HEVACAMEN
UkraineThe drug is used for the symptomatic treatment of neuralgia, myalgia, arthritis, rheumatism, and sciatica.
Frequently asked questions
How should Hevacamen be used correctly?
The ointment should be rubbed into the affected area of the body and the surrounding skin until fully absorbed. It is recommended to use 2–3 g of the product 2–3 times a day.
What side effects can Hevacamen cause?
Possible allergic reactions include: redness, rash, urticaria, itching, or contact dermatitis. Headache, dizziness, or convulsions (due to camphor) may also occur.
Who should not use this drug?
The product should not be used in case of hypersensitivity to the components, presence of wounds, eczema, or dermatitis at the application site, as well as in cases of whooping cough or a tendency toward convulsions or bronchospasm.
Can the ointment be used by children?
Use of this product is not recommended for children under 12 years of age.
What should be done if the ointment gets into the eyes?
The eyes must be rinsed immediately with water, and medical attention should be sought urgently.
What sensations occur during application?
When rubbed into the skin, a sensation of cold is initially felt, followed by warmth, mild burning, and tingling.
Can the drug be used by pregnant or breastfeeding women?
A doctor may prescribe treatment in cases where the expected benefit to the woman outweighs the potential risk to the child or fetus.
Instructions for use
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
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The original data is available in the language of the country of manufacture.
Data source: State Register of Medicinal Products of Ukraine
Data last verified: August 13, 2026