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METAZ 0.1% OINTMENT 30G
- Sku : I-003818
Key features
METAZ 0.1% OINTMENT is a topical ointment containing mometasone furoate 0.1% as the active ingredient. It is a potent topical corticosteroid that binds intracellular glucocorticoid receptors to alter gene transcription, inducing lipocortins and inhibiting phospholipase A2, thereby reducing prostaglandin and leukotriene production to produce anti-inflammatory, antipruritic and vasoconstrictive effects. It is indicated for relief of the inflammatory and pruritic manifestations of corticosteroid‑responsive dermatoses such as atopic dermatitis and psoriasis. Available by prescription as a topical ointment in a 30 g pack.- Brand: METAZ
- Active Ingredient: MOMETASONE FUROATE
- Strength: 0.1%
- Dosage Form: Ointment
- Pack Size: 15 g
- Route: Topical
- Prescription Status: Prescription
- Therapeutic Class: Dermatological
- Pharmacological Group: Corticosteroids (Plain)
- Drug Class: Topical Corticosteroid - Potent (Group III/Class 3), Synthetic glucocorticoid, Dermatological corticosteroid (plain)
- Manufacturer: SPIMACO
- Country of Origin: Saudi Arabia
- SFDA Registration No.: 16-809-17
- Shelf Life: 36 months
- Storage: store below 25°c
- Skin Condition: Eczema, Psoriasis
- Steroid Potency: Potent
Frequently bought together
Indications
Approved Uses
Relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses (e.g., atopic dermatitis and psoriasis).
Off-Label Uses
Off-label uses may include alopecia areata, vitiligo (adjunct), lichen planus (cutaneous), and prurigo nodularis; phimosis is more commonly supported with other topical steroids and is not a typical mometasone-specific off-label use.
Dosage & Administration
Dosing by Condition
For corticosteroid-responsive dermatoses (including eczema/atopic dermatitis and psoriasis): apply a thin layer to affected areas once daily; occlusion is generally avoided and, if considered for resistant psoriasis, should only be under clinician supervision.
Initial Dose
Apply a thin film to the affected skin areas once daily.
Maintenance Dose
Apply a thin film to the affected skin areas once daily. Therapy should be discontinued when control is achieved.
Maximum Dose
Apply a thin film once daily; no universally fixed gram/week maximum is established for mometasone ointment-limit to the smallest amount needed and avoid large surface areas, prolonged continuous use, or occlusion unless directed.
Children's Dosage
For children 2 years of age and older, apply a thin film to the affected area once daily. Use for longer than 3 weeks has not been established. Not recommended for use in children under 2 years of age.
Dose Adjustment Notes
Use the lowest effective amount for the shortest duration; reassess if no improvement within ~2 weeks; once controlled, step down by reducing frequency (e.g., alternate days/2-3 times weekly) and avoid prolonged continuous use, especially on face/intertriginous areas or large surface areas and under occlusion.
How to Take
For topical use only: apply a thin layer to affected skin once daily and rub in gently; wash hands before and after (unless treating hands); avoid eyes, mouth, and other mucous membranes; do not use on face/groin/axillae or under occlusion/bandages unless directed by a clinician.
Side Effects
Common Side Effects
Application-site burning/stinging, pruritus, irritation/dryness/erythema; folliculitis/acneiform eruption; with prolonged use: skin atrophy, striae, telangiectasia, hypopigmentation, and contact dermatitis; secondary infection may occur.
Side Effect Frequency
Common: application-site burning/stinging, pruritus, irritation/dryness. Less common/uncommon: folliculitis, acneiform eruptions, perioral dermatitis, hypopigmentation, hypertrichosis, allergic contact dermatitis, secondary infection, skin atrophy, striae, telangiectasia, miliaria. Rare/with prolonged use, large areas, or occlusion: HPA-axis suppression/Cushingoid effects, hyperglycemia; ocular effects (blurred vision, glaucoma, cataract) have been reported particularly with periocular use.
Safety & Warnings
Contraindications
Contraindicated in hypersensitivity to mometasone furoate or excipients; avoid use on untreated bacterial/viral (e.g., herpes simplex/varicella)/fungal/parasitic skin infections; avoid use in rosacea, perioral dermatitis, and acne vulgaris.
Warnings & Precautions
Avoid eyes/mucosa; do not use under occlusion unless directed; avoid/limit use on face, groin, axillae and do not use for diaper dermatitis; do not apply to infected lesions without appropriate antimicrobial therapy; use the lowest effective amount/shortest duration and consider tapering after long-term use; pediatric patients are at higher risk of systemic toxicity; monitor for skin atrophy and visual symptoms.
Age Restriction
Not recommended for children <2 years; in ≥2 years use the lowest effective amount for the shortest duration.
Driving Warning
Safe
Drug Interactions
Drug Interactions
Clinically relevant interactions are uncommon, but systemic exposure may increase with strong CYP3A inhibitors (e.g., ritonavir/cobicistat/itraconazole/ketoconazole) if absorption is significant; occlusive dressings and concurrent potent topical steroids increase systemic absorption risk.
Interaction Severity
MODERATE: strong CYP3A4 inhibitors (e.g., ritonavir/cobicistat, ketoconazole, itraconazole) may increase systemic corticosteroid effects if significant percutaneous absorption occurs (large areas, prolonged use, occlusion).
Food Interaction
No restriction
Alcohol Interaction
Safe
Special Populations
Pregnancy
Category C
Breastfeeding
Caution
Children
For children 2 years of age and older, apply a thin film to the affected area once daily. Use for longer than 3 weeks has not been established. Not recommended for use in children under 2 years of age.
Elderly
Standard adult dosing; use with caution as elderly skin is more susceptible to atrophy and systemic absorption
Kidney Impairment
No adjustment needed
Liver Impairment
No dose adjustment recommended; use caution with extensive/prolonged use in severe hepatic impairment because systemic corticosteroid exposure could be higher if absorbed.
Storage & Patient Advice
Storage Conditions
Store below 25°C (per SFDA verified API data); keep the tube tightly closed and do not freeze.
Missed Dose
Apply when remembered; if it is close to the next scheduled application, skip the missed dose and resume the regular schedule-do not apply extra to make up for it.
Stopping the Medicine
Stop when control is achieved; if used long-term, on large areas, or under occlusion, taper (reduce frequency/potency) rather than abrupt cessation to reduce rebound/withdrawal and adrenal suppression risk.
Overdose
Excessive/prolonged topical use (especially large areas/occlusion) can cause local adverse effects and systemic corticosteroid toxicity including HPA-axis suppression/Cushingoid features; management is to stop or taper and provide supportive care; if ingested, contact poison control/seek medical care.
Patient Counseling
For topical use only for the prescribed condition. Apply a thin film to affected skin once daily (or as directed) and rub in gently; use the smallest amount for the shortest duration. Avoid eyes, mouth, and mucous membranes; wash hands after use unless treating hands. Do not use on the face, groin, or axillae, on broken/infected skin, or under occlusion (tight bandages/diapers) unless specifically directed. Stop and seek medical advice if irritation, worsening, or signs of infection occur, or if no improvement within ~2 weeks (or as advised). Keep out of reach of children.
Monitoring Requirements
Monitor clinical response and local adverse effects (atrophy, striae, telangiectasia, irritation, secondary infection); in higher-risk use (large surface area, prolonged therapy, occlusion, pediatric patients), periodically evaluate for HPA-axis suppression.
Pharmacology
Mechanism of Action
Topical glucocorticoid: binds intracellular glucocorticoid receptors to alter gene transcription, inducing lipocortins that inhibit phospholipase A2 and downstream prostaglandin/leukotriene production, producing anti-inflammatory, antipruritic, and vasoconstrictive effects.
Onset of Action
Within a few days
Duration of Effect
Up to 24 hours
Half-Life
Not well characterized after topical administration; a definitive systemic half-life is generally not provided for topical mometasone furoate due to minimal absorption.
Bioavailability
Systemic absorption after topical application is low; in studies of 0.1% ointment, about ~0.7% of the applied dose may be absorbed through intact skin, and absorption increases with inflammation, barrier disruption, large surface area, prolonged use, or occlusion.
Metabolism
Any absorbed mometasone furoate is extensively metabolized in the liver to multiple inactive metabolites (CYP3A4 involvement is plausible but not consistently specified as the definitive pathway in standard product information).
Excretion
For the small absorbed fraction, metabolites are eliminated mainly via bile/feces with a minor renal component; timing such as 'within 72 hours' is not a standard, reliably stated parameter for this product.
Protein Binding
Not reliably established/commonly reported for topical mometasone furoate in standard product information; do not state a precise % binding for this product.
Product Information
Available Dosage Forms
Ointment, cream, lotion (and some markets also have topical solution for scalp).
Composition per Dose
Each gram of ointment: 1 mg mometasone furoate (0.1% w/w) in a white petrolatum base
Generic Availability
Yes
OTC Alternatives
No OTC equivalent to mometasone 0.1% potency; for mild disease, OTC hydrocortisone 0.5-1% cream/ointment can be used short-term if appropriate.
Skin Condition
Eczema, Psoriasis
Steroid Potency
Potent
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