabetic rats. Diabetes Res Clin Pract 2005;67(3);189-95.
  • 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
  • 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
  • Fidler P, Loprinzi CL, O’Fallon JR, et al. Prospective evaluation of a chamomile mouthwash for prevention of 5-FU-induced oral mucositis. Cancer 1996;77:522-5.
  • Forster CF, Sussmann HE, Patzelt-Wenczler R. [Optimization of the Barron ligature treatment of 2nd and 3rd-degree hemorrhoids using a therapeutic troika]. Praxis (Bern 1994) 1996;85(46):1476-1481.
  • Ganzera M, Schneider P, Stuppner H. Inhibitory effects of the essential oil of chamomile (Matricaria recutita L.) and its major constituents on human cytochrome P450 enzymes. Life Sci 2006;78(8):856-861.
  • Garbuio DC, Ribeiro VDS, Hamamura AC, et al. A Chitosan-Coated Chamomile Microparticles Formulation to Prevent Radiodermatitis in Breast: A Double-blinded, Controlled, Randomized, Phase II Clinical Trial. Am J Clin Oncol 2022;45(5):183-189.
  • George J, Hegde S, Rajesh KS, et al. The efficacy of a herbal-based toothpaste in the control of plaque and gingivitis: a clinico-biochemical study. Indian J Dent Res 2009;20(4):480-482.
  • Glowania HJ, Raulin C, Swoboda M. [Effect of chamomile on wound healing–a clinical double-blind study]. Z Hautkr 1987;62(17):1262, 1267-1271.
  • Gomaa A, Hashem T, Mohamed M, Ashry E. Matricaria chamomilla extract inhibits both development of morphine dependence and expression of abstinence syndrome in rats. J Pharmacol Sci 2003;92:50-5.
  • Guimaraes R, Barros L, Duenas M, et al. Nutrients, phytochemicals and bioactivity of wild Roman chamomile: a comparison between the herb and its preparations. Food Chem 2013;136(2):718-25.
  • Habersang S, Leuschner F, Isaac O, Thiemer K. [Pharmacological studies with compounds of chamomile. IV. Studies on toxicity of (-)-alpha-bisabolol (author’s transl)]. Planta Med 1979;37:115-23.
  • Holtmann G, Madisch A, Juergen H, et al. A double-blind, randomized, placebo-controlled trial on the effects of an herbal preparation in patients with functional dyspepsia [Abstract]. Ann Mtg Digestive Disease Week 1999 May.
  • Hormann HP, Korting HC. Evidence for the efficacy and safety of topical herbal drugs in dermatology: part I: anti-inflammatory agents. Phytomedicine 1994;1:161-71.
  • Kabiri M, Kamalinejad M, Bioos S, Shariat M, Sohrabvand F. Comparative study of the effects of chamomile (Matricaria chamomilla L.) and cabergoline on idiopathic hyperprolactinemia: a pilot randomized controlled trial. Iran J Pharm Res 2019;18(3):1612-21.
  • Kassi E, Papoutsi Z, Fokialakis N, et al. Greek plant extracts exhibit selective estrogen receptor modulator (SERM)-like properties. J Agric Food Chem 2004;52:6956-61.
  • Kobayashi Y, Nakano Y, Inayama K, et al. Dietary intake of the flower extracts of German chamomile (Matricaria recutita L.) inhibited compound 48/80-induced itch-scratch responses in mice. Phytomedicine 2003;10:657-64.
  • Loggia RD, Traversa U, Scarcia V, et al. Depressive effects of Chamomilla recutita (L.) Rausch, tubular flowers, on central nervous system in mice. Pharmacol Res Commun 1982;14(2):153-162.
  • Lopez Jornet P, Aznar-Cayuela C. Efficacy of topical chamomile management vs. placebo in patients with oral lichen planus: a randomized double-blind study. J Eur Acad Dermatol Venereol 2016;30(10):1783-6.
  • Madisch A, Holtmann G, Mayr G, et al. Treatment of functional dyspepsia with a herbal preparation. A double-blind, randomized, placebo-controlled, multicenter trial. Digestion 2004;69:45-52.
  • Madisch A, Melderis H, Mayr G, et al. [A plant extract and its modified preparation in functional dyspepsia. Results of a double-blind placebo controlled comparative study]. Z Gastroenterol 2001;39(7):511-7.
  • Maliakal PP, Wanwimolruk S. Effect of herbal teas on hepatic drug metabolizing enzymes in rats. J Pharm Pharmacol 2001;53:1323-9.
  • Mao JJ, Xie SX, Keefe JR, Soeller I, Li QS, Amsterdam JD. Long-term chamomile (Matricaria chamomilla L.) treatment for generalized anxiety disorder: A randomized clinical trial. Phytomedicine 2016;23(14):1735-1742.
  • Martinelli M, Ummarino D, Giugliano FP, et al. Efficacy of a standardized extract of Matricariae chamomilla L., Melissa officinalis L. and tyndallized Lactobacillus acidophilus (HA122) in infantile colic: an open randomized controlled trial. Neurogastroenterol Motil. 2017 Dec;29:e13145.
  • Melzer J, Rosch W, Reichling J, et al. Meta-analysis: phytotherapy of functional dyspepsia with the herbal drug preparation STW 5 (Iberogast). Aliment Pharmacol Ther 2004;20:1279-87.
  • Menêses AG, Ferreira EB, Bontempo PSM, Guerra ENS, Reis PEDD. Use of Chamomile Infusion to Mitigate Radiotherapy-Induced Dry Desquamation in Head and Neck Cancer Patients. Integr Cancer Ther 2022;21:15347354221105491.
  • Mostafapour Kandelous H, Salimi M, Khori V, Rastkari N, Amanzadeh A, Salimi M. Mitochondrial apoptosis induced by Chamaemelum nobile extract in breast cancer cells. Iran J Pharm Res 2016;15(Suppl):197-204.
  • Nemati S, Yousefbeyk F, Ebrahimi SM, FaghihHabibi A, Shakiba M, Ramezani H. Effects of chamomile extract nasal drop on chronic rhinosinusitis treatment: A randomized double-blind study. Am J Otolaryngol 2021;42(1):102743.
  • Patzelt-Wenczler R, Ponce-Poschl E. Proof of efficacy of Kamillosan cream in atopic eczema. Eur J Med Res 2000;5:171-175.
  • Pirzad A, Alyari H, Shakiba RM, Zehtab-Salmasi S, and Mohammadi SA. Essential Oil Content and Composition of German Chamomile ( Matricaria chamomilla L. ) at Different Irrigation Regimes. Journal of Agronomy. 03/2006; 5(3).
  • Robbers JE, Tyler VE. Tyler’s Herbs of Choice: The Therapeutic Use of Phytomedicinals. New York, NY: The Haworth Herbal Press, 1999.
  • Saghafi N, Rhkhshandeh H, Pourmoghadam N, et al. Effectiveness of Matricaria chamomilla (chamomile) extract on pain control of cyclic mastalgia: a double-blind randomised controlled trial. J Obstet Gynaecol 2018;38(1):81-4.
  • Sahebnasagh M, Aksi V, Eslami F, et al. Prevention of radiotherapy-related oral mucositis with zinc and polyherbal mouthwash: a double-blind, randomized clinical trial. Eur J Med Res 2023;28(1):109.
  • Saller R, Beschomer M, Hellenbrecht D, et al. Dose dependency of symptomatic relief of complaints by chamomile steam inhalation in patients with common cold. Eur J Pharmacol 1990;183:728-729.
  • Sarris J, Ravindran A, Yatham LN, et al. Clinician guidelines for the treatment of psychiatric disorders with nutraceuticals and phytoceuticals: The World Federation of Societies of Biological Psychiatry (WFSBP) and Canadian Network for Mood and Anxiety Treatments (CANMAT) Taskforce. World J Biol Psychiatry 2022;23(6):424-455.
  • Savino F, Cresi F, Castagno E, et al. A randomized double-blind placebo-controlled trial of a standardized extract of Matricariae recutita, Foeniculum vulgare and Melissa officinalis (ColiMil) in the treatment of breastfed colicky infants. Phytother Res 2005;19:335-40.
  • Segal R, Pilote L. Warfarin interaction with Matricaria chamomilla. CMAJ 2006;174:1281-2.
  • Sharifi H, Mianie MB, Qasemzadeh MG, Ataei N, Gharehbeglou M, Heydari M. Topical use of matricaria recutita L (chamomile) oil in the treatment of monosymptomatic enuresis in children: a double-blind randomized controlled trial. J Evid Based Complementary Altern Med. 2017 Jan;22(1):12-17.
  • Sharma AK, Basu I, Singh S. Efficacy and safety of Ashwagandha root extract in subclinical hypothyroid patients: a double-blind, randomized placebo-controlled trial. J Altern Complement Med. 2018 Mar;24(3):243-248.
  • Storr M, Sibaev A, Weiser D, et al. Herbal extracts modulate the amplitude and frequency of slow waves in circular smooth muscle of mouse small intestine. Digestion 2004;70:257-64.
  • Subiza J, Subiza JL, Hinojosa M, et al. Anaphylactic reaction after the ingestion of chamomile tea; a study of cross-reactivity with other composite pollens. J Allergy Clin Immunol 1989;84:353-8.
  • Subiza J, Subiza JL, Hinojosa M, et al. Anaphylactic reaction after the ingestion of chamomile tea; a study of cross-reactivity with other composite pollens. J Allergy Clin Immunol 1989;84:353-8.
  • Tavakoli Ardakani M, Ghassemi S, Mehdizadeh M, Mojab F, Salamzadeh J, Ghassemi S, Hajifathali A. Evaluating the effect of matricaria recutita and mentha piperita herbal mouthwash on management of oral mucositis in patients undergoing hematopoietic stem cell transplantation: a randomized, double blind, placebo controlled clinical trial. Complement Ther Med 2016 Dec;29:29-34.
  • van der Heijden MJE, O’Flaherty LA, van Rosmalen J, de Vos S, McCulloch M, van Dijk M. Aromatherapy massage seems effective in critically ill children: an observational before-after study. Paediatr Neonatal Pain 2022;4(2):61-68.
  • van Ketel WG. Allergy to Matricaria chamomilla. Contact Dermatitis 1982;8:143.
  • van Ketel WG. Allergy to Matricaria chamomilla. Contact Dermatitis 1987;16:50-1.
  • Viola H, Wasowski C, Levi de Stein M, et al. Apigenin, a component of Matricaria recutita flowers, is a central benzodiazepine receptors-ligand with anxiolytic effects. Planta Med 1995;61:213-6.
  • Wang Y, Tang H, Nicholson JK, et al. A metabonomic strategy for the detection of the metabolic effects of chamomile (Matricaria recutita L.) ingestion. J Agric Food Chem 2005;53:191-6.
  • Weizman Z, Alkrinawi S, Goldfarb D, et al. Efficacy of herbal tea preparation in infantile colic. J Pediatr 1993;122(4):650-652.
  • Williams AS, Dove J, Krock JE, et al. Efficacy of Inhaled Essential Oil Use on Selected Symptoms Affecting Quality of Life in Patients With Cancer Receiving Infusion Therapies. Oncol Nurs Forum 2022;49(4):349-358.
  • Zeggwagh NA, Michel JB, Eddouks M. Vascular effects of aqueous extract of Chamaemelum nobile: in vitro pharmacological studies in rats. Clin Exp Hypertens 2013;35(3):200-6.
  • Zeggwagh NA, Moufid A, Michel JB, Eddouks M. Hypotensive effect of Chamaemelum nobile aqueous extract in spontaneously hypertensive rats. Clin Exp Hypertens 2009;31(5):440-50.
  • Zick SM, Wright BD, Sen A, Arnedt JT. Preliminary examination of the efficacy and safety of a standardized chamomile extract for chronic primary insomnia: a randomized placebo-controlled pilot study. BMC Complement Altern Med 2011;11:78.

Spearmint

  • Abe, S., Maruyama, N., Hayama, K., Inouye, S., Oshima, H., and Yamaguchi, H. Suppression of neutrophil recruitment in mice by geranium essential oil. Mediators.Inflamm. 2004;13(1):21-24.
  • Abe, S., Maruyama, N., Hayama, K., Ishibashi, H., Inoue, S., Oshima, H., and Yamaguchi, H. Suppression of tumor necrosis factor-alpha-induced neutrophil adherence responses by essential oils. Mediators.Inflamm. 2003;12(6):323-328.
  • Akdogan M, Ozguner M, Aydin G, Gokalp O. Investigation of biochemical and histopathological effects of Mentha piperita Labiatae and Mentha spicata Labiatae on liver tissue in rats. Hum Exp Toxicol 2004;23:21-8.
  • Akdogan M, Ozguner M, Kocak A, et al. Effects of peppermint teas on plasma testosterone, follicle-stimulating hormone, and luteinizing hormone levels and testicular tissue in rats. Urology 2004;64:394-8.
  • Akdogan, M., Kilinc, I., Oncu, M., Karaoz, E., and Delibas, N. Investigation of biochemical and histopathological effects of Mentha piperita L. and Mentha spicata L. on kidney tissue in rats. Hum.Exp Toxicol. 2003;22(4):213-219.
  • Akdogan, M., Tamer, M. N., Cure, E., Cure, M. C., Koroglu, B. K., and Delibas, N. Effect of spearmint (Mentha spicata Labiatae) teas on androgen levels in women with hirsutism. Phytother.Res 2007;21(5):444-447.
  • Andersen, K. E. Contact allergy to toothpaste flavors. Contact Dermatitis 1978;4(4):195-198.
  • Arumugam, P. Priya N. Subathra M. Ramesh A. Environmental Toxicology & Pharmacology 2008;26(1):92-95.
  • Baker, J. R., Bezance, J. B., Zellaby, E., and Aggleton, J. P. Chewing gum can produce context-dependent effects upon memory. Appetite 2004;43(2):207-210.
  • Bardaweel SK, Bakchiche B, ALSalamat HA, Rezzoug M, Gherib A, Flamini G. Chemical composition, antioxidant, antimicrobial and antiproliferative activities of essential oil of Mentha spicata L. (Lamiaceae) from Algerian Saharan atlas. BMC Complement Altern Med. 2018;18(1):201.
  • Bonamonte, D., Mundo, L., Daddabbo, M., and Foti, C. Allergic contact dermatitis from Mentha spicata (spearmint). Contact Dermatitis 2001;45(5):298.
  • Bulat, R., Fachnie, E., Chauhan, U., Chen, Y., and Tougas, G. Lack of effect of spearmint on lower oesophageal sphincter function and acid reflux in healthy volunteers. Aliment.Pharmacol Ther. 1999;13(6):805-812.
  • Clayton, R. and Orton, D. Contact allergy to spearmint oil in a patient with oral lichen planus. Contact Dermatitis 2004;51(5-6):314-315.
  • Connelly AE, Tucker AJ, Tulk H, et al. High-rosmarinic acid spearmint tea in the management of knee osteoarthritis symptoms. J Med Food 2014;17:1361-7.
  • Dal Sacco, D., Gibelli, D., and Gallo, R. Contact allergy in the burning mouth syndrome: a retrospective study on 38 patients. Acta Derm.Venereol. 2005;85(1):63-64.
  • Damiani E, Aloia AM, Priore MG, et al. Allergy to mint (Mentha spicata). J Investig Allergol Clin Immunol 2012;22:309-10.
  • de Sousa, D. P., Farias Nobrega, F. F., and de Almeida, R. N. Influence of the chirality of (R)-(-)- and (S)-(+)-carvone in the central nervous system: a comparative study. Chirality 5-5-2007;19(4):264-268.
  • 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
  • Falcone PH, Nieman KM, Tribby AC, et al. The attention-enhancing effects of spearmint extract supplementation in healthy men and women: a randomized, double-blind, placebo-controlled, parallel trial. Nutr Res. 2019;64:24-38.
  • Falcone PH, Tribby AC, Vogel RM, et al. Efficacy of a nootropic spearmint extract on reactive agility: a randomized, double-blind, placebo-controlled, parallel trial. J Int Soc Sports Nutr. 2018;15(1):58.
  • Francalanci, S., Sertoli, A., Giorgini, S., Pigatto, P., Santucci, B., and Valsecchi, R. Multicentre study of allergic contact cheilitis from toothpastes. Contact Dermatitis 2000;43(4):216-222.
  • Goncalves, J. C., Oliveira, Fde S., Benedito, R. B., de Sousa, D. P., de Almeida, R. N., and de Araujo, D. A. Antinociceptive activity of (-)-carvone: evidence of association with decreased peripheral nerve excitability. Biol Pharm Bull. 2008;31(5):1017-1020.
  • Grant, P. Spearmint herbal tea has significant anti-androgen effects in polycystic ovarian syndrome. A randomized controlled trial. Phytother.Res 2010;24(2):186-188.
  • Gunatheesan S, Tam MM, Tate B, et al. Retrospective study of oral lichen planus and allergy to spearmint oil. Australas J Dermatol 2012;53:224-8.
  • Guney, M., Oral, B., Karahanli, N., Mungan, T., and Akdogan, M. The effect of Mentha spicata Labiatae on uterine tissue in rats. Toxicol.Ind.Health 2006;22(8):343-348.
  • Herrlinger KA, Nieman KM, Sanoshy KD, et al. Spearmint extract improves working memory in men and women with age-associated memory impairment. J Altern Complement Med. 2018;24(1):37-47.
  • Hunt R, Dienemann J, Norton HJ, Hartley W, Hudgens A, Stern T, Divine G. Aromatherapy as treatment for postoperative nausea: a randomized trial. Anesth Analg 2013;117(3):597-604.
  • Imai, H., Osawa, K., Yasuda, H., Hamashima, H., Arai, T., and Sasatsu, M. Inhibition by the essential oils of peppermint and spearmint of the growth of pathogenic bacteria. Microbios 2001;106 Suppl 1:31-39.
  • Johnson, A. J. and Miles, C. Chewing gum and context-dependent memory: the independent roles of chewing gum and mint flavour. Br.J Psychol. 2008;99(Pt 2):293-306.
  • Johnson, A. J. and Miles, C. Evidence against memorial facilitation and context-dependent memory effects through the chewing of gum. Appetite 2007;48(3):394-396.
  • Kumar, V., Kural, M. R., Pereira, B. M., and Roy, P. Spearmint induced hypothalamic oxidative stress and testicular anti-androgenicity in male rats – altered levels of gene expression, enzymes and hormones. Food Chem Toxicol. 2008;46(12):3563-3570.
  • Larsen, W., Nakayama, H., Fischer, T., Elsner, P., Frosch, P., Burrows, D., Jordan, W., Shaw, S., Wilkinson, J., Marks, J., Jr., Sugawara, M., Nethercott, M., and Nethercott, J. Fragrance contact dermatitis: a worldwide multicenter investigation (Part II). Contact Dermatitis 2001;44(6):344-346.
  • Lasrado JA, Nieman KM, Fonseca BA, et al. Safety and tolerability of a dried aqueous spearmint extract. Regul Toxicol Pharmacol 2017;86:167-176.
  • Masumoto, Y., Morinushi, T., Kawasaki, H., Ogura, T., and Takigawa, M. Effects of three principal constituents in chewing gum on electroencephalographic activity. Psychiatry Clin.Neurosci. 1999;53(1):17-23.
  • Miles, C. and Johnson, A. J. Chewing gum and context-dependent memory effects: a re-examination. Appetite 2007;48(2):154-158.
  • Ormerod, A. D. and Main, R. A. Sensitisation to “sensitive teeth” toothpaste. Contact Dermatitis 1985;13(3):192-193.
  • Poon, T. S. and Freeman, S. Cheilitis caused by contact allergy to anethole in spearmint flavoured toothpaste. Australas.J Dermatol. 2006;47(4):300-301.
  • Pratap, S, Mithravinda, Mohan, YS, Rajoshi, C, and Reddy, PM. Antimicrobial activity and bioautography of essential oils from selected Indian medicinal plants (MAPS-P-410). International Pharmaceutical Federation World Congress 2002;62:133.
  • Rafii, F. and Shahverdi, A. R. Comparison of essential oils from three plants for enhancement of antimicrobial activity of nitrofurantoin against enterobacteria. Chemotherapy 2007;53(1):21-25.
  • Rasooli, I., Shayegh, S., and Astaneh, S. The effect of Mentha spicata and Eucalyptus camaldulensis essential oils on dental biofilm. Int J Dent.Hyg. 2009;7(3):196-203.
  • Skrebova, N., Brocks, K., and Karlsmark, T. Allergic contact cheilitis from spearmint oil. Contact Dermatitis 1998;39(1):35.
  • Sokovic, M. D., Vukojevic, J., Marin, P. D., Brkic, D. D., Vajs, V., and van Griensven, L. J. Chemical composition of essential oils of Thymus and Mentha species and their antifungal activities. Molecules. 2009;14(1):238-249.
  • Soliman, K. M. and Badeaa, R. I. Effect of oil extracted from some medicinal plants on different mycotoxigenic fungi. Food Chem.Toxicol 2002;40(11):1669-1675.
  • Tomson, N., Murdoch, S., and Finch, T. M. The dangers of making mint sauce. Contact Dermatitis 2004;51(2):92-93.
  • Torney, L. K., Johnson, A. J., and Miles, C. Chewing gum and impasse-induced self-reported stress. Appetite 2009;53(3):414-417.
  • Tucha, O., Mecklinger, L., Maier, K., Hammerl, M., and Lange, K. W. Chewing gum differentially affects aspects of attention in healthy subjects. Appetite 2004;42(3):327-329.
  • Vejdani R, Shalmani HR, Mir-Fattahi M, et al. The efficacy of an herbal medicine, Carmint, on the relief of abdominal pain and bloating in patients with irritable bowel syndrome: a pilot study. Dig Dis Sci. 2006 Aug;51:1501-7.
  • Wilkinson, L., Scholey, A., and Wesnes, K. Chewing gum selectively improves aspects of memory in healthy volunteers. Appetite 2002;38(3):235-236.
  • Yu, T. W., Xu, M., and Dashwood, R. H. Antimutagenic activity of spearmint. Environ Mol.Mutagen. 2004;44(5):387-393.
  • Zhao, C. Z., Wang, Y., Tang, F. D., Zhao, X. J., Xu, Q. P., Xia, J. F., and Zhu, Y. F. [Effect of Spearmint oil on inflammation, oxidative alteration and Nrf2 expression in lung tissue of COPD rats]. Zhejiang.Da.Xue.Xue.Bao.Yi.Xue.Ban. 2008;37(4):357-363.

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 our website. 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.<

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