Dolgitblok (Gel) Instructions for Use

Marketing Authorization Holder

Dolorgiet, GmbH & Co. KG (Germany)

ATC Code

M02AA13 (Ibuprofen)

Active Substances

Ibuprofen (Rec.INN registered by WHO)

Levomenthol (Rec.INN registered by WHO)

Dosage Form

Dolgitblok

Gel for external use 5%+3%

Dosage Form, Packaging, and Composition

Gel for external use

100 g – tubes – cardboard packs – Over-the-Counter
150 g – tubes – cardboard packs – Over-the-Counter
20 g – tubes – cardboard packs – Over-the-Counter
50 g – tubes – cardboard packs – Over-the-Counter

Clinical-Pharmacological Group

NSAIDs for external use

Pharmacotherapeutic Group

Drugs for external use for muscle and joint pain; non-steroidal anti-inflammatory drugs for external use

Pharmacological Action

Ibuprofen non-selectively blocks COX-1 and COX-2 enzymes, thereby suppressing the synthesis of prostaglandins – mediators of pain, inflammation, and hyperthermic reaction.

When applied topically, it has an analgesic and anti-inflammatory effect.

Levomenthol has a local irritant effect.

This combination reduces pain and inflammation, is effective for joint pain during movement and at rest, and reduces morning joint stiffness.

Pharmacokinetics

After application to the skin, Ibuprofen is detected in the epidermis and dermis within 24 hours.

It reaches a high therapeutic concentration in the underlying soft tissues, joints, and synovial fluid.

Clinically significant systemic absorption is practically absent.

C_max in blood plasma with topical application is 5% of the C_max level with oral administration.

Ibuprofen undergoes metabolism in the liver.

It is excreted by the kidneys (unchanged no more than 1%) and, to a lesser extent, with bile through the intestines.

Indications

Muscle pain, back pain, arthritis, pain from ligament damage and sprains, sports injuries, and neuralgia.

ICD codes

Dosage Regimen

Apply externally only. Use a thin layer on the affected skin area.

Administer the gel and gently rub in until fully absorbed.

Apply up to four times within a 24-hour period.

Maintain an interval of at least four hours between applications.

The standard treatment duration is up to 10 days.

Do not exceed the recommended daily frequency or total duration of use.

For adults and adolescents 14 years of age and older.

Wash hands thoroughly with soap and water after each application.

Discontinue use and consult a physician if symptoms persist or worsen.

Adverse Reactions

From the immune system hypersensitivity reactions (non-specific allergic reactions and anaphylactic reactions).

From the respiratory system: bronchial asthma, including its exacerbation, bronchospasm, shortness of breath, dyspnea.

From the skin: itching, urticaria, purpura, exfoliative and bullous dermatoses, including toxic epidermal necrolysis (Lyell’s syndrome), Stevens-Johnson syndrome, erythema multiforme, eczema, photosensitivity, angioedema.

From the gastrointestinal tract abdominal pain, dyspepsia.

From the kidneys and urinary tract impaired renal function.

Contraindications

Hypersensitivity to ibuprofen, acetylsalicylic acid and other NSAIDs, complete or incomplete combination of bronchial asthma, recurrent nasal and sinus polyposis and intolerance to acetylsalicylic acid or other NSAIDs, impaired skin integrity at the application site, children under 14 years of age, pregnancy, lactation period.

Use in Pregnancy and Lactation

Use is contraindicated during pregnancy and lactation.

Pediatric Use

Use is contraindicated in children under 14 years of age.

Special Precautions

Avoid contact with eyes, lips and other mucous membranes, and damaged skin areas.

After application to the skin, an occlusive dressing should not be applied.

Drug Interactions

This combination may enhance the effect of drugs that increase photosensitivity.

Since even with topical use of ibuprofen, the possibility of systemic action cannot be completely excluded, caution should be exercised when used concomitantly with the following drugs: anticoagulants and thrombolytic drugs, antihypertensive agents, acetylsalicylic acid, other NSAIDs.

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.