Inforin Activ (Gel) Instructions for Use
Marketing Authorization Holder
Spey Medical, Ltd (United Kingdom)
Manufactured By
Balkanpharma-Razgrad, AD (Bulgaria)
ATC Code
M02AA (Topical non-steroidal anti-inflammatory drugs)
Active Substances
Ibuprofen (Rec.INN registered by WHO)
Levomenthol (Rec.INN registered by WHO)
Dosage Form
| Inforin Activ | Gel for external use 50 mg+30 mg/1 g: 40 g tube |
Dosage Form, Packaging, and Composition
Gel for external use homogeneous, transparent, from colorless to light yellow.
| 1 g | |
| Ibuprofen | 50 mg |
| Levomenthol | 30 mg |
Excipients: purified water – up to 1 g, ethanol 96% – 400 mg, propylene glycol – 50 mg, diisopropanolamine – 57 mg, carbomer interpolymer, type A – 20 mg.
40 g – lacquered aluminum tubes (1) – cardboard packs.
Clinical-Pharmacological Group
NSAIDs for external use
Pharmacotherapeutic Group
Nonsteroidal anti-inflammatory drug (NSAID)
Pharmacological Action
Ibuprofen non-selectively blocks the enzymes COX-1 and COX-2, thereby suppressing the synthesis of prostaglandins – mediators of pain, inflammation, and the 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.
Cmax in plasma with topical application is 5% of the Cmax level with oral administration.
Ibuprofen is metabolized 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 externally only. Use on intact skin.
Apply a thin layer of gel to the affected area. Use an amount of gel corresponding to the size of the painful area; a strip of 4 to 10 cm is typically sufficient.
Gently massage the gel into the skin until fully absorbed.
Apply up to four times within 24 hours. Maintain intervals of at least 4 hours between applications.
The maximum duration of continuous use is 10 days.
Wash hands thoroughly with soap and water after each application, unless the hands are the treated area.
If symptoms persist after 10 days of use, or if they worsen, discontinue use and consult a physician.
Do not use an occlusive dressing over the application site.
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 application 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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