Azelik gel d / nar. approx. 15% tube 15g

Release form, composition and packaging

Gel for external use 15% white or almost white, a weak specific odor is allowed.

100 g

azelaic acid in terms of 100% substance 15 g

benzoic acid - 0.1 g, methylpyrrolidone - 4 g, squalane - 1 g, propylene glycol - 8 g, disodium edetate - 0.1 g, sodium hydroxide - 0.25 g, dimethicone 100 cst - 1 g, macrogol cetostearyl ether - 1.4 g, carbomer interpolymer ( type A) - 1.4 g, purified water - up to 100 g.

5 g - aluminum tubes (1) - cardboard packs.

15 g - aluminum tubes (1) - cardboard packs.

30 g - aluminum tubes (1) - cardboard packs.

pharmachologic effect

The drug is for external use.

Has bacteriostatic activity against Propionibacterium acne and Staphylococcus epidermidis, reduces the production of fatty acids that contribute to acne.

Reduces the formation of comedones.

Influencing the process of keratinization of epidermal cells, it inhibits the growth and activity of abnormal melanocytes that cause hyperpigmentation such as melasma.

Has anti-acne, depigmenting effect.

Pharmacokinetics

Suction

After application to the skin, it penetrates the epidermis and dermis, 3.6% of the total dose is absorbed into the systemic circulation.

Metabolism and excretion

Part of the absorbed acid is excreted by the kidneys unchanged, part - in the form of dicarboxylic acids (C7, C5), formed as a result of beta-oxidation.

Indications for use

- acne (acne vulgaris)

- rosacea.

Contraindications for use

- hypersensitivity to drug components.

The drug should be used with caution during pregnancy and lactation (breastfeeding).

Dosage regimen

Apply externally.

The gel should be applied to previously thoroughly washed (with water or cleansed with a mild cosmetic cleansing agent) and dried face skin.

The gel is applied in a thin layer on the affected skin 2 times / day (morning and evening) and rubbed lightly.

Approximately 2.5 cm of gel is sufficient for the entire face.

In patients with acne vulgaris, a marked improvement is usually seen after 4 weeks.

For best results, use of the drug should be continued for several months.

Overdose

Currently, no cases of drug overdose have been described.

Side effect

On the part of the skin and subcutaneous fat: at the beginning of treatment, a local irritating effect, hyperemia and peeling of the skin, burning sensation, erythema, itching, usually disappearing during treatment, are possible

possibly - allergic skin reactions.

Drug interactions

Can be used in combination with other drugs to treat acne.

Application during pregnancy and lactation

During pregnancy and during breastfeeding, it is used only if the intended benefit of therapy to the mother outweighs the risk to the fetus or infant.

special instructions

In cases of severe severe skin irritation in the first weeks of treatment, the gel can be applied 1 time / day

short-term drug withdrawal is also possible.

After the symptoms of skin irritation have disappeared, regular use of the drug should be resumed at the recommended dose.

Avoid getting the drug in the eyes, as well as on the mucous membranes of the nose, lips and mouth, in case of accidental contact, rinse immediately with water.

During treatment, it is necessary to protect the skin from the entire spectrum of solar radiation.

Name ENG

AZELIC

Clinical and pharmacological group

Drug with antiproliferative and antibacterial action for the treatment of acne, hyperpigmentation

Dosage

15% x 15g

Structure

100 g of gel contain: active substance: azelaic acid in terms of 100% substance - 15 g

excipients: benzoic acid 0.1 g, methylpyrrolidone 4 g, squalane 1 g, propylene glycol 8 g, disodium edetate 0.1 g, sodium hydroxide 0.25 g, dimethicone 1 g, macrogol cetostearate 1.4 g, carbomer interpolymer 1 , 4 g, purified water up to 100 g.

Indications

Acne decreased production of fatty acids

INN / Active ingredient

azelaic acid

Storage conditions and periods

At a temperature not exceeding 25 degrees (do not freeze).

Expiration date: 2 years

Contraindications

Hypersensitivity to drug components.

The drug should be used with caution during pregnancy and lactation (breastfeeding).

Specifications

Category

Acne

Scope of the drug

Dermatology

Release form

Gel

Manufacturer country

Russia

Package quantity, pcs

one

Scope of application

Dermatology

Way of introduction

On the skin

Vacation conditions

Without recipe

Brand name

Akrikhin

The amount of the dosage form in the primary package

15 g

Primary packaging type

Tuba

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

Acne rash treatment

Anatomical and therapeutic characteristics

D10AX03 Azelanic acid

Dosage form

Gel for external use

The target audience

Adult

Expiration date in days

730

Package weight, g

thirty

Mode of application

:

Outwardly.

The gel should be applied to previously thoroughly washed (with water or cleansed with a mild cosmetic cleansing agent) and dried face skin.

The gel is applied in a thin layer on the affected skin 2 times / day (morning and evening) and rubbed lightly.

Approximately 2.5 cm of gel is sufficient for the entire face.

Information on technical characteristics, delivery set, country of manufacture