Active substanceAlthea Medicinal Roots Extract + Ammonium Chloride + Anise Ordinary Seed Oil + Sodium Benzoate + Sodium Hydrocarbonate + Licorice Root ExtractAlthea Medicinal Roots Extract + Ammonium Chloride + Anise Ordinary Seed Oil + Sodium Benzoate + Sodium Hydrocarbonate + Licorice Root Extract
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  • Cough medicine for children dry
    powder inwards d / children 
  • Cough medicine for children dry
    powder d / children inwards 
    LYUMI, LLC     Russia
  • Cough medicine for children dry
    powder inwards d / children 
  • Dosage form: & nbsppowder for solution for oral administration [for children]
    Composition:

    Active substances: althea roots extract dry - 0.300 g; licorice roots extract dry - 0,075 g; sodium benzoate - 0.150 g; sodium bicarbonate 0.150 g; ammonium chloride -0,0375 g

    Excipients: anise oil - 0.0037 g; sucrose to 1.47 g
    Description:Inhomogeneous powder brownish-gray color with lighter inclusions, 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.F.B.02   Antitussive drugs in combination with expectorants

    R.05.F   Antitussive drugs in combination with expectorants

    Pharmacodynamics:The combined preparation has an expectorant, anti-inflammatory effect. Althea roots 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:AT as an expectorant for diseases of the respiratory tract, accompanied by a cough with hard-to-recover sputum (including tracheitis, bronchitis, bronchopneumonia).
    Contraindications:Hypersensitivity to the drug components, acute glomerulonephritis, acute pyelonephritis, pregnancy, the period of breastfeeding. Deficiency of sugar / isolematase, intolerance to fructose, glucose-galactose malabsorption.
    Dosing and Administration:Inside, for children: dissolve the contents of 1 packet in 15 ml (1 tablespoon) of cooled boiled water.Take 3-4 times a day after meals: children under 1 year - 15-25 drops; children 1-2 years - 40 drops each; children 3-4 years old ½ a teaspoonful (2.5 ml); children 5-6 years old 3/4 a teaspoonful (3.75 ml); children 7-8 years - 1 teaspoonful (5ml); children 9-12 years - 2 teaspoons (10 ml); children over 12 years - 1 tablespoon (15 ml). The course of treatment is 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.

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

    The drug has no effect on the ability to perform potentially hazardous activities requiring increased concentration of attention and speed of psychomotor reactions (including driving, working with moving mechanisms).

    Form release / dosage:

    Powder for solution for oral administration [for children].

    Packaging:

    For 1.47 grams in heat-sealed bags.

    Packages are placed in a group package with an equal number of instructions for use.
    Storage conditions:

    In a dry place at a temperature of no higher than 25 ° C. Keep out of the reach of children.

    Shelf life:

    Shelf life. 1,5 years. Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:PL-000999
    Date of registration:18.10.2011 / 11.09.2012
    Expiration Date:Unlimited
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Information update date: & nbsp08.06.2018
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