1. Name Of The Medicinal Product
Dual Action Athlete's Foot Spray
2. Qualitative And Quantitative Composition
Active Ingredient | % quantity |
Tolnaftate | 0.12 w/w |
3. Pharmaceutical Form
Dry Powder Spray
4. Clinical Particulars
4.1 Therapeutic Indications
The product is indicated for the adjunctive treatment and prevention of athlete's foot (tinea pedis). It may also be helpful in conditions where tenderness and sweating cause skin irritation. It is also effective in other conditions, such as dhobie itch (tinea cruris) and prickly heat (miliaria).
4.2 Posology And Method Of Administration
Adults, elderly and children over 2 Years
The affected area should be treated morning and night.
Treatment should continue for at least a week after the infection has cleared up.
Children under 2 Years
Not recommended except under the advice and supervision of a doctor
For topical application to the skin.
4.3 Contraindications
Hypersensitivity to any of the ingredients.
4.4 Special Warnings And Precautions For Use
If irritation or hypersensitivity occurs or if the condition does not improve within 10 days or becomes worse, treatment should be discontinued and medical advice sought.
Avoid contact with eyes.
4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction
No clinically significant drug interactions known.
4.6 Pregnancy And Lactation
Safety in pregnancy has not been established. However, no teratogenic effects have been observed in clinical use. In studies in rats and mice, tolnaftate did not exert a deleterious effect on foetal or postnatal development.
If is not known whether topical tolnaftate is secreted into breast milk. However no undesirable effects in breast fed infants whose mothers were using tolnaftate have been reported.
4.7 Effects On Ability To Drive And Use Machines
No adverse effects known.
4.8 Undesirable Effects
Skin reactions occur rarely and may include irritation and contact dermatitis.
4.9 Overdose
Not applicable.
5. Pharmacological Properties
5.1 Pharmacodynamic Properties
Tolnaftate is an established antifungal agent which appears to produce its effects through inhibition of sterol synthesis.
5.2 Pharmacokinetic Properties
No data available.
5.3 Preclinical Safety Data
There are no preclinical data of relevance to the prescriber which are additional to that already included.
6. Pharmaceutical Particulars
6.1 List Of Excipients
Talc extra 5/0 - M20 DEC
Denatured ethanol B grade
Disteardimonium hectorite
Dimethyl ether
6.2 Incompatibilities
Not applicable.
6.3 Shelf Life
24 months.
6.4 Special Precautions For Storage
Store below 25°C.
Caution: Flammable.
Pressurised container, protect from sunlight and do not expose to temperatures exceeding 50°C.
Do not pierce or burn, even after use.
Do not spray on a naked flame or any incandescent material.
Avoid inhalation.
Do not use near, or place container on, polished or painted surfaces. CFC-Free - does not contain CFC's which damage ozone.
6.5 Nature And Contents Of Container
Internally lacquered aluminium can fitted with a continuous spray valve and an actuator.
Pack size: 150 millilitres
6.6 Special Precautions For Disposal And Other Handling
None.
7. Marketing Authorisation Holder
The Boots Company PLC
1 Thane Road West
Nottingham NG2 3AA
8. Marketing Authorisation Number(S)
PL 00014/0520
9. Date Of First Authorisation/Renewal Of The Authorisation
26 April 1996.
10. Date Of Revision Of The Text
June 2001.
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