Camphor spirit

Ukraine
Brand name Camphor spirit
Form solution, alcoholic, for external use
Active substance / Dosage
racemic camphor · 10 g/100 ml
Prescription type over-the-counter (OTC)
ATC code
Registration number UA/7967/01/01
Manufacturer PJSC "Fitofarm"
Camphor spirit solution, alcoholic, for external use

INSTRUCTION FOR MEDICAL USE OF THE MEDICINAL PRODUCT CAMPHOR SPIRIT

Composition:

Active ingredient: racemic camphor;

100 ml of solution contain 10 g of racemic camphor;

Excipient: 70% ethanol.

Pharmaceutical form. 10% alcoholic solution for external use.

Main physicochemical properties: clear colorless liquid with a characteristic camphor odor.

Pharmacotherapeutic group.

Topical preparations used for joint and muscular pain.

ATC code M02AX10.

Pharmacological properties.

The drug exerts antimicrobial, analgesic, anti-inflammatory, and irritant effects.

Clinical characteristics.

Indications. Topical use — for inflammatory conditions (arthritis, myositis, arthralgia, myalgia, sciatica), prevention of pressure ulcers.

Contraindications. Hypersensitivity. Skin ulcerative-necrotic disorders, predisposition to convulsive reactions.

Special precautions.

Avoid contact of the drug with eyes.

Avoid contact of the drug with mucous membranes. In case of accidental contact, rinse thoroughly with large amounts of running water.

Do not violate the application instructions of the medicinal product, as this may harm health.

Interaction with other medicinal products and other types of interactions. Not observed.

Special precautions for use.

Use during pregnancy or breastfeeding.

During pregnancy and breastfeeding, the drug should be used only if the expected benefit for the mother outweighs the potential risk to the fetus or infant.

Ability to affect reaction speed when driving or operating machinery. No effect.

Method of Administration and Dosage.

Camphor alcohol is used externally in adults for rubbing in the indicated pathological conditions. Apply to the skin 2–3 times daily.

The duration of treatment is determined individually.

Children. Not to be used in children under 12 years of age.

Overdose. Increased incidence of adverse reactions. Treatment is symptomatic.

Adverse reactions.

Possible manifestations of allergic reactions, rashes, urticaria, skin irritation, headache, dizziness.

If any adverse events occur, consult a physician immediately!

Shelf life. 5 years.

The product must not be used after the expiry date stated on the package.

Storage conditions.

Store in the original packaging at a temperature not exceeding 25 °C.

Keep out of reach of children.

Packaging. 40 ml in bottles.

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

Manufacturer. JSC "FITOFARM".

Manufacturer's address and location of business activity.

2 Sybirtseva St., Bakhmut, Donetsk region, 84500, Ukraine.

Marketing Authorization Holder. JSC "FITOFARM".

Address of the Marketing Authorization Holder.

12 Almatinska St., Kyiv, 02092, Ukraine.