HEVACAMEN
UkraineThe drug is used for the symptomatic treatment of neuralgia, myalgia, arthritis, rheumatism, and sciatica.
Frequently asked questions
How should Hevacamen ointment be used correctly?
Apply 2-3 g of the ointment to the affected area of the body and the surrounding skin, rubbing it in until fully absorbed, 2-3 times daily. Hands should be washed thoroughly after each application.
What are the possible side effects of Hevacamen?
Possible allergic reactions include: redness, rash, urticaria, itching, or contact dermatitis. Headache, dizziness, or convulsions may also occur (due to the camphor content).
Who should not use this drug?
Contraindicated in cases of hypersensitivity to the components, presence of wounds, dermatitis, or eczema at the application site, as well as in cases of pertussis, predisposition to convulsions, or bronchospasm. Not recommended for pregnant women, breastfeeding women, and children under 12 years of age.
Can the ointment be applied to damaged skin or mucous membranes?
No, the ointment must not be applied to damaged skin or mucous membranes, and must not come into contact with the eyes. In case of contact with the eyes, rinse them immediately with water and consult a physician.
What sensations may occur during application?
Upon application, a sensation of cold is initially felt, followed by warmth, mild burning, and tingling.
Instructions for use
I N S T R U C T I O N for medical use of the medicinal product GHEVKAMEN
Composition:
Active substances: menthol crystals, racemic camphor, eucalyptus oil, clove oil;
1 g of ointment contains: menthol crystals 0.18 g; racemic camphor 0.10 g; eucalyptus oil 0.10 g; clove oil 0.01 g;
Excipients: paraffin, white soft paraffin.
Pharmaceutical form. Ointment.
Main physicochemical characteristics: ointment of white or white with a yellowish tint color and characteristic odor.
Pharmacotherapeutic group.
Agents applied locally for joint and muscular pain.
ATC code M02A X10.
Pharmacological properties.
Pharmacodynamics.
The ointment stimulates nerve endings, producing a counterirritant, local analgesic, and anti-inflammatory effect, which is caused by the substances contained in its composition.
Pharmacokin游戏副本ics.
Pharmacokinetics has not been determined.
Clinical characteristics.
Indications.
Symptomatic treatment of neuralgia, myalgia, arthritis, rheumatism, and sciatica.
Contraindications.
Hypersensitivity to any component of the drug. Wounds at the site of application, dermatitis, whooping cough, eczema, predisposition to bronchospasm or seizures.
Safety precautions.
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 cold, followed by warmth, mild burning, and tingling.
Do not apply the ointment to damaged skin.
Hands should be washed thoroughly after each application.
If strong skin irritation occurs, discontinue rubbing in the ointment.
Interaction with other medicinal products and other forms of interaction. Unknown.
Usage Notes.
Use during pregnancy or breastfeeding.
Do not use during pregnancy or breastfeeding.
Ability to affect reaction speed when driving or operating machinery.
Unknown.
Method of Administration and Dosage.
Apply the ointment externally by rubbing it in.
Apply 2–3 g of the preparation 2–3 times daily, gently rubbing it into the affected area and adjacent skin until completely absorbed.
The frequency of application and duration of treatment are determined by the physician depending on the nature of the disease, its severity, the therapeutic effect achieved, and the characteristics of the underlying therapy.
Children.
Not recommended for children under 12 years of age.
Overdose.
Sensation of intense warmth and burning at the application site or worsening of adverse reactions. Allergic reactions (urticaria, skin itching) in cases of hypersensitivity to the drug. Symptomatic treatment is recommended.
Side effects.
Allergic reactions are possible, including skin redness, skin rash, urticaria, contact dermatitis, itching; headache, dizziness, possible seizures caused by camphor; dermatitis may occur in children.
Shelf life. 3 years.
Storage conditions.
Store in the original packaging at a temperature not exceeding 25 °C; do not freeze. Keep out of reach of children.
Packaging.
20 g, 30 g, or 40 g in aluminum or laminated tubes, 1 tube per carton or without carton; 20 g or 40 g in containers.
Dispensing category. Over-the-counter (without prescription).
Manufacturer. JSC Pharmaceutical Factory "Viola".
Manufacturer's address and place of business.
75 Amosova Akademika Street, Zaporizhzhia, 69063, Ukraine.
Marketing authorization holder. JSC Pharmaceutical Factory "Viola".
Address of the marketing authorization holder.
75 Amosova Akademika Street, Zaporizhzhia, 69063, Ukraine.
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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