Hevacamen

INSTRUCTION FOR MEDICAL USE OF THE MEDICINAL PRODUCT GHEVCAMEN (Gevcamen)

Composition:

Active substances: 1 g of ointment contains menthol – 0.18 g; racemic camphor – 0.1 g; eucalyptus oil – 0.1 g; clove oil – 0.01 g;

Excipients: paraffin, white soft paraffin.

Pharmaceutical form. Ointment.

Main physicochemical properties: ointment of white or whitish-yellowish color, with a characteristic odor.

Pharmacotherapeutic group.

Agents used locally for joint and muscular pain.

ATC code M02A X10.

Pharmacological properties.

Pharmacodynamics. When applied externally, the medicinal product stimulates the nerve endings of the skin and exerts a counterirritant, local analgesic, anti-inflammatory, and antimicrobial effect in inflammation, joint pain, and muscle pain.

Pharmacokinetics. Not studied.

Clinical characteristics.

Indications.

Symptomatic treatment of neuralgia, myalgia, arthritis, rheumatism, and sciatica.

Contraindications.

Hypersensitivity to any of the components of the drug. Skin lesions at the site of application, dermatitis, whooping cough, eczema, predisposition to bronchospasm or seizures.

Interaction with other medicinal products and other forms of interaction.

Unknown.

Special precautions for use.

Caution should be exercised when applying the ointment.

Do not apply to mucous membranes! Avoid contact with eyes. In case of accidental contact with eyes, rinse thoroughly with water and seek medical advice immediately.

When rubbed into the skin, may cause a sensation of coldness, followed by warmth, mild burning, and tingling.

Do not apply the ointment to damaged skin.

Hands should be thoroughly washed after each application.

If strong skin irritation occurs, discontinue rubbing in the ointment.

Use during pregnancy or breastfeeding.

During pregnancy and breastfeeding, treatment should be prescribed by a physician only when the expected benefit to the woman outweighs the potential risk to the fetus/infant.

Ability to affect reaction speed when driving or operating machinery.

No effect.

Method of Administration and Dosage.

Apply the ointment externally for rubbing in.

Gently rub 2–3 g of the preparation into the affected area and adjacent skin until completely absorbed, 2–3 times daily.

The frequency of application and duration of treatment course are determined by a physician depending on the nature and severity of the disease, therapeutic response achieved, and characteristics of the underlying therapy.

Children.

The medicinal product is not recommended for children under 12 years of age.

Overdose.

Sensation of intense warmth and burning at the application site or exacerbation of adverse reactions. Allergic reactions (urticaria, skin itching) in case of hypersensitivity to the drug. Treatment is symptomatic.

Side effects.

Allergic reactions are possible, including skin redness, skin rashes, urticaria, contact dermatitis, itching; headache, dizziness, possible seizures caused by camphor; dermatitis may occur in children.

Shelf life. 3 years.

Storage conditions.

Store in original packaging at a temperature not exceeding 25 ºС.

Keep out of reach of children.

Packaging.

15 g or 25 g in aluminium tubes, in a carton or without carton.

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

Manufacturer/Applicant.

LLC "Ternopharm".

Manufacturer's address / Applicant's address.

LLC "Ternopharm".

46010, Ternopil, Fabrychna St., 4, Ukraine.

Tel./Fax: (0352) 521-444, www.ternopharm.com.ua