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

    Active substance: dexpanthenol 5.0 g.

    Excipients: petroleum jelly - 25,0 g, lanolin anhydrous - 15,0 g, paraffin liquid (vaseline oil) - 10,0 g, emulsion wax - 3,0 g, cetostearyl alcohol - 1,65 g, methyl parahydroxybenzoate (nipagin) - 0, 2 g, purified water - 40.15 g.

    Description:Ointment is light yellow, shades from yellowish brown to greenish-brown are possible, with a characteristic smell of lanolin.
    Pharmacotherapeutic group:Reparation of tissue 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:Dexpanthenol is a pantothenic acid derivative, which is a water-soluble vitamin B (vitamin B 5), essential as a component of coenzyme A for carbohydrate, protein and fat metabolism. Stimulates skin regeneration, normalizes cellular metabolism, increases the strength of collagen fibers. It has a regenerating, mild anti-inflammatory effect, nourishes and softens the skin. Excipients improve the therapeutic properties of the ointment.
    Pharmacokinetics:With external application dexpanthenol quickly adsorbed and converted into pantothenic acid, binds to blood plasma proteins (mainly with beta-globulin and albumin). The concentration of pantothenic acid in the blood is 0.5-1 mg / l, in blood plasma - 100 μg / l. Pantothenic acid is not metabolized in the body and is excreted unchanged by the kidneys.
    Indications:

    Violations of the integrity of the skin, caused by mechanical, chemical, temperature factors or after surgical interventions:

    - burns of different origin (including solar ones);

    - scratches, abrasions, wounds, sores;

    - poorly healing aseptic postoperative wounds;

    - dermatitis, furuncles, trophic ulcers of the lower extremities;

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

    - childcare: prevention and treatment of diaper rash in infants, activation of the healing process of the skin for minor lesions, diaper dermatitis;

    - for treatment and protection of dry skin;

    - treatment and prevention of the effects of adverse effects on the skin of environmental factors (cold, wind, humidity).

    Contraindications:

    Hypersensitivity to the components of the drug.

    Pregnancy and lactation:

    Panthenol can be used during pregnancy and during breastfeeding.

    Dosing and Administration:

    Outwardly. Ointment is applied a thin layer on the affected area, gently rubbing, 2-4 times a day (if necessary more often). In case of application on the infected skin surface, it should be pretreated with any antiseptic. Breastfeeding mothers need to lubricate the surface of the nipple with ointment after each breast-feeding.

    Breast children are given ointment after each change of underwear or water treatment. The duration of the drug depends on the individual characteristics of the course of the disease in the patient and is determined by the therapeutic effect achieved and the tolerability of the drug.

    If there is no improvement after treatment or new symptoms appear, it is necessary to consult a 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:

    Allergic reactions (including delayed due to the presence of the drugmethylparahydroxybenzoate) - urticaria, pruritus.

    Overdose:

    There were no cases of drug overdose.

    Interaction:

    Interaction with other drugs is not established.

    Special instructions:

    Do not apply to dying wounds.

    Avoid contact with eyes. Treatment of trophic ulcers and poorly healing transplants should be carried out under the supervision of the attending physician.

    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 medicine you are treating is intended for you personally, and should not be transferred to others, as it can harm them even if you have the same symptoms as you.

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

    The drug does not affect the ability to drive vehicles and engage in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.

    Form release / dosage:Ointment for external use 5%.
    Packaging:

    Ointment for external use of 5% in tubes of aluminum with bush on 25,0 g; 30.0 g or 50.0 g.Each tube, together with the instruction for medical use, is placed in a pack of cardboard.

    Storage conditions:

    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:LP-004229
    Date of registration:04.04.2017
    Expiration Date:04.04.2022
    The owner of the registration certificate:GREEN DUBRAVA, CJSC GREEN DUBRAVA, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp16.05.2017
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