Formidron

I N S T R U C T I O N for medical use of the medicinal product FORMIDRON

Composition:

Active substances: formaldehyde, ethanol;

100 ml of solution contain formaldehyde solution equivalent to 35 % formaldehyde content - 10.0 g, 96 % ethanol - 39.5 g;

Excipients: eau de cologne, purified water.

Pharmaceutical form. Solution for external use.

Main physicochemical properties: transparent, colorless liquid with an aromatic odor.

Pharmacotherapeutic group.

Dermatological preparations. Agents used in hyperhidrosis.

ATC code D11A A.

Pharmacological properties.

The drug exerts disinfectant and deodorizing effects.

Clinical characteristics.

Indications.

Formidron is used for skin treatment in cases of increased sweating.

Contraindications.

Hypersensitivity to the components of the drug. Skin diseases. Children under 14 years of age.

Special precautions.

Should be used with caution in elderly patients and during pregnancy. Do not apply to the face to avoid irritation. Avoid contact with eyes and mucous membranes.

The recommended usage instructions for the medicinal product must not be violated, as this may harm health.

Interaction with other medicinal products and other types of interactions.

Not described.

Special precautions for use.

Redness and itching of the skin immediately after application of the drug indicate individual hypersensitivity and require immediate discontinuation of the drug.

Use during pregnancy or breastfeeding.

During pregnancy and breastfeeding, the drug may be used only if the expected benefit to the mother outweighs the potential risk to the fetus or infant.

Ability to affect reaction speed when driving or operating machinery.

Does not affect.

Dosage and Administration.

For external use only. Adults and children over 14 years of age should wipe the skin with a cotton swab moistened with the medication 1–2 times daily.

Children.

Not recommended for children under 14 years of age.

Overdose.

Overdose should be avoided. With prolonged and frequent use, if redness, itching, or irritation occurs—signs of overdose—treatment with the medication must be discontinued. Wash the medication off the skin with water. Symptomatic therapy should be administered.

Side effects.

Skin irritation, allergic reactions, sensation of itching.

If any adverse events occur, consult a physician!

Shelf life. 4 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. Keep out of reach of children.

Packaging.

50 ml in glass bottles. 50 ml in polymer bottles, in a carton or without a carton. 100 ml in glass or polymer bottles, in a carton or without a carton. 100 ml in polymer bottles with a mechanical spray pump.

Supply category. Over-the-counter (without prescription).

Manufacturer. JSC Pharmaceutical Factory "Viola".

Manufacturer's address and place of business.

75 Amosova Akademika Street, Zaporizhzhia, 69063, Ukraine.

Marketing authorization holder. JSC Pharmaceutical Factory "Viola".

Address of the marketing authorization holder.

75 Amosova Akademika Street, Zaporizhzhia, 69063, Ukraine.