Iodine

INSTRUCTIONS FOR MEDICAL USE OF THE MEDICINAL PRODUCT IODINE (IODINE)

Composition:

Active ingredient: iodine;

1 ml of solution contains: iodine – 0.05 g;

Excipients: potassium iodide, ethanol 96%, purified water.

Pharmaceutical form. Topical solution, alcoholic.

Main physicochemical properties: red-brown transparent liquid in a thin layer, with a characteristic odor.

Pharmacotherapeutic group. Antiseptics and disinfectants.

ATC code D08AG03.

Pharmacological properties.

Pharmacodynamics.

The drug contains elemental iodine, which has antimicrobial, local irritant, and counterirritant effects. When applied to the skin and mucous membranes, the drug exerts an irritant effect and may cause reflex changes in body functions. Iodine penetrates and actively influences metabolism, enhancing dissimilation processes.

Pharmacokinetics.

Not studied.

Clinical characteristics.

Indications.

Used externally as an antiseptic and irritant agent in infectious and inflammatory diseases of the skin and mucous membranes, for surgical site preparation, for prevention of infection in minor skin injuries, and for reduction of inflammatory processes in myositis and neuralgia (exerts a distracting effect).

Contraindications.

Hypersensitivity to iodine. The drug is also contraindicated in diabetic and trophic ulcers.

Interaction with other medicinal products and other forms of interaction.

When used simultaneously with topical agents containing organic compounds, denaturation of protein components may occur.

Incompatible with essential oils, ammonia solution, and brilliant green. Incompatible with disinfectant medicinal products containing mercury compounds, alkalis, and reducing agents.

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

Special precautions for use.

Caution should be exercised when applying iodine to mucous membranes, as the alcohol contained in the preparation may cause burns and severe irritation. Avoid contact of the preparation with the eyes. Particular caution should be exercised when using iodine in patients with light hair.

Should not be applied to large skin areas due to the risk of developing burns.

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

Use during pregnancy or breastfeeding.

The use of the preparation during pregnancy and breastfeeding is not recommended due to the possible risk of developing thyroid dysfunction in the fetus/child.

Ability to affect reaction speed while driving or operating machinery.

No effect.

Method of Administration and Dosage.

For external use, iodine is used to moisten a cotton swab, which is then applied to treat affected areas of the skin.

Children. Do not use in newborns due to the possible risk of thyroid dysfunction and skin lesions.

Overdose.

In case of overdose, symptoms of iodism may occur (rhinitis, urticaria, Quincke's edema, lacrimation, salivation, acne-like skin eruptions), as well as burns and skin irritation.

Treatment is symptomatic.

Adverse reactions.

Possible occurrence of rhinitis, urticaria, Quincke's edema, hypersalivation and lacrimation, skin rashes, contact dermatitis.

In case of any adverse events, it is necessary to consult a physician.

Shelf life: 3 years.

Do not use after the expiry date stated on the packaging.

Storage conditions:

Store in a light-protected place at a temperature not exceeding 25 °C.

Keep out of reach of children.

Packaging:

10 mL, or 20 mL, or 1000 mL in bottles.

Dispensing category:

Over-the-counter (without prescription).

Manufacturer:

JSC "CHEMICAL PHARMACEUTICAL PLANT "CHERVONA ZIRKA".

Manufacturer's address and location of business activity:

1 Gordienkivska Street, Kharkiv, Kharkiv Oblast, 61010, Ukraine.