Bepanten 5% 30g cream
- $18.20
Sku:
316fcb78f7eb
Ingredient:
Dexpanthenol
The instruction for medical use
of BEPANTEN® medicine
the Trade name
of Bepanten®
the International unlicensed
name Dekspantenol Lekarstvennaya a form
Cream for external use of 5%
Structure
of 1 g of cream contains
active agent - dekspantenol 50 mg
excipients: DL пантолактон, phenoxyethanol, amfizol To, cetyl alcohol, stearyl alcohol, lanolin, an isopropyl myristate, propylene glycol, water purified.
The description
Soft, elastic, homogeneous, opaque cream from white till pale yellow-white color with a slight specific smell.
Pharmacotherapeutic group
the Other drugs promoting normal scarring.
The code of automatic telephone exchange D03AX03
the Pharmacological
Dekspantenol Pharmacokinetics properties is quickly absorbed by skin. Dekspantenol turns into pantothenic acid and unites with an endogenous part of vitamin. In blood pantothenic acid contacts proteins of plasma, is removed in not changed look – 60-70% with urine, the rest through a GIT.
The pharmacodynamics
Dekspantenol is Bepantena® active component, quickly turns in cells into pantothenic acid. 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.
Indications
- for acceleration (activation) of process of healing of skin at small damages, reddenings, cracks, grazes, skin irritations, an erythema from diapers, slight burns, sunblisters, chronic ulcers, decubituses, at skin transplantation and an erosion of a neck of the uterus
- prevention and treatment of an intertrigo at babies
- mammary gland care during feeding: treatment of dryness and nipple cracks
- prevention and treatment of xeroderma at disturbance of integrity of its covers
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).
Contraindications
- the increased individual sensitivity to drug components
Medicinal interactions
interaction Cases with other drugs are unknown.
The special
instructions Pregnancy and the period of breastfeeding
Cream can be used during pregnancy and during breastfeeding.
Features of influence of medicine on ability to run the vehicle and potentially dangerous mechanisms.
Бепантен® does not affect ability to run vehicles and other mechanisms.
Overdose
Cases of overdose are unknown.
The form of release and packing
On 30 g of drug place in an aluminum tuba. On 1 tuba with the instruction for medical use in the state and Russian languages place in a pack from cardboard.
To Store storage conditions at a temperature not above 25 °C.
To store out of children's reach!
The period of storage
Drug should not be used 3 years 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 Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of a product (goods)
of Bayer of KAZ LLP in
Republic of Kazakhstan, 050057 Almaty, Timiryazev St., 42, Expo City, peahens. 15, floor 3.
ph. +7 727 258 80 40 (148)
fax: +7 727 244 70 01
e-mail: kz.claims@bayer.com
of BEPANTEN® medicine
the Trade name
of Bepanten®
the International unlicensed
name Dekspantenol Lekarstvennaya a form
Cream for external use of 5%
Structure
of 1 g of cream contains
active agent - dekspantenol 50 mg
excipients: DL пантолактон, phenoxyethanol, amfizol To, cetyl alcohol, stearyl alcohol, lanolin, an isopropyl myristate, propylene glycol, water purified.
The description
Soft, elastic, homogeneous, opaque cream from white till pale yellow-white color with a slight specific smell.
Pharmacotherapeutic group
the Other drugs promoting normal scarring.
The code of automatic telephone exchange D03AX03
the Pharmacological
Dekspantenol Pharmacokinetics properties is quickly absorbed by skin. Dekspantenol turns into pantothenic acid and unites with an endogenous part of vitamin. In blood pantothenic acid contacts proteins of plasma, is removed in not changed look – 60-70% with urine, the rest through a GIT.
The pharmacodynamics
Dekspantenol is Bepantena® active component, quickly turns in cells into pantothenic acid. 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.
Indications
- for acceleration (activation) of process of healing of skin at small damages, reddenings, cracks, grazes, skin irritations, an erythema from diapers, slight burns, sunblisters, chronic ulcers, decubituses, at skin transplantation and an erosion of a neck of the uterus
- prevention and treatment of an intertrigo at babies
- mammary gland care during feeding: treatment of dryness and nipple cracks
- prevention and treatment of xeroderma at disturbance of integrity of its covers
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).
Contraindications
- the increased individual sensitivity to drug components
Medicinal interactions
interaction Cases with other drugs are unknown.
The special
instructions Pregnancy and the period of breastfeeding
Cream can be used during pregnancy and during breastfeeding.
Features of influence of medicine on ability to run the vehicle and potentially dangerous mechanisms.
Бепантен® does not affect ability to run vehicles and other mechanisms.
Overdose
Cases of overdose are unknown.
The form of release and packing
On 30 g of drug place in an aluminum tuba. On 1 tuba with the instruction for medical use in the state and Russian languages place in a pack from cardboard.
To Store storage conditions at a temperature not above 25 °C.
To store out of children's reach!
The period of storage
Drug should not be used 3 years 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 Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of a product (goods)
of Bayer of KAZ LLP in
Republic of Kazakhstan, 050057 Almaty, Timiryazev St., 42, Expo City, peahens. 15, floor 3.
ph. +7 727 258 80 40 (148)
fax: +7 727 244 70 01
e-mail: kz.claims@bayer.com
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