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Active ingredients
Homeopathic composition
Release form
Dragee
Composition
Althea roots 8 mg, chamomile flowers 6 mg; horsetail grass 10 mg; walnut leaves 12 mg; yarrow grass 4 mg; oak bark 4 mg; herb dandelion 4 mg; Auxiliary substances: lactose - 51.523 mg, maize starch - 23.29 mg , potato starch - 5.858 mg, stearic acid - 2.6 mg, dextrose (glucose) monohydrate - 0.929 mg, silicon dioxide highly dispersed - 0.65 mg.; Composition; covers: calcium carbonate - 4.339 mg, glucose syrup - 1.536 mg, indigotin - 0.002 mg, maize starch - 1.24 mg, modified maize starch - 3.785 mg, montan glycol wax - 0.13 mg, poly (1-vinyl-2-pyrrolidone) K25 - 0.112 mg, poly (1-vinyl-2-pyrrolidone) K30 - 0.246 mg, castor oil - 0.057 mg, sucrose - 62.198 mg, shellac - 1.476 mg, talc - 52.687 mg, silicon dioxide highly dispersed - 0.65 mg, titanium dioxide - 1.206 mg.
Pharmacological effect
Antiseptic agent of plant origin. Pharmacological properties due to biologically active substances that are part of the drug. Tonsilgon; H has anti-inflammatory and antiseptic effects .; The active ingredients in the composition of the drug chamomile, althea and horsetail contribute to the activity of nonspecific defense factors of the body. Polysaccharides, essential oils and flavonoids of chamomile, althea and yarrow, oak bark tannins have an anti-inflammatory effect and help reduce the swelling of the mucous membrane of the respiratory tract.
Indications
- acute and chronic diseases of the upper respiratory tract (tonsillitis, pharyngitis, laryngitis); - prevention of complications of respiratory viral infections and as an adjunct to antibiotic therapy for bacterial infections.
Contraindications
- a rare hereditary form of lactose intolerance, fructose intolerance, lactase deficiency, glucose-galactose malabsorption or sucrase-isomaltase deficiency (due to the content of lactose and sucrose in the preparation); - children's age up to 6 years; - Hypersensitivity to the drug components, in particular, to the plants of the Compositae family.
Use during pregnancy and lactation
Use of the drug during pregnancy and lactation (breastfeeding) is possible if the potential benefit to the mother outweighs the potential risk to the fetus and child. Consultation with a doctor is required.
Dosage and administration
The drug is taken orally.Drops are swallowed whole, not chewed, squeezed with water if necessary .; In the acute period of the development of the disease in adults - 2 pills 5-6 times per day, children of school age (over 6 years old) - 1 tablet 5-6 times per day; After the disappearance of the acute symptoms of the disease (sore throat), treatment with the drug should be continued for another 1 week; adults - 2 pills 3 times / day, children of school age (over 6 years old) - 1 tablet 3 times / day.
Side effects
On the part of the digestive tract: nausea, vomiting .; Allergic reactions are possible. If there are signs of an allergic reaction, you should stop taking the drug.
Overdose
To date, overdose cases have not been reported .; Symptoms: possible increased side effects of the gastrointestinal tract .; Treatment: symptomatic.
Interaction with other drugs
Combination with antibacterial drugs is possible and appropriate .; Interaction with other drugs is not described.
special instructions
If, when using the drug for 7 days, the symptoms of the disease persist or the patient's condition worsens, you should consult a doctor. One dragee contains less than 0.03 bread units counted .; Impact on the ability to drive vehicles and control mechanisms; The use of the drug does not affect the ability to perform potentially hazardous activities that require increased concentration of attention and speed of psychomotor reactions.