Formic alcohol

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

Composition:

Active substance: formic acid;

100 ml of the preparation contain 1.4 g of formic acid;

Excipient: ethanol 70%.

Pharmaceutical form. Alcoholic solution for external use.

Main physico-chemical properties: clear, colorless liquid with a specific pungent odor.

Pharmacotherapeutic group.

Agents used locally for joint and muscular pain.

ATC code M02AX10.

Pharmacological properties.

Formic alcohol belongs to agents that stimulate sensory nerve endings. Due to stimulation of skin and subcutaneous tissue receptors, the drug exerts not only a reflexive but also a general humoral effect. Stimulation of receptors by Formic alcohol is accompanied by enhanced formation and release of endorphins, dynorphins, and peptides that play an important role in regulation of pain sensations, vascular permeability, and other processes.

Clinical characteristics.

Indications.

Neuralgias, myositis, arthralgias.

Contraindications.

Hypersensitivity to the drug. Eczema, inflammatory and infectious skin diseases localized in the area of application, as well as allergic diseases.

Special precautions.

Avoid contact of the drug with mucous membranes and eyes.

Do not violate the instructions for use of the medicinal product, as this may harm health.

Interaction with other medicinal products and other forms of interaction.

When used simultaneously with preparations containing organic compounds, new compounds may form, as well as denaturation of protein components.

When using any other medicinal products concurrently, inform your doctor.

Special precautions.

Use during pregnancy or breastfeeding.

The use of the drug during pregnancy or breastfeeding is possible only when the expected benefit to the mother outweighs the potential risk to the fetus or child.

Ability to influence reaction rate when driving or operating machinery.

Does not affect.

Administration and dosage.

Apply formic alcohol externally by rubbing it into the affected area of the skin. The frequency of application and duration of treatment are determined by the nature and severity of the disease.

Children.

Not recommended for children under 12 years of age.

Overdose.

Not observed.

Side effects.

Possible severe skin irritation, rashes, blister formation.

If any adverse reactions occur, consult a physician immediately!

Shelf life. 3 years.

Do not use the medicinal product after the expiry date stated on the package.

Storage conditions. Store in the original packaging at a temperature not exceeding 25°C. Keep out of reach of children.

Packaging. 40 ml or 50 ml in vials.

Availability. Over-the-counter (without prescription).

Manufacturer. JSC Pharmaceutical Factory "Viola".

Manufacturer's name and address.

69063, Ukraine, Zaporizhzhia, Amosova St., 75.

Marketing Authorization Holder. JSC Pharmaceutical Factory "Viola".

Address of the Marketing Authorization Holder.

69063, Ukraine, Zaporizhzhia, Amosova St., 75.