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Bepanten® Plus 5% 30g of the cream for external use




The instruction
for medical use
of medicine

of Bepanten® Plus Torgovoye nazvaniye Bepanten® Plus

the International unlicensed name
Is not present

the Dosage form
external use Cream

1 gram of drug contains
active agents: dekspantenol 50 mg, chlorhexidina hydrochloride of 5 mg
excipients: DL пантолактон, cetyl alcohol, stearyl alcohol, paraffin white soft, liquid paraffin, lanolin, a macrogoal stearate, water purified.

The description
Homogeneous, soft, opaque cream, pale yellow color with a slight specific smell.

The pharmacotherapeutic group
Other drugs for hyper scarring treatment
the Code of automatic telephone exchange D03AX

the Pharmacological

Dekspantenol Pharmacokinetics properties is quickly soaked up in skin. Dekspantenol turns into pantothenic acid (B5 vitamin) and unites with an endogenous part of this vitamin. In blood pantothenic acid contacts proteins of plasma (b-globulins and albumine), is removed in an invariable look – 60-70% with urine,
the rest through a GIT. Chlorhexidin when drawing on skin is practically not soaked up. At oral administration chlorhexidin it is almost completely allocated with a stake.
The pharmacodynamics
Dekspantenol is active component of Bepantena® Plus, quickly turns in cells into pantothenic acid (B5 vitamin). Pantothenic acid – a component of essential coenzyme A. In the form of acetyl coenzyme A plays an important role in metabolism of a cell and improves regeneration of skin and mucous membranes. Dekspantenol easily extends at topical administration. Chlorhexidina a hydrochloride one of the most active and well transferable local antiseptic agents with bactericidal activity concerning the gram-positive bacteria, especially sensitive strains of golden staphylococcus and microorganisms involved in skin infections. It also destroys gram-negative bacteria and mushrooms (sorts Candida).
– wounds of any genesis when there is a risk of an infection: grazes, scratches, cuts, cracks, burns, ulcers, dermatitis
– treatment of chronic wounds (decubituses, ulcers standing and others)
– in a skin infection, for example, again infected eczema, neurodermatitis
– treatment of nipple cracks at nursing mothers

the Route of administration and doses
Cream put with a thin layer one or several times a day, as required on previously cleaned wound or the inflamed sites of skin and slightly rub. If necessary it is possible to use a bandage.
Duration of treatment depends on indications and efficiency of therapy.

Side effect
Is rare
– allergic reactions (urticaria, an itching).

– the increased individual sensitivity to drug components
– at damage of extensive sites of skin
– at perforation of a tympanic membrane

Medicinal interactions
interaction Cases with other drugs are unknown.
Chlorhexidina the hydrochloride is not compatible to the detergents containing anion group (saponins, sodium lauryl sulfate, sodium carboxymethylcellulose) and also to soap.

Special instructions
It is necessary to avoid contact with eyes, ears and mucous membranes. Dekspantenol together with chlorhexidiny (Bepanten® Plus) should not be applied to treatment of skin irritations which can / should not be infected (for example, a sunblister). In such cases use of cream or lotion with dekspantenoly Bepanten is recommended).
Pregnancy and the period of a lactation
Cream can be used during pregnancy and during breastfeeding (before feeding it is necessary to wash away drug).
Not to apply at damage of more extensive sites of skin during pregnancy and breastfeeding.
Features of influence of medicine on ability to run transport or potentially dangerous mechanisms

the Overdose
Symptoms does not influence: irritation of skin in rare instances (at very frequent use on the same site of skin).
Treatment. To cancel drug use. Symptomatic therapy.

The form of release and packing
On 30 g of drug place in an aluminum tuba. On 1 tuba together with the instruction for medical use in the state and Russian languages place in a cardboard pack.

To Store storage conditions at a temperature not above 25 °C.
To store out of children’s reach!

3 years
not to use a period of storage after the expiration date specified on packing

Prescription status
Without prescription

the Name and the country
of the GP Grentsakh Produktsions GmbH manufacturing organization, Germany

the Name and the country of the owner of the registration certificate
of Bayer Konsyyumer Ker AG, Switzerland

the Name and the country
of the GP Grentsakh Produktsions GmbH organization packer, Germany

the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products (goods)
of Bayer Kaz LLP in
Republic of Kazakhstan, 050057, Almaty, Timiryazeva 42, Expo City, peahens. 15, floor 3.
Tel.: + 7 (727) 258 80 40 (148)


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