Canephron N liquid

Canephron N liquid

Registration code:
Trade nomination of the preparation: Canephron N
Drug formulation: liquid for oral administration.

100g. of Canephron N liquid contains 29g. of water-ethanol extract of the following kinds of herbal raw material:
centaury herb (Centaurium urnbellatum, Gentianaceae) 0.6 g
lovage root (Levisticum officinale, Apiaceae) 0.6 g
rosemary leaves (Rosmarinus officinale, Lamiaceae) 0.6g
Ethyl alcohol: 16.01-19.5% (volume in volume)
Additional ingredient: treated water.

Description: transparent or slightly muddy liquid of yellow-brown color with aromatic smell. The deposition during storage is possible.

Pharmacological properties: combined preparation of the vegetative origin, it produces cholagogic, spasmolytic, anti-inflammatory, antimicrobic effect.

Indications for use:
preparation is applied at the complex therapy at the treatment of chronic infections of urinary bladder (cystitis) and kidney (puelonephritis), at non-infectious chronic kidney inflammation (glomerulonephritis, interstitial nephritis), as a remedy, which prevents the formation of uroliths (and also after elimination of uroliths).

Contra indications: hyper sensibility to the components of the preparation, alcoholism. Patients after the successful anti-alcohol treatment shouldn't apply this preparation.
Carefully: hepar diseases (the application of the preparation is possible only after consultation with the physician).

Application at pregnancy and during breast-feeding period: the application of Canephron N during pregnancy or breast-feeding period is possible only after the consultation with the physician.

Posology and method of administration: apply orally, dissolving with water.
Adults: by 50 drops 3 times a day.
School-aged children: by 25 drops 3 times a day
Preschool children: by 15 drops 3 times a day
Baby at breast: by 10 drops 3 times a day
It is necessary to continue the treatment with Canephron N during 2-4 weeks after the weakening of the acuteness of the disease.
It is possible to apply drops with other liquid in order to soften the bitter taste of preparation.

Side effects: allergic response is possible.

Overdosage: the information about overdosage and intoxication is not found up to the present time.

Interaction with other medicine:
The combination with antibacterial medicine is possible and efficient. The interaction with other medicine is not found up to the present time.

Special remarks:
It is recommended to drink great amount of water after the application of the preparation. The bottle is ought to storage in the vertical position after application. Light turbidity or deposition of sediment is possible during the process of storage, which does not influence on the effectiveness of the preparation. Shake before application!
The preparation contains ethanol 16.0-19.5% (volume in volume). The preparation does not decrease the ability to drive a car of work with mechanisms if application is in the recommended dosage.

Form of issue: liquid for oral administration, in bottles of dark glass by 50 and 100 ml. with measuring device by drop infusion, with screw lid with resistance ring and dose-measuring cup on the top, it is placed into fold cardboard pack together with prescription.

Storage conditions: keep in dry and shadowed place, at temperature up to 25оС; keep away from children.

Expire date: 3 years. Do not use preparation if the expiry date (month and year) printed on the pack has passed.
Open bottles are possible to apply during 6 months.

Pharmacy purchasing terms: Without receipt.

Manufacturing enterprise:
BIONORIKA AG D-92318 Neumarkt/Germany
Kerschenstaistrasse 11-15
92318 Neumarkt 

Representative office in Moscow
119 526, Moscow, Vernadski prospect, house 105, building 2
phone. 502-90-19.

Back to the list