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

    1 g of ointment contains:

    active substance: dexpanthenol 50.0 mg;

    Excipients: phenonip 4,0 mg, lanolin -160,0 mg, beeswax white 50,0 mg, paraffin white soft 210,8 mg, dimethicone 5,0 mg, emulsifier LANETTE SX 20.0 mg, propylene glycol 20.0 mg, butyl hydroxy anisole 0.1 mg, butyl hydroxytoluene 0.1 mg, decamethylcyclopentasiloxane 20.0 mg, magnesium sulfate heptahydrate 5.0 mg, proteine ​​B 295.0 mg, purified water 160.0 mg .

    Description:

    Homogeneous ointment light yellow color 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 derivative of pantothenic acid. Pantothenic acid - water-soluble vitamin B - is an integral part of coenzyme A. Stimulates skin regeneration, normalizes cellular metabolism, increases the strength of collagen fibers. Increased demand for pantothenic acid is observed when the skin or tissues are damaged, and its deficiency can be compensated for by local application of D-Panthenol. Optimum molecular weight, hydrophilicity and low polarity make it possible to penetrate all layers of the skin.It has a regenerating, weak anti-inflammatory effect.

    Pharmacokinetics:When topical application is rapidly absorbed and converted to pantothenic acid, binds to plasma proteins (mainly with beta-globulin and albumin).
    Indications:

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

    - burns of different origin (including solar);

    - scratches, abrasions, wounds, sores;

    - poorly healing skin grafts, aseptic postoperative wounds.

    Inflammatory processes on the skin: dermatitis, furuncles, trophic ulcers of the lower extremities; care for the skin around the tracheostist, gastrostom and colostrum.

    Treatment and prevention of the effects of adverse effects on the skin of environmental factors (cold, wind, dampness).

    Children - with diaper dermatitis, scratches and minor irritation after exposure to the sun, ultraviolet and X-rays, for the treatment and prevention of diaper rash.

    Cracks and inflammations of the nipples of the breast in nursing mothers.

    It is also used for the treatment and protection of dry skin as a source of neutral fats and dexpanthenol.

    Contraindications:

    Hypersensitivity to one of the components of the drug.

    Pregnancy and lactation:

    D-Panthenol, ointment for external use, can be used during pregnancy and lactation.

    Dosing and Administration:

    Ointment is applied 2-4 times a day (if necessary more often). Apply a thin layer on the affected area of ​​the skin, lightly rubbing. In case of application on the infected skin surface, it should be pretreated with any antiseptic.

    Breastfeeding mothers lubricate the surface of the nipple with ointment after each breast-feeding.

    Ointment is also used in children, including newborns. Breast children are given ointment after each change of underwear or water treatment.

    The duration of the drug and the possibility of a repeat course of treatment depend 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.

    Side effects:

    Side effects are extremely rare. Minor allergic reactions are possible.

    Overdose:

    Cases of overdose are not marked.

    Interaction:The interaction of D-Panthenol ointment with other drugs for external use is not established.
    Special instructions:

    Treatment of trophic ulcers and poorly healing skin grafts should be performed under the supervision of the attending physician.

    Do not apply to dying wounds.

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

    The drug does not affect the ability to drive vehicles and mechanisms.

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

    For 25 g, 50 g of the drug at aluminum tube, coated twice with a protective varnish, with a sealed hole and a plastic cap.

    The tube together with the instruction for use is placed in a cardboard box.

    Storage conditions:

    At a temperature not higher than 25 ° C, out of the reach of children.

    Shelf life:

    2 years.

    Do not use after expiry date.

    Terms of leave from pharmacies:Without recipe
    Registration number:П N011108
    Date of registration:29.06.2010 / 17.10.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:Yadran Galensky Laboratories a.o.Yadran Galensky Laboratories a.o. Croatia
    Manufacturer: & nbsp
    Representation: & nbspYadran Galen Laboratory as.Yadran Galen Laboratory as.Croatia
    Information update date: & nbsp17.03.2017
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