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inflammatory diseases of the lower urinary tract preventively and supportively in the treatment of patients with urolithiasis or a tendency for kidney sand to build up


Canephron is a natural preparation with a unique combination of ingredients that: relieves pain and burning, reduces bladder spasms, reduces the amount of bacteria that cause infections.
The combination of ingredients of natural origin contained in Canephron exhibits a wide spectrum of pharmacological properties: anti-inflammatory, analgesic, antispasmodic, anti-adhesive and diuretic.


Always take this medicine exactly as described in the package leaflet or as directed by your doctor. Check with your doctor or pharmacist if you are not sure.

The recommended dose is:

Adults and children over 12 years of age: orally, 3 times a day (morning, noon and evening) of 74 drops, corresponding to 5 ml in a single dose.
It is recommended to take an increased amount of fluid during use.

Canephron can be taken with other liquids (e.g. a glass of water). Shake before use. The bottle should be held upright during dosing.

Duration of treatment:

Canephron can be used for up to four weeks (for further use, after three weeks, consult your doctor). Canephron therapy can be repeated in patients who have tolerated treatment well in the past.
If the symptoms worsen or do not improve after about 7 days, then the patient should consult a doctor for further treatment.
If you take more Canephron® N than you should No cases of overdose are known. In the event of overdose, treatment should be symptomatic. It should be remembered that the preparation  contains up to 19.5% (V / V) ethanol.


100 ml of liquid contains an extract (1: 56) of 1.8 g of a mixture of Centaurium erythraea Rafn s.l., herb (thyme herb); Levisticum officinale Koch., Radix (lovage root); Rosmarinus officinalis L., folium (rosemary leaf) in a ratio (1: 1: 1).
First extrahent: 59% ethanol (V / V).
Contains up to 19.5% (V / V) of alcohol.
Excipients are: none.

Instructions For the use of medicine CANEPHRON N

Ingredients: Active ingredients: 1 tablet contains powdered medicinal plants, HerbaCentaurii 18 mg,

Radix Levistici 18 mg, Folia Rosmarini 18 mg Inactive ingredients: corn starch, silica anhydrous colloidal, lactose monohydrate, magnesium stearate, iron oxide red (E 172), riboflavin, calcium carbonate, dextrin, glucose syrup, glycol wax, castor oil, sucrose, shellac, talk, dioxide titanium.

Medication form: coated tablets. Physical and chemical properties: round orange tablets with smooth surface.

Pharmaceutical group: Urology.

Pharmaceutical properties.

Pharmacodynamics: A number of pharmacological actions are attributed to the preparation, including diuretic, spasmolytic, anti-inflammatory, ant oxidative, antibacterial, and nephroprotective effects. Canephron provides an inflammatory and diuretic effects due to the plant ingredients content.

Clinical characteristics: the treatment chronic infections of the urinary bladder (cystitis) and kidneys (pyelonephritis); noninfectious chronic inflammation of the kidneys (glomerulonephritis, interstitial nephritis); and prophylaxis against and after removal of renal stones.

Do not take CanephronN  if you have :

-hypersensitivity to active ingredients (including patients with lactose intolerance and / or fructose).

-peptic ulcer recurrence in the period.

-heart or renal failure.

Drug interaction: Unknown.  Consult healthcare provider if taking other medication.

Specific application: Immediately contact your healthcare provider if symptoms such as fever, spasms, blood in urineare present.  Before taking CanephronN consult your physician in case of sugar intolerance. It is not recommended to patients with rare forms of fructose, and lactose intolerance.

Note for diabetics: 1 tablet contains 0.02 of bread units.

Usage during pregnancy and lactation: Pregnancy: there is no negative effects of Canephron.However consult your healthcare provider before taking medication to assess individual risks.

Lactation: There is no data on effects of Canephron N during laction therefore the drug is not recommended while breastfeeding.

Usage while operating machinery or driving: No negative effects.

Usage and Dosage: Unless otherwise prescribed by doctor, adults and children over 12 years take 2 tablets 3 times a day, daily dose 6 tablets. The tablets should be swallowed without crushing. Followed by ample amount of water.  Sufficient water intake is important during treatment with Canephron N.

Duration of treatment is advised by the healthcare provider.

Children:  not recommended for children under 12 years.

Overdose: There is no reported cases of intoxication by Canephron N.  If necessary in the event of overdose of the drug symptomatic therapy is recommended.

Side effects: Mainly in patients with hypersensitivity while taking the drug Canephron N may develop allergic reactions in form of urticaria, skin rashes and itching, and redness of the skin.  In addition, in some cases, while taking the drug in patients Canephron N noted the development of vomiting, nausea and defecation disorders.

Shelf life: 4 years. Do not use the product after expiration date indicated on the package.

Storage:Store medicines in original package at room temperature. Keep medicines away from children and pets.

Packaging: 20 tablets in a blister, 3 blisters (20x3)in a box.

No prescription needed.

Manufacturer:Bionorica SE. Manufacture’s address: Kerschenstrasse 11-15, 92318 Neumarkt, Germany.



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