Hevacamen
Ukraine
Table of Contents
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.