SCHOLL ATHLETES FOOT is a brand name for Tolnaftate. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Prevention and treatment of Athlete’s Foot
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Adults:
Recommended Dose: Twice daily, in the morning and at night. Treatment should continue for up to two weeks after the symptoms disappear.
Paediatric population:
Children aged 2 years and over: As above for adults.
Children under 2 years old:
Not recommended for children under 2 years unless advised by a health care professional. Method of administration Topical. For best results the feet should be washed and dried before use. Shake can before use. Point nozzle towards the affected area, holding it 10-15cm away.
Spray liberally over the affected area. Wear clean socks or hosiery. Apply liberally to the affected area.
Adverse reactions which have been associated with Tolnaftate have been ranked under headings of system organ class and frequency.
Frequencies are defined using the following convention:
Very common ≥ 1/10 Common ≥ 1/100 to ≥ 1/10 Uncommon ≥ 1/1,000 to < 1/100 Rare ≥ 1/10,000 to < 1/1,000 Very rare <1/10,000 Not known (cannot be estimated from the available data) Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.
System Organ Class Frequency Adverse Events Skin and Subcutaneous Tissue Disorders Not Known Skin reaction, skin irritation, pruritus, dermatitis contact. Reporting of Suspected Adverse Reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
It allows continued monitoring of the benefit/risk balance of the medicinal product. uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
For external use only Keep out of eyes If symptoms do not improve within 10 days, discontinue use and consult your doctor. Flammable, pressurised container. Protect from direct sunlight and do not expose to temperatures exceeding 50°C.
Do not spray on naked flame or incandescent material. Do not pierce or burn even after use. Contains butylated hydroxytoluene (E321). g. contact dermatitis), or irritation to the eyes and mucous membranes. 8% w/w alcohol (ethanol). It may cause burning sensation on damaged skin.
If irritation or rash occurs, use of the product should be discontinued and medical advice should be sought.
Contraindicated in nail or scalp infections. 1.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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