Salicylic ointment (Salicylic oinment)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceSalicylic acidSalicylic acid
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    • Dosage form: & nbsp
    Ointment for external use.

    Composition:
    Active substance: Salicylic acid - 2 g or 5 g
    Excipient: Vaseline - up to 100 g

    Description:Homogeneous mass from white to light yellow color.
    Pharmacotherapeutic group:keratolytic agent.
    ATX: & nbsp

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

    D.01.A.E.12   Salicylic acid

    Pharmacodynamics:Has keratolytic, antiseptic, local irritating and anti-inflammatory effect.
    Indications:Inflammatory and infectious skin lesions, burns, psoriasis, oily seborrhea, eczema, pityriasis, dyskeratosis, ichthyosis.
    Contraindications:Hypersensitivity to the components of the drug, kidney failure, childhood, pregnancy and the period of breastfeeding.
    Dosing and Administration:Apply to the affected area (about 0.2 g per 1 sq. Cm.) And cover with a sterile tissue or impose a sterile dressing impregnated with ointment (before application, the surface is cleaned of necrotic tissues, the blisters are opened, washed with antiseptic solution).Change dressings produced 1 time in 2-3 days until complete cleansing from purulent necrotic masses.
    Side effects:Local allergic reactions (burning, itching, hyperemia).
    Overdose:No data.
    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 drugs, derivatives of sulfonylurea.
    Special instructions:
    Do not apply the drug to birthmarks, hairy warts. It should be borne in mind that in cases of skin diseases that occur with hyperemia and inflammation (including psoriatic erythroderma) or with superficial dying lesions, salicylate may be absorbed. In case of contact with mucous membranes, rinse the area with plenty of water.

    Effect on the ability to drive transp. cf. and fur:The drug does not affect the ability to drive vehicles, mechanisms.
    Form release / dosage:
    Ointment for external use 2% and 5%.
    Packaging:By 25 g in a dark glass jar with a triangular aureole with lids that are stretched polymer.
    25g and 50g in aluminum tubes with polyethylene caps.
    Each jar or tube together with the instruction for use is placed in a pack of cardboard.
    It is allowed to lay cans or tubes together with an equal number of instructions for use in a group package made of cardboard.
    Storage conditions:In the dark place at a temperature of 8 to 15 ° 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:LP-001223
    Date of registration:16.11.2011
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Representation: & nbspTULA PHARMACEUTICAL FACTORY, LTD.TULA PHARMACEUTICAL FACTORY, LTD.
    Information update date: & nbsp12.08.2015
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