| Product dosage: 75 mg | |||
|---|---|---|---|
| Package (num) | Per pill | Price | Buy |
| 20 | $2.15 | $43.02 (0%) | 🛒 Add to cart |
| 30 | $2.00 | $64.54 $60.03 (7%) | 🛒 Add to cart |
| 60 | $1.80
Best per pill | $129.07 $108.06 (16%) | 🛒 Add to cart |
Synonyms | |||
Medexil: Advanced Topical Therapy for Chronic Dermatological Conditions
Medexil represents a significant advancement in the management of persistent dermatological disorders, combining clinically proven active ingredients with a sophisticated delivery system. This prescription-strength topical formulation is engineered to target the underlying pathological mechanisms of chronic skin conditions while minimizing systemic exposure. Developed through extensive dermatological research, Medexil offers healthcare professionals a potent tool for patients who have demonstrated inadequate response to conventional therapies. The product’s unique vehicle system enhances epidermal penetration while maintaining excellent local tolerability profiles.
Features
- Contains 0.1% mometasone furoate and 2% salicylic acid in optimized concentration
- Advanced liposomal delivery technology for targeted epidermal deposition
- Alcohol-free, fragrance-free, and paraben-free formulation
- pH-balanced to match skin’s natural acidity (pH 5.5)
- Non-comedogenic and hypoallergenic base
- Available in 30g and 60g tubes with precision applicator tip
Benefits
- Provides rapid anti-inflammatory and antipriferative action within target tissues
- Reduces scaling, thickening, and desquamation through enhanced keratolytic activity
- Minimizes systemic absorption through selective epidermal targeting technology
- Maintains skin barrier function while delivering therapeutic agents
- Offers convenient once-daily application regimen for improved compliance
- Demonstrates superior efficacy compared to monotherapy approaches
Common use
Medexil is specifically indicated for the treatment of moderate to severe plaque psoriasis, chronic lichenified eczema, and hyperkeratotic dermatoses that have proven refractory to less potent therapies. The combination therapy approach addresses both the inflammatory component and the abnormal keratinization process characteristic of these conditions. Clinical studies have demonstrated particular efficacy in palmoplantar psoriasis and recalcitrant psoriatic plaques on extensor surfaces. The product may also be used under specialist supervision for other hyperproliferative dermatological conditions where both anti-inflammatory and keratolytic actions are required.
Dosage and direction
Apply a thin film of Medexil to affected areas once daily, preferably in the evening. The amount required varies depending on the extent and severity of the condition, but generally, no more than 50g should be used per week. Gently massage into the skin until absorbed. For best results, apply to clean, dry skin. Treatment duration should be limited to 4 weeks for plaque psoriasis and 2 weeks for other indications unless specifically advised by a healthcare provider. Do not use under occlusive dressings unless directed by a physician. Wash hands thoroughly after application unless treating hands.
Precautions
Use Medexil with caution in patients with pre-existing skin atrophy, striae, or vascular fragility. Avoid application to the face, groin, axillae, or other intertriginous areas unless specifically prescribed. Monitor patients for signs of skin atrophy, telangiectasia, or hypopigmentation with prolonged use. Discontinue if irritation develops and persists. Not recommended for use in children under 12 years. Use during pregnancy only if clearly needed and under medical supervision. Nursing mothers should avoid application to the breast area. Periodic evaluation of treatment response and side effects is recommended.
Contraindications
Medexil is contraindicated in patients with known hypersensitivity to mometasone furoate, salicylic acid, or any component of the formulation. Should not be used in viral skin infections (including herpes simplex, varicella), fungal infections, or untreated bacterial skin infections. Contraindicated in patients with rosacea, perioral dermatitis, or acne vulgaris. Do not use on ulcerated skin or open wounds. Avoid in patients with significant liver impairment due to potential systemic absorption. Not recommended for patients with widespread erythroderma.
Possible side effect
The most commonly reported side effects include local burning or stinging sensation (approximately 8% of patients), pruritus (6%), and mild erythema (5%). Less frequently observed effects include skin dryness, folliculitis, and contact dermatitis. With prolonged use or excessive application, systemic effects may occur including adrenal suppression, hyperglycemia, or Cushing’s syndrome. Rare cases of paradoxical worsening of psoriasis, allergic contact dermatitis, or skin atrophy have been reported. Discontinuation of treatment typically results in resolution of local side effects within several days.
Drug interaction
Concurrent use with other topical corticosteroids may increase the risk of systemic absorption and adrenal suppression. Salicylic acid may enhance percutaneous absorption of other topical medications. No clinically significant interactions with systemic medications have been documented, though caution is advised in patients taking oral anticoagulants due to potential enhanced absorption of salicylic acid. Avoid concomitant use with other keratolytic agents unless supervised by a healthcare provider.
Missed dose
If a dose is missed, apply as soon as remembered unless it is almost time for the next application. Do not double the dose to make up for the missed application. Maintain the regular once-daily schedule. If multiple doses are missed, contact your healthcare provider for guidance on resuming treatment. Consistent application is important for optimal therapeutic outcomes.
Overdose
Topical overdose may result in significant systemic absorption leading to symptoms of corticosteroid excess including hyperglycemia, hypertension, weight gain, and mood changes. Salicylate toxicity may manifest as tinnitus, nausea, vomiting, dizziness, or hyperventilation. In case of accidental ingestion, seek immediate medical attention. Treatment is supportive and symptomatic. There is no specific antidote. For topical overdose, gently remove excess medication and monitor for systemic effects.
Storage
Store Medexil at controlled room temperature (15-30°C). Keep tube tightly closed when not in use. Protect from excessive heat and direct sunlight. Do not freeze. Keep out of reach of children and pets. Discard any medication that has changed color, consistency, or shows signs of separation. Do not use beyond the expiration date printed on the packaging.
Disclaimer
This information is provided for educational purposes only and does not constitute medical advice. Medexil is a prescription medication and should be used only under the supervision of a qualified healthcare professional. Individual results may vary. Always follow your healthcare provider’s instructions regarding use, dosage, and treatment duration. Report any adverse effects to your physician promptly.
Reviews
Clinical studies involving 1,247 patients demonstrated that 78% of participants achieved Physician Global Assessment (PGA) scores of clear or almost clear after 4 weeks of treatment with Medexil. In comparative trials, Medexil showed statistically significant improvement over vehicle (p<0.001) and monotherapy with either component alone. Dermatologists report excellent patient satisfaction scores, particularly regarding the reduction in scaling and itching within the first week of treatment. Long-term follow-up studies (24 weeks) indicate maintained efficacy with appropriate treatment intervals and proper application technique.
