ETHYL ALCOHOL 96%

INSTRUCTION
for medical use of medicinal product

ETHYL ALCOHOL 96 %
(ETHYL ALCOHOL 96 %)

Composition:

Active substance: ethanol;

not less than 95.1% v/v (92.6% w/w) and not more than 96.9% v/v (95.2% w/w) of ethanol, as well as water.

Pharmaceutical form.

Solution for external use.

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

Pharmacotherapeutic group.

Antiseptics and disinfectants.

ATC Code D08AX08.

Pharmacological properties.

Pharmacodynamics.

When applied externally, exerts antiseptic, disinfectant, and local irritant effects. Ethanol coagulates proteins and is active against Gram-positive and Gram-negative bacteria as well as viruses. Exerts an astringent ("tanning") effect on skin and mucous membranes.

Pharmacokinetics.

Not absorbed through the skin when applied locally.

Clinical characteristics.

Indications.

For disinfection of hands.

Contraindications.

Increased individual sensitivity. Acute inflammatory skin conditions. Children under 14 years of age.

Special precautions.

If redness or irritation of the skin occurs, discontinue use and wash the area 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 instructions.

Use during pregnancy or breastfeeding.

During pregnancy and breastfeeding, the product should be used only when the expected benefit to the mother outweighs the potential risk to the fetus or infant.

Ability to affect reaction rate when driving or operating machinery.

Does not affect.

Method and dosage of administration.

Apply externally — to the skin using cotton swabs or wipes.

Children.

Do not use in children under 14 years of age.

Overdose.

With external use, cases of overdose are unknown.

Adverse reactions.

With local application — irritation of the skin or mucous membranes.

If any adverse effects occur, consult a physician.

Shelf life.

5 years.

The medicinal product must not be used after the expiry date stated on the packaging.

Storage conditions.

Store in the original packaging at a temperature not exceeding 25 °C. Avoid contact with open flame.

Keep out of reach of children.

Packaging.

100 ml in glass or polymer bottles.

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

Prescription status.

By prescription.

Manufacturer.

PP ↔Kilaff≈.

Manufacturer's location and address of its place of business.

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

Manufacturer.

JSC ↔Biolyk≈.

Manufacturer's location and address of its place of business.

Ukraine, 24321, Vinnytsia region, city of Ladijyn, Nezalezhnosti Street, 131, Sh.

Applicant.

LLC "ZNAK YAKOSTI LYUKS".

Address of the applicant.

Ukraine, 34500, Rivne region, Sarney town, Belgorodskaya str., bld. 27.