Terebinthin oil (Ointment) Instructions for Use

Marketing Authorization Holder

Yaroslavl Pharmaceutical Factory, CJSC (Russia)

ATC Code

N02 (Analgesics)

Active Substance

Turpentine oil (BP British Pharmacopoeia)

Dosage Form

Turpentine oil

Ointment for external use 20%: jar 100 ml

Dosage Form, Packaging, and Composition

100 ml – dark glass jars (1) – cardboard packs.

Clinical-Pharmacological Group

Drug with local irritant and analgesic action

Pharmacotherapeutic Group

Local irritant of plant origin

Pharmacological Action

A natural origin agent that has a local irritant, analgesic, “distracting” and antiseptic effect.

Indications

• Use as part of complex therapy for neuralgia and myalgia.
• Apply for rheumatic pains and lumbosciatica to alleviate discomfort.

ICD codes

Dosage Regimen

Apply externally to the affected areas. Use a sufficient amount to cover the skin and rub in with light circular motions for several minutes until fully absorbed.

Repeat application 1 to 3 times per day, depending on the severity of symptoms. Avoid use on damaged skin, mucous membranes, or open wounds. Wash hands thoroughly after application.

Adverse Reactions

Local skin reactions, including redness, itching, burning sensation, or urticaria, may occur at the application site.

In cases of hypersensitivity, more severe allergic reactions, such as skin rash or dermatitis, are possible. Discontinue use immediately if any adverse reactions develop.

Drug Interactions

No specific drug interactions are currently known. The potential for interaction with other topically applied products exists.

Avoid concurrent application with other local irritants or topical medications on the same skin area to prevent additive skin irritation or unpredictable effects.

Contraindications

• Do not use in case of known hypersensitivity to turpentine oil or any other component of the ointment.
• Contraindicated for application on damaged skin, eczematous skin, or mucous membranes.
• Avoid use in patients with severe hepatic impairment or severe renal impairment due to potential systemic absorption.

Overdose

Symptoms of overdose include intense skin irritation, severe redness, burning pain, or blister formation.

In case of accidental ingestion, seek immediate medical attention. Treatment is symptomatic and supportive. For dermal overdose, thoroughly wash the affected area with soap and water and do not reapply the product.

Use in Hepatic Impairment

With caution: hepatic impairment.

Use in Renal Impairment

With caution: renal impairment.

Storage Conditions

The drug should be stored at a temperature not exceeding 25°C (77°F), in a place protected from light and out of the reach of children.

Shelf Life

Shelf life – 5 years. Do not use after the expiration date printed on the packaging.

Dispensing Status

The drug is approved for use as an over-the-counter product.

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.