Active substanceZinc oxideZinc oxide
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  • Dosage form: & nbspFROMfor external use.
    Composition:

    Per 100 g:

    Active substance: zinc oxide - 12.5 g;

    Excipients: talc - 12.5 g, potato starch - 12.5 g, glycerol - 20.0 g, ethanol 70% - 20.0 g, purified water - up to 100.0 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:

    Antiseptic, astringent, drying agent. Reduces exudation and mocclusion, which removes local inflammation and irritation.

    The symptomatic effect of the drug is determined by zinc oxide.

    Indications:

    Dermatitis, skin ulcers, intertrigo.

    If necessary, please consult with your doctor before using the medication.

    Contraindications:

    Hypersensitivity to the components of the drug.

    Pregnancy and lactation:

    Possible use during pregnancy and during breastfeeding.

    Dosing and Administration:

    Outwardly. Shake before use.

    A tampon moistened with the drug, put a suspension on the affected skin 2-3 times a day.

    If there is no improvement after treatment or new symptoms appear, you should consult your doctor.

    Use the drug only according to the method of administration and the doses specified in the instructions.

    If necessary, please consult with your doctor before using the medication.

    Side effects:

    Possible local allergic reactions: itching, hyperemia, rash.

    If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.

    Overdose:

    Cases of overdose with external application are not described.

    Interaction:

    Not studied.

    Special instructions:

    Avoid contact with eyes.

    Read the instructions carefully before using the product. Keep the manual, it may be needed again. If you have any questions, contact your doctor.

    The medicinal product that you are being treated is intended for you personally, and it should not be transferred to others, as it can cause harm even if you have the same symptoms as you.

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

    The use of the drug does not affect the performance of potentially hazardous activities,requiring special attention and quick reactions (transport management, work with moving mechanisms).

    Form release / dosage:

    Suspension for external use, 12.5%.

    Packaging:

    100 g and 125 g in glass bottles with a screw neck for medicines, sealed with plastic caps and caps screwed on or in plastic bottles with a screw neck of low pressure polyethylene, sealed with a polyethylene threaded cap made of low pressure polyethylene.

    Each vial with the instruction for medical use is placed in a pack of cardboard box A or chrome-ersatz.

    It is allowed to pack 100 g and 125 g bottles into boxes with 12, 25, 40, 50 pieces of cardboard corrugated or corrugated boards with an equal number of instructions for use (for hospitals).

    Storage conditions:

    Store in a 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 the product after the expiration date printed on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-003792
    Date of registration:17.08.2016
    Expiration Date:17.08.2021
    The owner of the registration certificate:YUZHFARM, LLC YUZHFARM, LLC Russia
    Manufacturer: & nbsp
    Representation: & nbspYUZHFARM, LLCYUZHFARM, LLC
    Information update date: & nbsp09.10.2016
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