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MICONAZ CREAM 20G
- Sku : I-003831
Key features
MICONAZ CREAM 20G is a vaginal cream containing miconazole nitrate 2% as the active ingredient. As an imidazole antifungal, it works by inhibiting fungal cell membrane synthesis and disrupting the growth of Candida organisms. It is indicated for the treatment of vulvovaginal candidiasis (vaginal yeast infection). Available OTC as a vaginal cream in a 40 g pack.- Brand: MICONAZ
- Active Ingredient: MICONAZOLE NITRATE 2%
- Strength: 2%
- Dosage Form: Vaginal cream
- Pack Size: 40 g
- Route: Vaginal use
- Prescription Status: OTC
- Therapeutic Class: Dermatological
- Pharmacological Group: Antifungals (Topical)
- Drug Class: Imidazole Antifungal (Topical)
- Manufacturer: DEEF PHARMACEUTICAL INDUSTRIES
- Country of Origin: Saudi Arabia
- SFDA Registration No.: 2708245834
- Shelf Life: 24 months
- Storage: store below 30°c
- Skin Condition: Fungal
Indications
Approved Uses
Vulvovaginal candidiasis (vaginal yeast infection).
Off-Label Uses
Not applicable/insufficiently supported for this specific SFDA-registered vaginal cream; do not recommend off-label dermatologic uses with a vaginal formulation.
Dosage & Administration
Dosing by Condition
Vulvovaginal candidiasis: intravaginal miconazole 2% cream, typically 5 g (one applicatorful) once daily at bedtime for 7 days (per common guideline/OTC regimens).
Initial Dose
For vaginal use (2% cream): 1 applicatorful intravaginally every night at bedtime for 7 days; not typically used as topical application with specified gram amounts
Maintenance Dose
For vaginal 2% cream: 1 applicatorful every night for 7 days (not a maintenance dose regimen); treatment is typically a single 7-day course, not continued for 2-4 weeks
Maximum Dose
Not applicable as a systemic maximum; use only as per labeled vaginal regimen (e.g., typical intravaginal course) and do not exceed recommended frequency/duration without medical advice.
Children's Dosage
Children under 12 years: safety and efficacy not established; not recommended for vaginal use in prepubertal children. Children 12 years and older: same as adult dosing (1 applicatorful every night for 7 days)
How to Take
This SFDA-registered product is a vaginal cream (miconazole nitrate 2%): wash hands; preferably apply at bedtime using the supplied applicator to insert the prescribed amount intravaginally (commonly one applicatorful) for the full course; avoid intercourse/tampons during treatment if advised; wash hands after use and clean applicator if reusable.
Side Effects
Common Side Effects
Local irritation such as burning, stinging, itching, redness/erythema; less commonly rash/contact dermatitis (and for vaginal use, pelvic/vaginal discomfort may occur).
Side Effect Frequency
Common: local burning/irritation/itching/erythema; Uncommon: rash/contact dermatitis; Rare: hypersensitivity reactions (e.g., angioedema/anaphylaxis)
Safety & Warnings
Contraindications
Hypersensitivity to miconazole (miconazole nitrate) or to any excipient in the formulation.
Warnings & Precautions
For vaginal use only (not oral/ophthalmic); avoid eye contact; stop if significant irritation/sensitization occurs; may weaken latex condoms/diaphragms during treatment; if on warfarin/coumarins monitor for bleeding/INR changes; seek medical advice if first episode, recurrent/persistent symptoms, or possible non-yeast causes.
Age Restriction
Vaginal miconazole 2%: generally intended for post‑pubertal/adult use; do not use in children <12 years unless directed by a clinician.
Driving Warning
Safe
Drug Interactions
Drug Interactions
Latex condoms/diaphragms may be weakened (functional interaction).
Food Interaction
No restriction
Special Populations
Pregnancy
Consult Doctor
Children
Children under 12 years: safety and efficacy not established; not recommended for vaginal use in prepubertal children. Children 12 years and older: same as adult dosing (1 applicatorful every night for 7 days)
Elderly
Standard adult dosing.
Storage & Patient Advice
Stopping the Medicine
Complete the full recommended course even if symptoms improve; stop and seek medical advice if severe irritation/allergic reaction occurs or if symptoms persist/return.
Overdose
Topical/vaginal overdose is unlikely; if accidentally ingested, contact poison control/seek medical care-manage supportively (possible GI upset such as nausea/vomiting).
Patient Counseling
Vaginal use: use at bedtime with applicator and complete the full course; wash hands before/after; avoid eyes/oral use; the cream may weaken latex condoms/diaphragms during and shortly after use-use alternative contraception; seek care if severe irritation/allergy, fever/pelvic pain, foul-smelling discharge, or no improvement after completing therapy; if on warfarin, inform clinician and monitor for bleeding; store below 30°C.
Monitoring Requirements
No routine monitoring required for topical use. Monitor INR in patients on warfarin
Pharmacology
Onset of Action
Symptom improvement for vulvovaginal candidiasis often begins within 1-3 days, but complete cure requires finishing the full 7-day course.
Duration of Effect
Local antifungal effect persists with regular dosing during the treatment course; clinical cure requires completing the full regimen and symptoms may recur if therapy is stopped early.
Product Information
Available Dosage Forms
For this product: vaginal cream. (Miconazole as an ingredient is also available in other markets as topical dermatologic cream/powder/spray and vaginal suppositories/pessaries; availability varies by country/registration.)
Composition per Dose
Each 1 gram of cream contains 20mg of Miconazole Nitrate (2%)
Generic Availability
Yes
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.
Al Mujtama Pharmacy assumes no legal or medical liability for:
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- Any discrepancy between the information provided and the product's package insert or SFDA guidelines
- Any misuse of medication resulting from personal interpretation of the content displayed
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