1 cylinder of 58.5 g supports a dekspantenol of 2.5 g, allantoin of 0.05 g; 1 cylinder of 117 g supports a dekspantenol of 5 g, allantoin of 0.1 g
Composition of medicine:
active ingredient:
excipients: Euxyl®PE 9010, containing 90% of phenoxyethanol and 10% of ethylhexylglycerin (in terms of phenoxyethanol), DL пантолактон, cetostearyl alcohol, potassium cetylphosphate, glycerin, dimetikon DM 100, the water purified, freon 134a.

Dosage form.
Aerosol skin.

Drug at an exit forms foam of white color of a cylinder.
Name and location of the producer.
LLC Pharmaceutical Company Zdorovye.
Ukraine, 61013, Kharkiv, Shevchenko St., 22.

Pharmacotherapeutic group.

Drugs for treatment of wounds and cankers. Code of automatic telephone exchange D03A X03.

Active ingredient of medicament is dekspantenol – B5 provitamin and allantoin. In skin cells dekspantenol quickly turns into pantothenic acid and works as vitamin. Dekspantenol quicker, than pantothenic acid, is absorbed after external use. Pantothenic acid is a component of coenzyme of A.V to this form acetyl coenzyme A plays the central role in metabolism of each cell. Pantothenic acid is, thus, necessary for forming and healing of the damaged skin and mucous membranes.
Dekspantenol at external use is quickly absorbed by skin. In skin cells dekspantenol turns into pantothenic acid at once and comes to endogenous fund of this vitamin.
In blood pantothenic acid communicates with? - globulin and albumine of blood plasma. Pantothenic acid is not exposed to biotransformation, she leaves not changed (60-70% are removed with urine, the others – with excrements). Allantoin has the anti-inflammatory, pulling together effect, softens and stimulates granulation of epidermis. Allantoin regenerates an epithelium, reduces morbidity.

Indications.

Various injuries of skin and mucous membranes, including grazes, burns, aseptic postoperative wounds, skin transplants, bullous and bubbly dermatitis.

Contraindications.
Hypersensitivity to any of medicament components.

Special cautions.

Aerosol can is under pressure therefore it is necessary to prevent falling, blows, influence of direct sunshine and should not be heated to temperature over 25 °C. Not to apply medicament on the becoming wet wounds. At treatment of wounds and burns, medicament is used at a regeneration stage. Upon termination of medicament use not to open and not to burn a cylinder. Not to spray medicament near naked flame or on the heated objects. Not to allow hit in eyes. At accidental hit of medicament in eyes they need to be washed with water carefully. There are no restrictions concerning use for children and people of advanced age, but children should use medicament only under observation of adults.

Use during pregnancy or feeding by a breast.
do not have Contraindications. In the period of a lactation medicament is applied to skin of mammary glands after feeding by a breast.

Ability to influence speed of response at control of motor transport or work with other mechanisms.
influences of medicament on speed of response Given relatively at control of motor transport or work with other mechanisms are absent.

Children.
Drug is used in pediatric practice after consultation with the doctor and only under observation of adults.

Route of administration and doses.
At use to hold vertically the valve up. Before use the cylinder should be stirred up well. At the first use of a cylinder the spraying only of gas within several seconds is possible, and then foam appears. Aerosol apply one or several times in day by uniform drawing on the respective damaged sites. Duration of treatment depends on a course of the disease and is defined by the doctor individually. Not to use about an open flame or strongly heated objects. A cylinder under pressure. After use not to sort, not to throw a cylinder into fire.
Overdose.
there Are no data on medicament overdose.

Side effects.
In isolated cases local allergic reactions which demand medicament withdrawal can arise.

Interaction with other medicines and other types of interactions.
Panthenol can strengthen action of the depolarizing muscle relaxants (succinylcholine, dekametony) and to reduce action of not depolarizing muscle relaxants (D-tubocurarine, galamin) because stimulates acetosincaline synthesis.

Expiration date.
2 years.
not to apply after the expiry date specified on packing.

Storage conditions.
to Store in original packing at a temperature not higher than 25 wasps. Not to freeze.
to Store out of children's reach.

Packing.
Aerosol skin on 58.5 g or on 117 g in a cylinder in a box.

Category of release.
Without prescription.

Description of goods is certified by the Health producer .

Editorial group Date of creation: 21.01.2021 Date of updating: 05.04.2023 Yashch_shin Mart of a =vgen_vn Author Oleksander V_ktorovich Sevryukov Reviewer

Pay attention!

Description of the medicament HeppiDerm Forte aeroz. foam nakozhn. cylinder 117g on this page — the simplified author's version of website apteka911 created on the basis of the instruction(s) for use. Before acquisition or use of medicament you have to consult with the doctor and study the original instruction of the producer (it is applied to each packing of drug).

Information on medicament is provided to

only with the fact-finding purpose and should not be used as the management to self-treatment. Only the doctor can make the decision on prescribing of medicament and also define doses and ways of its use.

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Frequently asked questions

How much is HeppiDerm Forte aeroz. foam nakozhn. cylinder 117g?

Prices on HeppiDerm Forte aeroz. foam nakozhn. cylinder 117g begin from 61.17 UAH for packing. whether

Can give this medicine to children?

On doctor's orders and under supervision of adults. It is necessary to consult with your attending physician more in details.

What storage conditions at HeppiDerm aerosol (Health)?

It agrees with the instruction storage temperature HeppiDerm (Health) makes from 2 °C to 25 °C. To store out of children's reach.

What analogs at HeppiDerm No. 1 aerosol?

Analogues with similar therapeutic effect are:

• Bepanten cream of 5% of a tube of 100 g
• Bepanten cream of 5% of a tube of 30 g
• Bepanten ointment of 5% of a tube of 100 g

What country of origin at HeppiDerm (Health)?

Country the producer at HeppiDerm (Health) - Ukraine.

Structure

Active ingredient: 1 g of medicament (without freon 134a) supports a dekspantenol of 50 mg, allantoin of 1 mg;

Excipients: DL пантолактон, cetostearyl alcohol, potassium cetylphosphate, glycerin, dimetikon DM 100, the water purified, freon 134a; Euxyl ^® PE 9010 (Euksil) containing phenoxyethanol and ethylhexylglycerin.

Dosage form

Foam skin.

Main physical and chemical properties: medicament at an exit forms foam of white color of a cylinder.

Pharmacological group

Drugs for treatment of wounds and ulcers. ATX D03A X03 code.

Pharmacological properties

Pharmacodynamics

Active ingredient of medicament is dekspantenol - provitamin In ₅ which has the same biological efficiency, as well as pantothenic acid, thanks to an intermediate metabolism of substances. In skin cells dekspantenol quickly turns into pantothenic acid. Pantothenic acid and its salts are water-soluble vitamins which in the form of coenzyme A participate in many metabolic processes. Pantothenic acid, thus, is necessary for forming and healing of the damaged skin and mucous membranes.

Topical administration of a dekspantenol can compensate to

increased need of the injured skin and/or mucous membranes for pantothenic acid.

Allantoin has the anti-inflammatory, pulling together effect, softens and stimulates granulation of epidermis. Regenerates an epithelium, reduces morbidity.

Pharmacokinetics

Active substance is absorbed by skin. Detailed researches on metabolism of active agent in skin and mucous membranes did not carry out.

to Apply

Indication

at various injuries of skin and mucous membranes, including in grazes, burns, aseptic postoperative wounds, skin transplants, bullous and bubbly dermatitis.

Contraindication

Hypersensitivity to medicament components.

to

Interaction with other medicines and other types of interactions

to

At use of medicament according to indications does not know interaction with other medicines.

Feature of use

Aerosol can is under pressure therefore it is necessary to prevent falling, blows, influence of direct sunshine and heating to temperature more than 50 °C.

a cylinder not to open and not to burn

After the end of use of drug. Not to spray medicament near naked flame or on the heated objects. Not to allow hit in eyes. At accidental hit of medicament in eyes they need to be washed with water carefully.

Use during pregnancy and feeding by a breast

Dekspantenol gets through a placental barrier by active transport process and into breast milk in proportion of its absorption.

As system availability of a dekspantenol after topical administration is unknown to

, in need of use of medicament during pregnancy and feeding by a breast on big sites of skin it is necessary to weigh carefully advantage of use of medicament for mother and possible risk for the fruit/child. During pregnancy the medicament use on doctor's orders is possible. At use for treatment of nipple cracks during feeding by a breast medicament should be washed away before feeding.

Ability to influence speed of response at control of transport or other mechanisms

Special cautions are absent.

Route of administration and doses

Drug evenly to spray

on the damaged site one or several times in day. Spraying drug, to hold a cylinder vertically, the valve up. To receive quality foam, it is necessary to stir up vigorously a cylinder before each use, especially if it was not used for a long time. If medicament is used for the first time, only gas before foam is formed first can be sprayed.

Duration of treatment depends on a look and a course of the disease and is defined after consultation with the doctor.

If to use medicament on area of the person, it should not be sprayed directly on the person. It is desirable to spray medicament on a hand and to distribute it on the corresponding parts of the face. Not to spray medicament in eyes, directly in a mouth or in a nose.

Children.

to Children medicament should be used on doctor's orders and under supervision of adults.

Overdose

to

At topical administration of medicament the cases of overdose are unknown to

.

Dekspantenol, even in high doses, is well had and it is considered non-toxic. The hypervitaminosis is unknown.

Side reactions

Allergic reactions: very seldom there can be allergic contact dermatitis and irritation of skin which are shown such symptoms as an itching, an erythema, eczema, rash, urticaria and bubbles.

Expiration date

3 years.

Storage conditions

to Store

in original packing at a temperature not above 25 °C.

not to freeze

.

to Store

out of children's reach.

Packing

On 58.5 g or on 117 g in the cylinder completed with the valve foam-forming with the spray and a protective cap in a box.

Category of release

Without prescription.

Producer

LLC Pharmaceutical Company Zdorovye.

Location of the producer and its address of the place of implementation of activity

Ukraine, 61013, city of Kharkiv, Shevchenko Street, 22.