Spiritool

INSTRUCTIONS FOR MEDICAL USE OF THE MEDICINAL PRODUCT SPIRTOL®

Composition:

Active substance: ethanol;

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

Pharmaceutical form. Solution for external use.

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

Pharmacotherapeutic group.

Antiseptics and disinfectants.

ATC code D08AX08.

Pharmacological properties.

Pharmacodynamics.

Exerts antiseptic, disinfectant, and local irritant effects when applied externally. Ethanol coagulates proteins and is active against gram-positive and gram-negative bacteria as well as viruses.

Pharmacokinetics.

Not absorbed through the skin when applied locally.

Clinical characteristics.

Indications.

Furuncles, panaritium, infiltrates, mastitis in the initial stages.

For wiping and compresses. For surgical hand disinfection.

Contraindications.

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

Safety precautions.

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

Avoid contact of the preparation with eyes!

Interaction with other medicinal products and other forms of interaction.

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

Special precautions.

Use during pregnancy or breastfeeding.

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

Ability to influence the reaction rate while driving or operating machinery.

No effect.

Administration and Dosage.

For external use only — for wiping, compresses, and disinfection of the skin, including hands.

For compresses and wiping (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.

When applied locally, skin or mucous membrane irritation is possible.

If any adverse reactions occur, consult a physician.

Shelf life.

5 years.

The 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, away from fire.

Keep out of reach of children.

Packaging. 100 ml in bottles.

Prescription status. Prescription only.

Manufacturer: JSC "FITOPHARM".

Manufacturer's address and location of business activity:

2 Sybirtseva Street, Bakhmut, Donetsk region, 84500, Ukraine.

Marketing Authorization Holder: JSC "FITOPHARM".

Address of the Marketing Authorization Holder:

7, Verkhovnoyi Rady Avenue, Premises 18, 3rd floor, Kyiv, 02100, Ukraine.