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Next Activgel (Gel) Instructions for Use

Marketing Authorization Holder

Otisipharm, JSC (Russia)

Manufactured By

Lekko, CJS (Russia)

ATC Code

M02AA13 (Ibuprofen)

Active Substances

Ibuprofen (Rec.INN WHO registered)

Levomenthol (Rec.INN WHO registered)

Dosage Form

Bottle OTC Icon Next Activgel Gel for external use 50 mg+30 mg/1 g: 25 g, 50 g, or 100 g tubes

Dosage Form, Packaging, and Composition

Gel for external use transparent, colorless or grayish-pinkish, or yellowish in color, with a menthol odor; the presence of opalescence and air bubbles is allowed.

1 g
Ibuprofen 50 mg
Levomenthol 30 mg

Excipients: propylene glycol – 100 mg, ethanol 95% – 300 mg, carbomer – 20 mg, diisopropanolamine – 55 mg, purified water – up to 1000 mg.

25 g – tubes (1) – cardboard packs.
50 g – tubes (1) – cardboard packs.
100 g – tubes (1) – cardboard packs.

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 the enzymes COX-1 and COX-2, 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 after 24 hours. It reaches a high therapeutic concentration in the underlying soft tissues, joints, and synovial fluid. Clinically significant systemic absorption practically does not occur. Cmax in blood plasma with topical application is 5% of the Cmax 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

ICD-10 code Indication
M05 Seropositive rheumatoid arthritis
M13.8 Other specified arthritis
M15 Polyosteoarthritis
M25.5 Pain in joint
M54 Dorsalgia
M54.1 Radiculopathy
M54.3 Sciatica
M54.4 Lumbago with sciatica
M79.1 Myalgia
M79.2 Neuralgia and neuritis, unspecified
T14.3 Dislocation, sprain and strain of joint and ligament of unspecified body region
ICD-11 code Indication
8B93.Z Radiculopathy, unspecified
8E4A.1 Paraneoplastic or autoimmune diseases of the peripheral or autonomic nervous system
FA05 Polyosteoarthritis
FA20.0 Seropositive rheumatoid arthritis
FA2Z Inflammatory arthropathies, unspecified
FB56 Specified soft tissue diseases, not elsewhere classified
FB56.2 Myalgia
ME82 Pain in joint
ME84.20 Lumbago with sciatica
ME84.3 Sciatica
ME84.Z Back pain, unspecified
ND56.3 Dislocation, sprain or strain of unspecified body region

Dosage Regimen

The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen.

Apply the gel externally to intact skin only.

Use a thin layer, 3 to 5 cm (1-2 inches) per application, depending on the size of the affected area.

Gently massage the gel into the skin until fully absorbed.

Apply the gel up to 4 times within a 24-hour period.

Maintain a minimum interval of 4 hours between applications.

The maximum duration of continuous use is 10 days.

If no improvement is observed after this period, discontinue use and consult a physician.

Wash hands thoroughly with soap and water immediately after application, unless the hands are the treated area.

Avoid contact with eyes, mucous membranes, and open wounds.

Do not apply an occlusive dressing over the treated area.

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 areas of skin. 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.

Medical Disclaimer

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