Active substanceAmmonium chloride + Anise common seed oil + Sodium benzoate + Sodium bicarbonate + Licorice root extract + Thermopsy lanceolate grass extractAmmonium chloride + Anise common seed oil + Sodium benzoate + Sodium bicarbonate + Licorice root extract + Thermopsy lanceolate grass extract
Dosage form: & nbspPowder for solution for oral administration
Composition:

Composition for a single dose package:

Active substances: Thermopsis extract dry - 0.045 g Licorice extract dry - 0.15 g Sodium benzoate - 0.30 g Sodium bicarbonate - 0.30 g Ammonium chloride - 0.15 g

Excipients: Essential anisic oil - 0.0037 g Sugar (refined sugar) - 0.75 g

Description:

A non-uniform powder mixture of brownish-gray color with white impregnations, with the smell of anise oil. The aqueous solution of the preparation (1:10) has a brown color.

Pharmacotherapeutic group:Expectorant of plant origin
ATX: & nbsp

R.05.C.A.10   Combination of expectorants

Pharmacodynamics:

The combined preparation has an expectorant, anti-inflammatory effect. Thermopsis dry extract enhances the secretion of the bronchial glands; Licorice extract has an anti-inflammatory, expectorant and antispasmodic effect. Sodium bicarbonate shifts the pH of bronchial mucus to the alkaline side, reduces the viscosity of sputum; the root of licorice has an anti-inflammatory and antispasmodic effect; sodium benzoate and ammonium chloride have an expectorant effect.

Indications:

As an expectorant for diseases of the respiratory tract, accompanied by a cough with hard-to-separate sputum (including tracheitis, bronchitis, bronchopneumonia).

Contraindications:

Hypersensitivity to the drug components, acute glomerulonephritis, acute pyelonephritis, pregnancy and the period of breastfeeding. Deficiency of sugar / isomaltase, intolerance to fructose, glucose-galactose malabsorption, age to 18 years.

Dosing and Administration:

Inside, adults: The contents of one packet (single dose) dissolved in 15 mL (1 tablespoon). Cooled boiled water, taken orally 3-4 times per day.

Course treatment 2-3 weeks.

Side effects:There may be allergic reactions, nausea, vomiting, diarrhea; can have irritating effect on the mucous membrane of the stomach.
Overdose:

So far, no cases of overdose have been reported.

Interaction:

It is not recommended simultaneous reception with antitussive drugs, as well as with drugs that reduce the formation of sputum.

Special instructions:

For diabetics: carbohydrate content of a single dose of the drug corresponds to 0.06 XE.

Effect on the ability to drive transp. cf. and fur:

The drug does not affect the ability to drive and engage in other potentially hazardous activities that require high concentration and rapid psychomotor reactions.

Form release / dosage:

Powder for solution for oral administration.

Packaging:

By 1.7 g sealable packages made of multilayer composite material.

By 5 or 10 Packages together with instructions for use are placed in a pack of cardboard boxes. Packages with an equal number of instructions for use are allowed to be placed in a group package.
Storage conditions:

In a dry, the dark place at a temperature of no higher than 25 ° C.

Keep out of the reach of children.

Shelf life:

2 years.

Do not use after the expiration date.

Terms of leave from pharmacies:Without recipe
Registration number:P N003614 / 01
Date of registration:09.06.2009
Expiration Date:Unlimited
The owner of the registration certificate:MOSCOW PHARMACEUTICAL FACTORY, CJSC MOSCOW PHARMACEUTICAL FACTORY, CJSC Russia
Manufacturer: & nbsp
Information update date: & nbsp08.06.2018
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