Perkamf (Solution) Instructions for Use

Marketing Authorization Holder

Yaroslavl Pharmaceutical Factory, CJSC (Russia)

ATC Code

M02AB (Capsaicin and similar agents)

Active Substances

Camphor (Ph.Eur. European Pharmacopoeia)

Capsicum (Rec.INN WHO registered)

Dosage Form

Perkamf

Topical alcoholic solution: 100 ml bottle or dropper bottle

Dosage Form, Packaging, and Composition

Topical alcoholic solution – a transparent reddish-brown liquid with a characteristic camphor odor.

100 ml – bottle (1) – cardboard packs.
100 ml – dropper bottle (1) – cardboard packs.
100 ml – bottle (9-300) – group packaging (for hospitals).
100 ml – dropper bottle (9-300) – group packaging (for hospitals).

Clinical-Pharmacological Group

Drug with anti-inflammatory and analgesic action for external use

Pharmacotherapeutic Group

Local irritant of plant origin

Pharmacological Action

A combined topical agent of plant origin. It has a local irritant, anti-inflammatory, and analgesic effect.

Indications

• Neuralgia
• Radiculopathy
• Myalgia
• Lumbago
• Lumbosciatica

Apply externally for symptomatic relief of pain associated with these musculoskeletal and nervous system conditions.

ICD codes

Dosage Regimen

Apply externally by rubbing into the affected skin area 2-3 times daily.

Use a sufficient amount to cover the painful area. Duration of use depends on symptom severity and should not exceed 10-14 days without medical consultation.

Avoid application to large body surface areas. Do not apply under occlusive dressings or tight bandages.

Adverse Reactions

At the application site: severe burning, erythema, skin irritation, pruritus, or allergic contact dermatitis.

Systemic reactions are unlikely with proper topical use but may occur with excessive application or on damaged skin.

Discontinue use immediately and consult a physician if severe skin reactions develop.

Drug Interactions

No specific drug interaction studies have been conducted.

Concurrent use with other topical products on the same skin area may increase skin irritation or systemic absorption.

Avoid applying other topical medications, especially those with irritant or drying effects, to the same treatment area.

Contraindications

• Hypersensitivity to camphor, capsicum, or any component of the formulation.
• Application to damaged skin, including wounds, abrasions, eczema, or dermatitis.
• Use on mucous membranes or near the eyes.

Do not use in children under 12 years of age. Contraindicated in patients with known allergy to plants of the Solanaceae family.

Overdose

Symptoms of topical overdose include severe skin irritation, burning sensation, erythema, or blistering.

Accidental ingestion may cause gastrointestinal irritation, nausea, vomiting, abdominal pain, dizziness, or headache.

In case of accidental ingestion, seek immediate medical attention. For topical overdose, wash the area thoroughly with soap and water.

Storage Conditions

Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

Dispensing Status

Over-the-Counter

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.