Active substanceDexpanthenolDexpanthenol
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  • Dosage form: & nbspaerosol for external use
    Composition:

    Active substance: active substance: dexpanenthenol 2.5 g or 5.0 g;

    Excipients: cetostearyl alcohol type A emulsifying, macrogolglycerol cocoate, methylparahydroxybenzoate, propylene glycol, potassium phosphate monosubstituted (potassium dihydrogen phosphate), sodium phosphate disubstituted 12-water (disodium hydrogenphosphate 12-water), purified water, chladone 134a.

    Description:

    When leaving the container, it forms white foam, with a weak specific odor.

    Pharmacotherapeutic group:tissue repair stimulant
    ATX: & nbsp

    D.03.A.X.03   Dexpanthenol

    S.01.X.A.12   Dexpanthenol

    D.03.A.X   Other drugs that promote normal scarring

    S.01.X.A   Other drugs for the treatment of eye diseases

    Pharmacodynamics:

    It has a regenerating, metabolic and weak anti-inflammatory effect. Dexpanthenol in the body forms an active metabolite - pantothenic acid, which is an integral part of coenzyme A, which catalyzes acetylation in the body, participates in virtually all metabolic processes (the cycle of tricarboxylic acids, the metabolism of carbohydrates, fats and fatty acids, phospholipids, proteins, etc.) corticosteroids, acetylation of choline.Stimulates regeneration of the skin, mucous membranes, accelerates mitosis and increases the strength of collagen fibers.

    Pharmacokinetics:

    With external application dexpanthenol quickly absorbed by the skin, turning into pantothenic acid. Especially well penetrates into the affected tissue. Pantothenic acid binds to plasma proteins (mainly with beta-globulin and albumin).

    Indications:

    - Dry skin;

    - wounds and burns (solar and thermal);

    - dermatitis; pressure sores; intertrigo; abscesses; furuncles after opening and sanitation; aseptic postoperative wounds; poorly engrafted skin grafts;

    - treatment and prevention of cracks and inflammation of the nipples of the breast during lactation;

    - nursing of infants: prevention and treatment of diaper rash in infants; activation of the healing process of the skin for minor lesions, erythema from diapers.
    Contraindications:

    Increased individual sensitivity to the components of the drug.

    Purulent wounds with heavy exudation.

    Pregnancy and lactation:

    During pregnancy and lactation, it is possible to use the drug according to the indications.

    Dosing and Administration:

    Outwardly.One or several times a day by spraying from a distance of 10-20 cm so that the damaged surface is covered with the drug. The duration of treatment depends on the severity of the disease. The course of treatment, depending on the type of pathology, can range from 2-3 days to 3-4 weeks.

    With sunburn and dermatological diseases Foam is rubbed lightly into the affected surface until the drug is absorbed into the skin. The drug is used 3-4 times a day.

    In the treatment of granulating burns, wounds and trophic ulcers with weak exudation before the application of the preparation, the wound surface is cleaned from exudate and necrotic tissues, washed with a solution of hydrogen peroxide 3%, furacilin 1: 5000 or chlorhexidine bigluconate 0.05% and dried. The foam is applied uniformly with a thickness of 1.0-1.5 cm so that the entire affected area is covered with foam and a sterile gauze bandage is applied. Change dressings are carried out 1 time in 1-2 days for the treatment of burns and 1 time per day in the treatment of wounds and trophic ulcers. With the open method of treating burns, the foam is applied 1-2 times a day. The duration of treatment is determined by the dynamics of epithelialization of wounds.

    For prevention of radiation complications in patients exposed to radiation, the drug is rubbed into the irradiated surface and skin around 3-4 times a day after irradiation during the course of irradiation, and also within 10-14 days after its termination.

    Breast Care for Nursing Mothers

    Aerosol is applied to the nipples of nursing mothers after each feeding and rubbed with massage movements.

    Babysitting

    Aerosol is applied at each change of a diaper / diaper (diaper).

    Side effects:

    In rare cases, skin allergic reactions are possible, at the appearance of which it is necessary to stop the use of the drug.

    Interaction:

    Not described.

    Special instructions:

    When using the product for the first time, shake the container thoroughly, release the first portion before the foam appears and then apply the drug to the affected area.

    Avoid contact with foam in the eyes. In case of accidental contact, the eyes should be rinsed with water.

    The drug should not be applied to wounds, burns, trophic and radiation ulcers with profuse purulent exudation, since it is intended for use in the regeneration phase and for the prevention of radiation complications.

    The aerosol container is under pressure! Therefore, it is necessary to prevent falls, shocks, exposure to direct sunlight and heating above 45 ° C.

    After the end of the use of the preparation, the container should not be opened or burned. Do not spray on near fire or on incandescent objects.

    Keep away from sources of ignition.

    Form release / dosage:

    Aerosol for external use, 5%.

    Packaging:

    By 58 g or 116 g in containers of aluminum aerosol with valves of continuous aerosol.

    The container, together with instructions for medical use, is placed in a pack of cardboard.

    Storage conditions:

    At a temperature of 15 to 25 ° C.

    In a place inaccessible to children.

    Shelf life:

    2 years.

    The drug should not be used after the expiry date indicated on the package.
    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-003169/09
    Date of registration:24.04.2009
    The owner of the registration certificate:MIKROFARM, LLC MIKROFARM, LLC Ukraine
    Manufacturer: & nbsp
    Information update date: & nbsp08.01.2016
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