Korychka

INSTRUCTIONS FOR MEDICAL USE OF THE MEDICINAL PRODUCT CINNAMON

Composition:

Active substance: cinnamon bark tincture;

1 vial contains cinnamon bark tincture (Cinnamomi cortex) (1:5) (extraction solvent — 70% ethanol) 50 ml or 100 ml.

Pharmaceutical form. Tincture.

Main physico-chemical properties: clear, reddish-brown liquid with a characteristic odor.

Pharmacotherapeutic group. Other agents used in functional gastrointestinal disorders. ATC code A03A X.

Pharmacological properties.

Pharmacodynamics.

Cinnamon tincture is a medicinal product used for gastrointestinal functional disorders. The effect of the medicinal product is determined by biologically active substances contained in its composition.

Pharmacokinetics.

Not studied.

Clinical characteristics.

Indications.

For symptomatic treatment of mild, spasmodic gastrointestinal disorders, including bloating and flatulence.

Contraindications.

• Hypersensitivity to any component of the medicinal product and to Peru balsam;
• gastric and duodenal ulcer;
• fever of unknown origin;
• pregnancy and breastfeeding period;
• patient age under 18 years.

Interaction with other medicinal products and other forms of interaction.

Interaction with other medicinal products is not known.

Special precautions for use

The medicinal product should be taken orally.

Cinnamon is a traditional herbal medicinal product used according to indications supported exclusively by long-standing use.

The patient should consult a physician if symptoms persist for more than 2 weeks during use of the medicinal product or if adverse reactions occur that are not listed in the product's instructions for medical use.

This medicinal product contains 70% v/v ethanol (alcohol), i.e. 742 mg/dose, equivalent to 19 ml of beer or 8 ml of wine per dose.

Harmful for patients suffering from alcoholism. Caution is advised when administering to patients with liver disorders and in patients with epilepsy.

Use during pregnancy or breastfeeding

The medicinal product is contraindicated during pregnancy and breastfeeding.

Ability to affect reaction rate while driving or operating machinery

The medicinal product contains ethanol and may cause drowsiness; therefore, during treatment, it is not recommended to engage in activities requiring high attention, or rapid mental and motor reactions.

Method of Administration and Dosage.

Take orally after meals. The recommended dose for adults is 2–4 ml per day, divided into three doses, diluted in ½ glass of water.

The patient should consult a physician if symptoms persist for more than 2 weeks during medication use or if adverse reactions occur that are not listed in the instructions for medical use of the drug.

Children.

Do not use in children and adolescents under 18 years of age.

Overdose.

Information on overdose is not available.

Side effects.

Allergic reactions are possible. Gastrointestinal disturbances may occur with prolonged use.

If any adverse symptoms occur, discontinue use of the medicinal product and seek immediate medical advice.

Shelf life. 3 years.

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

Packaging. 50 ml or 100 ml in bottles.

Supply category. Over-the-counter.

Manufacturer.

LLC "DKP "Pharmaceutical Factory".

Manufacturer's address and place of business.

4, Korolyova St., Stanishivka, Zhytomyr district, Zhytomyr region, 12430, Ukraine.