Universal reference book for medicines
Product name: BASIRON AC (BASIRON AC)

Active substance: benzoyl peroxide

Type: Acne treatment

Manufacturer: Laboratoires GALDERMA (France)
Composition, form of production and packaging
?
Gel for external use 2.5% 1 g
benzoyl peroxide 25 mg

Excipients: sodium hydroxide, distilled water, silicon colloid anhydrous, disodium edetate, propylene glycol, poloxamer 182, acrylate copolymer, carbomer 940 (carbopol 980), sodium dioctyl sulfosuccinate, glycerol.

40 g - aluminum tubes (1) - packs of cardboard.

40 g - polyethylene tubes (1) - cardboard packs.

?
Gel for external use 5% 1 g
benzoyl peroxide 50 mg

Excipients: sodium hydroxide, distilled water, silicon colloid anhydrous, disodium edetate, propylene glycol, poloxamer 182, acrylate copolymer, carbomer 940 (carbopol 980), sodium dioctyl sulfosuccinate, glycerol.

40 g - polyethylene tubes (1) - cardboard packs.

?
Gel for external use 10% 1 g
benzoyl peroxide 100 mg

Excipients: sodium hydroxide, distilled water, silicon colloid anhydrous, disodium edetate, propylene glycol, poloxamer 182, acrylate copolymer, carbomer 940 (carbopol 980), sodium dioctyl sulfosuccinate, glycerol.

40 g - polyethylene tubes (1) - cardboard packs.

INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2014.

PHARMACHOLOGIC EFFECT

Benzoyl peroxide exhibits antimicrobial activity against Propionibacterium acnes and Staphylococcus epidermidis.
It has a keratolytic effect, improves oxygenation of tissues, inhibits the production of sebum in the sebaceous glands.
PHARMACOKINETICS

Penetration of benzoyl peroxide through the skin is low.
The bulk of the benzoyl peroxide is converted to benzoic acid, which after absorption is introduced into the systemic circulation and rapidly excreted by the kidneys. There is no cumulation in the tissues. Dense application of Bazirone AS in therapeutic doses does not lead to side effects of systemic action.
INDICATIONS

- acne.

DOSING MODE

Outwardly.
With a gentle touch, apply the gel uniformly to the affected area 1 or 2 times a day (morning and evening) on ​​clean, dry skin. The therapeutic effect develops after 4 weeks of treatment, a persistent improvement after 3 months of treatment.
Repeated treatment is possible after consultation with a doctor.

SIDE EFFECT

In rare cases, local irritation (redness, peeling, dry skin, burning sensation).
In such cases, it is recommended to reduce the frequency of application.
In rare cases, allergic contact dermatitis may occur.

CONTRAINDICATIONS

- hypersensitivity to one of the incoming ingredients of the drug;

- Children under 12 years old.

PREGNANCY AND LACTATION

Controlled clinical trials of the drug during pregnancy and lactation were not conducted.
For a long time of clinical use of Baziron AS there were no cases of toxic effects on the fetus or malformations. The use of Baziron AS gel during pregnancy and breastfeeding is possible when the intended benefit to the mother exceeds the potential risk to the fetus.
APPLICATION FOR CHILDREN

Contraindicated in children under 12 years.

SPECIAL INSTRUCTIONS

Avoid getting Baziron AS gel on the mucous membranes of the eyes, mouth and nose.
In case of accidental ingestion of the drug on mucous membranes, rinse thoroughly with warm water.
It is not recommended simultaneous use of funds with exfoliating, drying or irritating effect (for example, products containing alcohol).

Sun and ultraviolet irradiation are not recommended, which are an additional cause of skin irritation.

TERMS OF RELEASE FROM PHARMACY

Without recipe.

TERMS AND CONDITIONS OF STORAGE

At a temperature of no higher than 25 ° C.
Keep out of the reach of children. Shelf life - 3 yea
Alphabetical index of medicines:
A  B  V  G  D  E  J
Z  I  Y  K  L  M  N
O  P  R  S  T  U  F
H  C  CH  SH  E  U  Y
Rambler's Top100
Privacy policy:
Copyright 2009 - 2017. Universal reference book of medicines. All rights reserved.
When using site materials, an active hyperlink is required!