Octenisept disinfectant fl. 50ml

Dosage form

Ready-to-use solution in the form of a clear, colorless liquid with a weak specific odor.

Release form

Solution for local and external use 250 ml, bottle

Structure

100 g of solution contains:

active substances: 0.1 g octenidine dihydrochloride, 2.0 g phenoxyethanol.

Other components: (3-amidopropyl coconut fatty acid) - dimethylazanium acetate, D-sodium gluconate, glycerol 85%, sodium chloride, purified water, sodium hydroxide.

pharmachologic effect

The OCTENISEPT" agent has antimicrobial activity against gram-positive and gram-negative bacteria, including causative agents of nosocomial infections, mycobacterium tuberculosis, fungi of the genus Candida, as well as hepatitis B and HIV viruses.

According to the parameters of acute toxicity when administered into the stomach and applied to the skin, the "OCTENISEPT" agent, according to GOST 12.1.007-76, belongs to the 4th class of low-hazard compounds.

Local irritating, skin resorptive and sensitizing properties in the recommended modes of use were not detected in the agent.

The safety of the product is controlled by the volatile component - 2-phenoxyethanol.

MPC in the air of the working area of ​​2-phenoxyethanol - 2 mg / m3.

Side effects

Possible short-term burning sensation at the site of application.

Bitter taste is possible when rinsing the mouth.

Special conditions

PRECAUTIONS.

The "OCTENISEPT" product is used only for external use.

FIRST AID MEASURES

1. If the product gets into the eyes, rinse them abundantly with running water and drip a 20% or 30% sodium sulfacyl solution.

2. If the agent enters the stomach, rinse the stomach with plenty of water and take adsorbents (for example, activated carbon, burnt magnesia: 1-2 tablespoons per glass of water), provide peace and warmth to the victim.

Do not use Octenisept® after the expiration date.

After opening the bottle, use the drug for no more than 5 years, but no longer than the specified expiration date.

Indications

The "OCTENISEPT" product is intended for the treatment of the skin of the operating and injection fields of patients in medical institutions.

In traumatology for the treatment of wound and burn surfaces.

In dermatovenerology for the prevention and treatment of mycoses of the feet and interdigital mycoses.

Contraindications

hypersensitivity to the components of the drug, allergic reactions.

Drug interactions

Do not mix with other drugs, especially with iodine-containing antiseptics.

Dosage

1. Treatment of the skin of the operating field: the skin is wiped with double-separate sterile gauze tampons, abundantly moistened with the agent.

The holding time after the end of processing is 2 minutes.

On the eve of the operation, the patient takes a shower (bath), changes linen.

2. Treatment of the skin of the injection field: the skin is wiped with a sterile cotton swab, abundantly moistened with the agent.

The holding time after the end of processing is 1 minute.

In accordance with the indications, the skin and mucous membranes are thoroughly and completely treated with Octenisept.

Usually, the treatment is carried out with two or three tampons abundantly moistened with the drug, which alternately rub the affected area.

Due to the anatomical and physiological characteristics, this method is preferable for the treatment of the mucous membrane.

The preparation can be applied to easily accessible areas of the skin by spraying with a mechanical spray bottle.

The drug can also be used to rinse the mouth and rinse the vaginal area.

The required exposure time depending on the area of ​​application:

Anogenital area - 1 minute.

Before bladder catheterization - 1 minute.

Antiseptic skin treatment before surgery - 2 minutes.

Oral cavity: treatment with tampons for 2 minutes, rinsing for 1 minute.

Wound surfaces - 1 minute.

For profile purposes

Name ENG

OCTENISEPT

Clinical and pharmacological group

Antiseptic for external and local use

ATX code

Other antiseptics and disinfectants

Dosage

0.1g / 100ml + 2g / 100ml x 50ml

Structure

100 g of solution contains: active substances: 0.1 g of octenidine dihydrochloride, 2.0 g of phenoxyethanol.

Other components: (3-amidopropyl coconut fatty acid) - dimethylazanium acetate, D-sodium gluconate, glycerol 85%, sodium chloride, purified water, sodium hydroxide.

Storage conditions and periods

In a dark place at a temperature not exceeding 25 degrees.

INN / Active ingredient

octenidine dihydrochloride + phenoxyethanol

Specifications

Category

Antiseptics and disinfectants

Scope of the drug

General

Release form

Solution

Manufacturer country

Germany

Package quantity, pcs

one

Minimum age from

From birth

Way of introduction

Locally

,

Outwardly

,

Vaginally

,

On the mucous membrane

Vacation conditions

Without recipe

Volume, ml.

50 ml

Brand name

ToExternalID_140431186

The amount of the dosage form in the primary package

50 ml

Primary packaging type

Polyethylene bottle

Pharmaco-therapeutic group

Antiseptic

Anatomical and therapeutic characteristics

D08AX Other antiseptics and disinfectants

Dosage form

Solution for external use

Dosage (volume) of the substance in the preparation

0.1 g octenidine dihydrochloride, 2.0 g phenoxyethanol

Expiration date in days

1095

The target audience

Children

Package weight, g

350

Mode of application

:

1. Treatment of the skin of the operating zero: the skin is wiped with double-separate sterile gauze swabs, abundantly moistened with the agent. The holding time after the end of processing is 2 minutes. On the eve of the operation, the patient takes a shower (bath), changes linen. < br> 2. Treatment of the skin of the injection field: the skin is wiped with a sterile cotton swab, abundantly moistened with the agent. The holding time after the end of processing is 1 minute. < br> In accordance with the indications, the skin and mucous membrane are thoroughly and completely treated with Octenisept. Usually, the treatment is carried out with two or three tampons abundantly moistened with the drug, with which the affected area is rubbed in turn. Due to the anatomical and physiological characteristics, this method is preferable for the treatment of the mucous membrane. < br> The preparation can be applied to easily accessible areas of the skin by spraying with a mechanical spray bottle. The drug can also be used to rinse the mouth and rinse the vaginal area. < br> Necessary exposure time depending on the area of ​​application: < br> Anogenital area - 1 minute. < br> Before bladder catheterization - 1 minute. < br> Antiseptic skin treatment before surgery - 2 minutes. < br> Oral cavity: treatment with tampons for 2 minutes, rinsing for 1 minute. < br> Wound surfaces - 1 minute. < br> In order to prevent fungal diseases, the skin of the interdigital spaces and feet is treated with the preparation before and after visiting public places (swimming pool, sauna, etc.).In the treatment of fungal diseases of the skin of the interdigital spaces and feet, the affected areas are treated with the drug in the morning and evening for 14 days.

Information on technical characteristics, delivery set, country of manufacture "