Tonsilgon N drops
Tonsilgon N drops
Registration code:Trade nomination of the preparation: Tonsilgon N
Drug formulation: drops for oral administration.
Composition:
Active components:
100g of Tonsilgon N drops contains 29g. of water-alcohol extract of the following kinds of medicinal herbal raw material:
althaea roots (Althaea officinalis L., Malvaceae) 0.4 g
chamomile florets (Chamornilla recutita, Asteraceae) 0.3 g
horsetail (Equisetum arvense, Equisetaceae) 0.5 g
грецкого ореха листья (Juglandis regia L, Juglandeae) 0.4 g
walnut leaves (Acahillea millefolium, Asteraceae) 0.4 g
oak cortex (Quercus robur, Fagaceae) 0.2 g
medicinal dandelion (Taraxacum officinale, Asteraceae) 0.4 g
Auxiliary components: treated water 71 g.
Ethyl content: 16.0-19.5% (volume in volume)
Description: transparent or slightly turbid liquid of yellow-brown color with distinctive chamomile smell. Light precipitation is possible in the process of the storage.
Pharmacotherapeutic group: antiseptic remedy of the vegetative origin.
Code ATX: R 02AA20
Pharmacological properties:
Pharmacological properties respond to biologically active substances, which are the part of the preparation. Tonsilgon N produces anti-inflammatory and antiseptic effect. Active components, which are the part of the preparation - chamomile, althaea and horsetail, are conductive to the increase of activity of non-specific factors of body protection. Polysaccharides, essential oils and flavonoids of chamomile, althaea and milfoil, tannins of oak cortex produce anti-inflammatory effect and are conductive to decrease of edema of the mucous membrane of the upper respiratory tract.
Indications for use:
Acute and chronic diseases of the upper respiratory tract (tonsillitis, pharyngitis, laryngitis), preventive measures of the complications at the respiratory virus infections and as the additional remedy to the therapy with the antibiotics at the bacterial infections.
Contra indications: hyper sensibility to the components of the preparation, in particular to the plants of thistle family, alcoholism. It is not recommended to apply preparation after successful anti-alcohol treatment.
Carefully: disorder of hepar function (only after the consultation with the physician).
Application during pregnancy and breast-feeding period:
The application of Tonsilgon N is possible in the period of pregnancy or breast-feeding only after the consultation with the physician.
Posology and method of administration: drops for oral administration in undiluted form, keep in oral cavity for some time before swallowing.
In acute period of the development of the disease:
Adults apply by 25 drops 5-6 times a day.
School children apply by 15 drops 5-6 times a day.
Preschool children apply by 10 drops 5-6 times a day.
Breastfed children apply by 5 drops 5-6 times a day.
It is necessary to continue the treatment with Tonsilgon N during 1 week after the disappearing of the acuteness of the disease.
After the disappearing of the acute symptoms:
Adults apply by 25 drops 3 times a day.
School children apply 15 drops 3 times a day.
Preschool children apply 10 drops 3 times a day.
Breastfed children apply 5 drops 3 times a day.
Side effects: allergic response is possible.
Overdosage: there are no any restrictions in the application of this medicine up to the present time at the application according to recommended regime.
Interaction with other medication:
The combination with antibacterial medicine is possible. The interaction with other medicine is not found up to the present time.
Special remarks:
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 does not decrease the ability to drive a car of work with mechanisms if application is in the recommended dosage.
Form of issue: drops for oral administration, drops are 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: 2 years. Do not use preparation if the expiry date (month and year) printed on the pack has passed.
Pharmacy purchasing terms: Without receipt.
Manufacturing enterprise:
BIONORIKA AG D-92318 Neumarkt/Germany
Kerschenstaistrasse 11-15
92318 Neumarkt
Germany
Representative office in Moscow
119 526, Moscow, Vernadski prospect, house 105, building 2
phone. 502-90-19.