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LICAN 1% CREAM 30G
- Sku : I-028934
Key features
LICAN 1% Cream is a topical formulation containing luliconazole 10 mg/g (1%) as the active antifungal ingredient. It inhibits fungal lanosterol 14α‑demethylase (CYP51), reducing ergosterol synthesis and disrupting fungal cell membrane integrity and function. Indicated for the treatment of interdigital tinea pedis, tinea cruris, and tinea corporis. Available as a 30 g tube and supplied by prescription only.- Brand: LICAN
- Active Ingredient: LULICONAZOLE 10mg/g
- Strength: 10mg/g
- Dosage Form: Cream
- Pack Size: 30 g
- Route: Topical
- Prescription Status: Prescription
- Therapeutic Class: Dermatological
- Pharmacological Group: Antifungals (Topical)
- Drug Class: Imidazole Antifungal (Topical)
- Manufacturer: Jamjoom Pharmaceuticals Factory Company
- Country of Origin: Saudi Arabia
- SFDA Registration No.: 1612246422
- Shelf Life: 24 months
- Storage: store below 30°c
- Skin Condition: Fungal
Frequently bought together
Indications
Approved Uses
Interdigital tinea pedis, tinea cruris, tinea corporis
Off-Label Uses
None routinely recommended; do not list onychomycosis or pityriasis (tinea) versicolor as standard off-label uses for luliconazole cream.
Dosage & Administration
Dosing by Condition
Tinea pedis: apply once daily for 2 weeks; Tinea cruris: apply once daily for 1 week; Tinea corporis: apply once daily for 1 week.
Initial Dose
Apply a thin layer to the affected area and approximately 1 inch of surrounding skin once daily
Maintenance Dose
Apply once daily for the prescribed duration (1 week for tinea cruris/corporis, 2 weeks for tinea pedis).
Maximum Dose
Apply a thin layer once daily to affected area(s) (no systemic maximum dose is defined for topical use).
Children's Dosage
Safety and efficacy in pediatric patients have not been established.
Dose Adjustment Notes
No dose adjustment is required (including renal/hepatic impairment) because systemic absorption is minimal with topical use.
How to Take
Clean and dry the affected area before application. Apply a thin layer of cream to the affected skin and approximately 1 inch of surrounding area once daily. Rub in gently. Wash hands after application unless hands are the treated area.
Side Effects
Common Side Effects
Application-site reactions (e.g., burning, stinging, itching/pruritus, erythema/redness, irritation; less commonly contact dermatitis)
Side Effect Frequency
Uncommon (<1%): application-site reactions (e.g., irritation/burning/stinging/pruritus/erythema); post-marketing: contact dermatitis, cellulitis (frequency not known)
Safety & Warnings
Contraindications
Hypersensitivity to luliconazole or any component of the formulation.
Warnings & Precautions
For external (topical) use only; avoid eyes, mouth, and other mucous membranes; not for ophthalmic, oral, or intravaginal use; discontinue and seek advice if significant irritation/sensitization or allergic reaction occurs; use only on indicated skin areas (not nails/scalp unless directed).
Age Restriction
Safety and efficacy in pediatric patients have not been established.
Driving Warning
Safe
Drug Interactions
Drug Interactions
Clinically significant drug interactions are unlikely with topical luliconazole due to minimal systemic absorption; no meaningful in-vivo interaction data exist, and any in-vitro CYP inhibition is of uncertain clinical relevance.
Interaction Severity
No clinically significant drug interactions expected/known with topical luliconazole.
Food Interaction
No restriction
Special Populations
Pregnancy
Consult Doctor
Breastfeeding
Consult Doctor
Children
Safety and efficacy in pediatric patients have not been established.
Elderly
Standard adult dosing.
Kidney Impairment
No adjustment needed.
Liver Impairment
No adjustment needed.
Storage & Patient Advice
Stopping the Medicine
Complete the full prescribed course; it is appropriate to stop after the recommended duration is finished even if symptoms improved earlier.
Overdose
Topical overdose is unlikely; if accidental ingestion occurs, seek urgent medical advice/poison center and provide supportive care as needed.
Patient Counseling
Apply once daily to clean, dry skin covering the affected area and a small margin around it; wash hands before/after (unless treating hands); avoid eyes/mouth/mucosa; complete the full prescribed course; do not occlude unless directed; stop and seek care if severe irritation or allergic reaction occurs; store below 30°C.
Monitoring Requirements
No routine laboratory monitoring; monitor clinically for local skin irritation/hypersensitivity and treatment response.
Pharmacology
Mechanism of Action
Inhibits fungal lanosterol 14α-demethylase (CYP51), reducing ergosterol synthesis and disrupting fungal cell membrane integrity/function.
Onset of Action
Symptom improvement may begin within a few days (often 2-3 days); assess clinical response by the end of the prescribed course (typically 1-2 weeks).
Duration of Effect
Clinical antifungal effect is maintained with once-daily application throughout the full treatment course; durable cure is assessed after completing therapy (typically 1-2 weeks), rather than as a single fixed hour-based duration.
Half-Life
Unknown / not established for topical luliconazole
Bioavailability
Low systemic absorption after topical application; absolute bioavailability is not well established/clinically relevant.
Metabolism
Unknown / not well characterized for topical luliconazole (systemic metabolism not clinically relevant at topical doses)
Excretion
Unknown / not well characterized for topical luliconazole due to minimal systemic absorption
Protein Binding
>99%
Product Information
Available Dosage Forms
Cream
Composition per Dose
Each gram of cream contains: 10mg luliconazole.
Skin Condition
Fungal
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The product information provided is derived from verified pharmaceutical references and is intended for general health education only. It is not a substitute for professional medical advice, diagnosis, or treatment.
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