Ethanol 70

INSTRUCTIONS FOR MEDICAL USE OF THE MEDICINAL PRODUCT ETHANOL 70 (ETHANOL 70)

Composition:

Active substance:
ethanol;

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

Pharmaceutical form.
70 % topical solution.

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

Pharmacotherapeutic group.
Antiseptics and disinfectants.
ATC Code
D08A X08.

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, felons, infiltrates, mastitis in the initial stages. For wiping and compresses. Surgical hand disinfection.

Contraindications.

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

Special precautions.

In case of skin redness or irritation, discontinue use of the product and wash the area with water.

Avoid contact of the product with eyes!

Interaction with other medicinal products and other forms of interaction.

When ethanol is used topically, 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 possible only if the expected benefit to the mother outweighs the potential risk to the fetus or infant.

Ability to influence reaction rate while driving 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 (for burn prevention), ethanol should be diluted with water in a 1:1 ratio.

Children.

Use as directed by a physician.

Overdose.

With external application, cases of overdose are unknown.

Side effects.

With local use, skin or mucous membrane irritation is possible.

If any adverse reactions occur, consult a doctor.

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, 100 ml in polymer bottles.

1 L, 5 L, 10 L, 20 L in polymer cans (for supply to medical institutions).

Prescription status. Prescription only.

Manufacturer.

PP "Kilaff".

Manufacturer's location and address of business activity.

6 Kharkivska Street, Sumy, Sumy region, 40035, Ukraine.