Active substanceSalicylic acidSalicylic acid
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  • Dosage form: & nbspSolution for external use alcohol.
    Composition:
    Active substance: salicylic acid - 10 g, 20 g
    Excipient: Ethanol (ethyl alcohol) 70% to 1 L

    Description:Colorless transparent liquid with the smell of alcohol.
    Pharmacotherapeutic group:Keratolytic agent.
    ATX: & nbsp

    D.01.A.E   Other antifungal agents for external use

    D.01.A.E.12   Salicylic acid

    Pharmacodynamics:
    Means for external use. Has keratolytic, antiseptic, local irritating and anti-inflammatory effect. Promotes softening and peeling of the cornified epithelium.

    Pharmacokinetics:Not studied.
    Indications:Greasy seborrhea, chronic eczema, acne vulgaris.
    Contraindications:Hypersensitivity to the components of the drug, kidney failure, infantile age.
    Pregnancy and lactation:
    After consulting a doctor, the drug may be administered according to the instructions if the expected benefit to the mother exceeds the potential risk to the fetus and the baby.

    Dosing and Administration:
    Outwardly.The drug is applied to the affected surface 2-3 times a day. The maximum daily dose for adults is 20 ml (for 1% solution) or 10 ml (for 2% solution). The course of treatment - no more than 1 week.

    Side effects:Possible individual intolerance, allergic reactions, incl. local (burning, itching, skin hyperemia).
    Overdose:No data available.
    Interaction:Salicylic acid can increase skin permeability for other medicaments for topical use and thereby enhance their absorption. Sucked up salicylic acid can increase the side effects of methotrexate and oral hypoglycemic JIC, sulfonylurea derivatives. A solution of salicylic acid is incompatible with resorcinol (melted mixture is formed) and zinc oxide (zinc salicylate insoluble).
    Special instructions:
    When treating children, several areas of the skin should be avoided at the same time. In case of contact with mucous membranes, rinse the area with a large amount of water; Do not use in the eye area, do not apply to mucous membranes.

    Effect on the ability to drive transp. cf. and fur:The use of the drug in accordance with the instructions does not affect the management of motor vehicles and the employment of other potentially hazardous activities requiring increased concentration of attention and speed of psychomotor reactions.
    Form release / dosage:
    Solution for external use alcohol 1%, 2%.


    Packaging:
    For 40 ml in bottles of orange glass with a screw neck type PV. Vials with equal number of instructions for use are placed in a group package.

    Storage conditions:
    In a dark place at a temperature of no higher than 25 ° C. Keep out of the reach of children.

    Shelf life:
    3 years. Do not use after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:P N003081 / 01
    Date of registration:02.10.2009
    The owner of the registration certificate:YAROSLAVSK PHARMACEUTICAL FACTORY, CJSC YAROSLAVSK PHARMACEUTICAL FACTORY, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp14.08.2015
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