Our signature product
Urinary Tract SupporTea
$9.99 – $26.99
You’re ready to try something new when it comes to your urinary tract health. We’ve been there. That’s where this doctor recommended tea comes in. It’s worked for our founder, worked for our customers, and now it can work for you in 48 hours too.
What sets Nuna Med’s SupporTea apart:
- 80% of users experience improvement following onset*
- Compostable, non-GMO tea sachets
- Can be used as a 48 hour “Onset” option (4 sachets in first 24hrs + 4 sachets in second 24hrs = 8 bags of tea in 48hrs) or for “Avoidance”
- Herbs thoroughly tested by 3rd party labs during all phases of the production process
- Soothing, herbal tea taste and smell
- Produced in compliance with Good Manufacturing Practices (GMPs)
- Made in the USA using domestic and imported organic and wildcrafted ingredients
*80.95% determined using data collected over the past 8 years from patients who have used this proprietary blend
NOTE: our 8 count signature tin is currently SOLD OUT! If you are looking for an 8 count, please add the 8 count pouch to your cart. We should have tins back in stock shortly. Thank you for your patience!
Q & A
What is the maximum amount someone should consume Urinary Tract SupporTea per month?
How will I know the tea is working?
Is there anything I can do to make the product more effective?
What does a kidney infection feel like?
Can I use Urinary Tract SupporTea while pregnant?
Can it be taken when women are breastfeeding?
Can it be taken by people with Diabetes, Type I or II?
Can it be taken by people with transplants (e.g. kidney)?
What is Urinary Tract SupporTea’s shelf life?
Does the tea have to be warm/hot each time I consume it? Or can it be iced or room temperature?
Latin name: Arctostaphylos uva-ursi
Other names: bearberry, kinnickinick
“The prophylactic effect of UVA-E on recurrent cystitis was evaluated in a double-blind, prospective, randomized study. A total of 57 women who had suffered at least three episodes of cystitis during the year preceding the study were treated with either UVA-E (n = 30) or placebo (n = 27) for 1 month. At the end of the 1-year follow-up period, a statistically significant difference between groups in the number of recurrences was seen. No side effects were reported. We conclude that UVA-E exerts a prophylactic effect on recurrent cystitis.”
“Uva-ursi folium (bearberry leaf) has been traditionally used to treat symptoms of lower urinary tract infections. The most representative constituent of this herbal drug is arbutin that is rapidly absorbed in the small intestine and undergoes hepatic conjugation to form hydroquinone (HQ) conjugates. As free HQ is crucial for the safety of the herbal preparation, we reviewed published and unpublished experimental and human studies to clarify some outdated assumptions and to support the safety of therapeutic daily doses of Uva-ursi folium extract. Specifically, data on pharmacokinetics and the human exposure of arbutin and HQ were reviewed.
A therapeutic recommended human daily dose of bearberry leaf extract (420 mg hydroquinone derivatives calculated as anhydrous arbutin) liberates free HQ in urine at a maximum exposure level of 11 µg/kg body weight (bw)/d. By means of an experimental no observed effect level value, a permitted daily exposure dose below which there is a negligible risk to human health was estimated for free HQ (100 µg/kg bw/d). Dietary sources of arbutin/HQ that are regularly consumed long term by humans generate comparable free HQ exposure levels.
There is no direct evidence, regarding human data, supporting the fact that free HQ causes convulsion, hepatotoxicity, nephrotoxicity, or promotion of tumors in humans. Free HQ had no activity promoting pancreatic, bladder, stomach, or liver carcinogenesis. In conclusion, under the recommended use conditions Uva-ursi folium is a safe therapeutic option for treating lower urinary tract infections.”
de Arriba, S. G., Naser, B., & Nolte, K. U. (2013). Risk assessment of free hydroquinone derived from Arctostaphylos Uva-ursi folium herbal preparations. International journal of toxicology, 32(6), 442-453.
Beaux, D., Fleurentin, J., & Mortier, F. (1999). Effect of extracts of Orthosiphon stamineus benth, Hieracium pilosella L., Sambucus nigra L. and Arctostaphylos uva‐ursi (L.) spreng. in rats. Phytotherapy Research, 13(3), 222-225.
Chauhan, B., Yu, C., Krantis, A., Scott, I., Arnason, J. T., Marles, R. J., & Foster, B. C. (2007). In vitro activity of uva-ursi against cytochrome P450 isoenzymes and P-glycoprotein. Canadian journal of physiology and pharmacology, 85(11), 1099-1107.
Koehler, J., & Franz, G. (1993). Bioavailability of drug preparations containing a leaf extract of Arctostaphylos uva-ursi (L.) Sprengl.(Uvae ursi folium). Pharmaceutical and pharmacological letters, 3, 63-66.
Kubo, M., Ito, M., Nakata, H., & Matsuda, H. (1990). Pharmacological studies on leaf of Arctostaphylos uva-ursi (L.) Spreng. I. Combined effect of 50% methanolic extract from Arctostaphylos uva-ursi (L.) Spreng.(bearberry leaf) and prednisolone on immuno-inflammation. Yakugaku zasshi: Journal of the Pharmaceutical Society of Japan, 110(1), 59-67.
Matsuda, H., Nakamura, S., Shiomoto, H., Tanaka, T., & Kubo, M. (1992). Pharmacological studies on leaf of Arctostaphylos uva-ursi (L.) Spreng. IV. Effect of 50% methanolic extract from Arctostaphylos uva-ursi (L.) Spreng.(bearberry leaf) on melanin synthesis. Yakugaku zasshi: Journal of the Pharmaceutical Society of Japan, 112(4), 276-282.
Matsuda, H., Tanaka, T., & Kubo, M. (1991). Pharmacological studies on leaf of Arctostaphylos uva-ursi (L.) Spreng. III. Combined effect of arbutin and indomethacin on immuno-inflammation. Yakugaku zasshi: Journal of the Pharmaceutical Society of Japan, 111(4-5), 253-258.
Shimizu, M., Shiota, S., Mizushima, T., Ito, H., Hatano, T., Yoshida, T., & Tsuchiya, T. (2001). Marked potentiation of activity of β-lactams against methicillin-resistant Staphylococcus aureus by corilagin. Antimicrobial agents and chemotherapy, 45(11), 3198-3201.
Latin name: Chimaphilla umbellata
Other names: prince’s pine, king’s cure, ground holly, love in winter, rheumatism weed, umbellate wintergreen
Galván, et al. notes that “Chimaphila umbellata (L.) W. Bart (Pyrolaceae), commonly known as pipsissewa or umbellate wintergreen, has been used by First Nations Peoples of eastern Canada as a traditional medicine for infections, inflammations of various kinds, kidney stones, gonorrhea, stomachache, backache, and coughs; it has also been used as a blood purifier, diuretic and astringent.”
Galván, I. J., Mir-Rashed, N., Jessulat, M., Atanya, M., Golshani, A., Durst, T., … & Cruz, I. (2008). Antifungal and antioxidant activities of the phytomedicine pipsissewa, Chimaphila umbellata. Phytochemistry, 69(3), 738-746.
Kedzia, B., Wrociński, T., Mrugasiewicz, K., Gorecki, P., & Grzewińska, H. (1975). Antibacterial action of urine containing products of arbutin metabolism. Medycyna doswiadczalna i mikrobiologia, 27(3), 305-314.
Schindler, G., Patzak, U., Brinkhaus, B., Nieciecki, A., Wittig, J., Krähmer, N., … & Veit, M. (2002). Urinary Excretion and Metabolism of Arbutin after Oral Administration of Arctostaphylos uvae ursi Extract as Film‐Coated Tablets and Aqueous Solution in Healthy Humans. The Journal of Clinical Pharmacology, 42(8), 920-927.
Shin, B. K., Kim, J., Kang, K. S., Piao, H. S., Park, J. H., & Hwang, G. S. (2015). A new naphthalene glycoside from Chimaphila umbellata inhibits the RANKL-stimulated osteoclast differentiation. Archives of pharmacal research, 38(11), 2059-2065.
Latin name: Plantago lanceolata
Other names: broad-leaf plantain, greater plantain
Dalar el al. concluded that “Aqueous extracts of Plantago lanceolata and Malva neglecta, two plants from eastern regions of Turkey used as medicinal plants, exhibited potent antioxidant capacities, comparable or superior to multiple herbs and Chinese medicinal plants. The levels of phenolic compounds correlated well with antioxidant activities.”
Dalar, A., Türker, M., & Konczak, I. (2012). Antioxidant capacity and phenolic constituents of Malva neglecta Wallr. and Plantago lanceolata L. from Eastern Anatolia Region of Turkey. Journal of Herbal Medicine, 2(2), 42-51.
Kalantari, A., Kósa, D., Nemes, D., Ujhelyi, Z., Fehér, P., Vecsernyés, M., … & Vasas, G. (2017). Self-Nanoemulsifying Drug Delivery Systems Containing Plantago lanceolata—An Assessment of Their Antioxidant and Antiinflammatory Effects. Molecules, 22(10), 1773.
Latin name: Agathosma betulina
Other names: round buchu, short buchu
“Buchu leaves and oil of buchu were used by the indigenous people of South Africa for hundreds of years. The medicinal use of buchu was taken up by the early Dutch settlers and later introduced into the pharmaceutical industry in the UK.
Buchu preparations are now used as a diuretic and for a wide range of conditions including stomach aches, rheumatism, bladder and kidney infections and coughs and colds.”
“Biosynthesis of certain compounds in in vitro culture of Buchu was induced by plant growth regulator application compared to the control. The plants possess a number of pharmacological properties including anticancer, antimicrobial and antioxidant.”
Latin name: Urtica dioica
Other names: stinging nettle
Notes that “In urinary conditions, stinging nettle herb is used for reducing hematuria due to infection or stones, increasing volume of urine, and for reducing kidney stone size or recurrence.”
A review of Safarinejad’s study highlights that, “Results [from Safarinejad’s study] offer some preliminary evidence that long-term treatment (up to 18 months) with stinging nettle root might substantially improve lower urinary tract symptoms in men with BPH [benign prostatic hyperplasia]. The degree of improvement is impressive, with an 8 point improvement in the IPSS in 6 months, compared to a 1.5 point improvement with placebo.”
Safarinejad, M. R. (2005). Urtica dioica for treatment of benign prostatic hyperplasia: a prospective, randomized, double-blind, placebo-controlled, crossover study. Journal of herbal pharmacotherapy, 5(4), 1-11.
Latin name: Althaea officinalis
Other names: althaea, althea
“The hexane extracts of flower and root of Althaea officinalis which were collected from northwestern Iran (Khalkhal) were obtained by Soxhlet apparatus. The fatty acids were derived from methyl esters and determined by gas chromatography/flame ionization detector (GC/FID) and gas chromatograph/mass spectrometry (GC/MS) systems. The hexane extract from the flower and root contained omega-3 (20.5 and 14.9%, respectively). The other main compounds of the flower extract were palmitic acid (13.0%), heptacosane (9.3%) and nonacosane (11.2%).
In the root extract, palmitic acid (16.8%), linoleic acid (omega-6) (28.0%) and naphthalene decahydro 2, 6- dimethyl (16.4%) were the main components. The antimicrobial activity of the hexane extracts of those samples were determined against some Gram-positive and Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Bacillus subtilis, Enterococcus faecalis, Staphylococcus aureus and Staphylococcus epidermidis), as well as three fungi (Aspergillus niger, Candida albicans and Saccharomyces cerevisiae). The bioassay showed that the both extracts exhibited good antimicrobial activity. This study reveals that all the parts of this plant are attractive sources of fatty acid components.”
Valiei, M., Shafaghat, A., & Salimi, F. (2011). Chemical composition and antimicrobial activity of the flower and root hexane extracts of Althaea officinalis in Northwest Iran. Journal of Medicinal Plants Research, 5(32), 6972-6976.
Other Urinary Tract Herbs and Literature
Rotblatt, M., & Ziment, I. (Eds.). (2002). Evidence-based herbal medicine. Hanley & Belfus.