Camphor oil for external use 10% bottle 30 ml

Instructions Camphor oil for external use 10% bottle 30 ml

Composition

active ingredient: racemic camphor;

1 ml of the drug contains 0.1 g of racemic camphor;

excipient: sunflower oil.

Dosage form

Oil for external use.

Basic physicochemical properties.

Clear yellow liquid with a camphor odor.

Pharmacotherapeutic group

Topical agents for joint and muscle pain.

ATX code M02A X10.

Pharmacological properties

Pharmacodynamics.

Camphor oil, when applied topically, has antimicrobial, anti-inflammatory, distracting, analgesic effects, and eliminates skin itching.

These properties are due to the presence in the camphor molecule of a functionally active oxygen molecule, which has a high oxidizing potential, disrupts the cell membranes of microorganisms, and destroys many active compounds that cause inflammation, pain, and irritation of sensitive skin receptors.

Pharmacokinetics.

Pharmacokinetics have not been determined.

Indication

It is prescribed for rheumatism, arthritis, arthralgia, myositis, sciatica, and skin itching.

Contraindication

Increased individual sensitivity to the components of the drug. Bronchial asthma, skin damage due to burns, impaired skin integrity, pustular skin diseases.

Special safety precautions

For external use only. Avoid contact with eyes, mucous membranes and open wounds. Do not rub into nostrils. In rare cases, allergic reactions are possible. If such reactions occur, discontinue use of the drug and wash off any residue from the application site with warm water and soap.

Interaction with other medicinal products and other types of interactions

The interaction is not yet known.

Use during pregnancy or breastfeeding

It is used taking into account the benefit-risk ratio for the woman/fetus (child), which is determined by the doctor.

Ability to influence reaction speed when driving vehicles or other mechanisms

Not studied.

Method of administration and doses

Camphor oil is used externally by adults both separately and in combination with methyl salicylate, turpentine and other drugs for local use. It is used externally for rubbing and compresses in the indicated pathological processes. The method of application, the number of applications, the duration of one application are determined by the nature of the disease, its severity, and the nature of concomitant therapy.

Children

Not used in children due to lack of clinical experience.

Overdose

Possible increased manifestations of adverse reactions, a feeling of intense heat and burning.

Accidental ingestion may cause abdominal pain, nausea, vomiting, diarrhea, symptoms of central nervous system depression, dizziness, ataxia, convulsions, hot flashes, drowsiness, and difficulty breathing.

Side effects

Skin: allergic reactions, including skin rash, urticaria, itching, skin irritation, redness, dermatitis, including contact dermatitis.

Nervous system: convulsions.

Respiratory system: bronchospasm.

Expiration date

2 years.

Storage conditions

Store in original packaging at a temperature not exceeding 25 ° C. Keep out of the reach of children.

Packaging

30 ml in glass or polymer bottles in a pack or without a pack.

Vacation category

Without a prescription.

Producer

PrJSC Pharmaceutical Factory "Viola".

Location of the manufacturer and its business address.

69063, Ukraine, Zaporizhia, Akademika Amosova St., 75.

Applicant

PrJSC Pharmaceutical Factory "Viola".

Location of the applicant.

69063, Ukraine, Zaporizhia, Akademika Amosova St., 75.