ETHYLOSEPT 70

INSTRUCTION FOR MEDICAL USE OF THE MEDICINAL PRODUCT ETHYLOSEPT 70 (ETHYLOSEPT 70)

Composition:

Active substance:
ethanol;

not less than 69.3% v/v and not more than 70.7% v/v ethanol and water.

Pharmaceutical form.
Topical solution.

Main physicochemical properties:
clear, colorless, volatile, flammable liquid. Hygroscopic.

Pharmacotherapeutic group.
Antiseptics and disinfectants.
ATC code
D08AX08.

Pharmacological properties.

Pharmacodynamics.

When applied externally, exerts an antiseptic, disinfectant, and local irritant effect. Ethanol coagulates proteins and is active against gram-positive and gram-negative bacteria as well as viruses.

Pharmacokinetics.

When applied locally, it is not absorbed through the skin.

Clinical characteristics.

Indications.

Furuncles, panaritium, infiltrates, mastitis in the initial stages. For rubbing and compresses. Surgical hand disinfection.

Contraindications.

Hypersensitivity. Should not be used in acute inflammatory skin conditions.

Precautions.

If redness or skin irritation occurs, discontinue use of the medicinal product and wash the liquid off with water.

Avoid contact with eyes!

Interaction with other medicinal products and other forms of interaction.

When ethanol is applied externally, interactions with other medicinal products are unknown.

Special precautions for use.

Use during pregnancy or breastfeeding.

During pregnancy and breastfeeding, the use of this medicinal product is only possible if the expected benefit to the mother outweighs the potential risk to the fetus or infant.

Ability to influence reaction rate when driving vehicles or operating machinery.

Has no effect.

Method of Administration and Dosage.

Externally – for rubbing, compresses, and disinfection of the skin, including hands.

For compresses and rubbing (to prevent irritation), ethanol should be diluted with water in a 1:1 ratio.

Children.

Use only as directed by a physician.

Overdose.

Cases of overdose with topical application are unknown.

Adverse reactions.

Skin or mucous membrane irritation is possible with topical use.

If any adverse effects occur, consult a physician.

Shelf life.
5 years.

Storage conditions.
Store at a temperature not exceeding 25 °C in the original packaging, in a place inaccessible to children. Avoid contact with open flame.

Packaging.
100 mL in glass bottles. 1 L, 5 L in glass bottles, 1 L,
5 L, 10 L, 20 L in polymer canisters (for supply to medical institutions).

Prescription status.
By prescription only.

Manufacturer.
JSC "Biolyk".

Manufacturer's location and address of its place of business.
131, Nezalezhnosti Str., Sh., Ladyzhyn, Vinnytsia region, 24321, Ukraine.

Marketing Authorization Holder.
FOP Knish Vitaliy Volodymyrovych.

Address of the Marketing Authorization Holder.
19, Osinnia Str., Dnipro, Dnipropetrovsk region, 49051, Ukraine.