Active substanceZinc oxideZinc oxide
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  • Dosage form: & nbsp

    suspension for external use.

    Composition:

    Composition per 100 g of suspension:

    Zinc oxide (zinc oxide) 12.5 g, talc 12.5 g, potato starch 12.5 g, glycerol (glycerol) 20 g, ethyl alcohol 70% (ethanol) 20 g, water purified to 100 g.

    Description:Inhomogeneous suspension with a rapidly precipitated white or white precipitate after shaking, with a grayish hue of color.
    Pharmacotherapeutic group:Dermatoprotective agent.
    ATX: & nbsp

    A.12.C.B   Zinc Preparations

    Pharmacodynamics:

    Has antiseptic, astringent, drying effect.

    Indications:

    Dermatitis, skin ulcers, intertrigo.

    Contraindications:Hypersensitivity to the components of the drug.
    Dosing and Administration:

    Outwardly. Apply to the affected skin with a swab moistened with the drug, 2-3 times a day.

    Side effects:

    Local allergic reactions in the form of itching, hyperemia, rash.

    Special instructions:Possible use during pregnancy and lactation. Do not allow the drug to enter the eyes, on the wounds.
    Form release / dosage:

    Suspension for external use.

    Packaging:

    For 125 g in bottles of orange glass, placed in cardboard packs or without a pack with instructions for the use of the drug.

    Storage conditions:

    At a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years. Do not use the product after the expiration date printed on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:P N002650 / 01
    Date of registration:07.04.2009
    The owner of the registration certificate:YAROSLAVSK PHARMACEUTICAL FACTORY, CJSC YAROSLAVSK PHARMACEUTICAL FACTORY, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp09.10.2015
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