Anolitum neutralium ANK (Solution) Instructions for Use

Marketing Authorization Holder

Ekran NPO, PJSC (Russia)

ATC Code

D08AX (Other antiseptics and disinfectants)

Dosage Form

Anolitum neutralium ANK

Solution for topical and external application: 400 ml or 450 ml fl.

Dosage Form, Packaging, and Composition

Solution for topical and external application transparent, colorless, with a slight smell of chlorine.

Excipients : sodium chloride solution 22 %.

400 ml – bottles.
450 ml – bottles.

Clinical-Pharmacological Group

Antiseptic for external and topical use

Pharmacotherapeutic Group

Antiseptic

Pharmacological Action

Anolitum neutralium ANK is an aqueous solution of a diluted sodium chloride solution passed through an electrochemical reactor that produces chlorine-oxygen and hydroperoxide oxidants (hypochlorous acid, hypochlorite ion, active oxygen compounds).

Anolitum neutralium ANK is non-toxic, has high reactivity and catalytic activity at low concentrations of active substances, disinfecting activity, cleansing and anti-inflammatory properties.

Anolitum neutralium ANK accelerates the healing of infected purulent wounds.

Pharmacokinetics

The active substances of Anolitum neutralium ANK do not have a resorptive effect on the body when applied externally or topically.

Indications

• Treatment of the skin, skin folds, mucous membranes for the purpose of disinfection and removal of organic contaminants (sweat, sebaceous gland secretions, other contaminants);
• Treatment of infected wounds, prevention of wound infection.

ICD codes

Dosage Regimen

Externally. Topically.

The prepared solution is applied to a gauze pad until it is intensively moistened, and the pad soaked in Anolitum neutralium ANK is applied to the treated inflamed or healthy area of the skin.

The application time is 10 -15 minutes. The consumption of Anolitum neutralium ANK during application therapy is 40-70 ml per 1000 cm² of skin surface, which corresponds to a dose of active substances from 4 to 7 mg – when converted to human body weight, approximately 0.06-0.1 mg/kg of body weight per one application.

After the application, the area of the skin treated with Anolitum neutralium ANK is dried for several minutes, and treatment is continued by other methods at the choice of the attending physician (dry sterile dressing, fat dressings, ointment dressings, or other methods).

The total number of applications with anolyte is 2-3 times a day. The duration of the treatment course is 5-7 days.

Adverse Reactions

Allergic reactions.

If the exposure time is increased to more than 15 minutes, skin irritation may occur.

Contraindications

• Hypersensitivity to the components of the drug;
• Basal cell carcinoma at the site of the intended treatment;
• Skin cancer at the site of the intended treatment.

Special Precautions

The synthesis of the drug in electrochemical units such as STEL ex tempore in the conditions of an operating room, dressing room, procedure room, or at the patient’s bedside is allowed.

The drug prepared ex tempore is placed in clean sterile containers and used according to the indications.

Drug Interactions

Do not use concomitantly with iodine-containing antiseptics

Storage Conditions

Store at a temperature from 15°C (59°F) to 25°C (77°F), in a place protected from light. Freezing or heating of the drug is not allowed.

Shelf Life

The shelf life is 5 days from the date of manufacture of the drug.

Dispensing Status

By prescription.

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.