Scholl Corn Removal 40% W/W Medicated Plasters
Out of date information, search anotherSUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Scholl Com Removal 40% w/w Medicated Plasters Scholl Corn Removal 40% w/w Medicated Gel Pads Scholl Corn Removal 40% w/w Medicated Pads
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Salicylic acid 40.00%w/w
For full excipients, see section 6.1
3. PHARMACEUTICAL FORM
Medicated plaster.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
For the treatment of corns Topical application to the skin
4.2 Posology and method of administration
Adults and Children aged 16 years and over
For the best results the feet should be washed and dried before use. One medicated disc should be placed on the corn, covered with a cover plaster or pad. This should be repeated daily until the corn can be removed. Treatment should not continue for more than two weeks, except under medical advice.
Should not be used in children under 16 years, except following a doctor’s recommendation.
4.3 Contraindications
• Not to be used by diabetics or patients with severe circulatory disorders or suffering from neuropathy, , except following a doctor’s prescription and recommendation.
• Not to be used if the corn or surrounding skin is broken or inflamed.
• Not to be used on patients who are hypersensitive to salicylic acid or (to other NSAIDs) or to any excipients in section 6.1
• Not to be used by pregnant or breast feeding patients (see section 4.6)
• Not suitable for application to face, ano-genital region, or large areas of the body.
4.4 Special warnings and precautions for use
Discontinue use and remove plaster if excessive discomfort or irritation is experienced or if sensitivity develops.
Do not apply to normal skin.
For external use only
4.5. Interactions with other medicinal products and other forms of interaction
None stated.
4.6 Fertility, pregnancy and lactation
Pregnancy:
There is no data on the use of topical salicylic acid in pregnant women. Therefore the use of this product during pregnancy is contraindicated.
Breast feeding:
Salicylates should be given with caution to breast-feeding mothers because of the possible risk of Reye's syndrome in nursing infants and there is no data on the use of topical salicylic acid in breast feeding women. Therefore the use of this product during breast feeding is contraindicated.
Fertility:
There is no information on the effects of topical salicylic acid and fertility.
4.7. Effects on ability to drive and use machines
None stated.
4.8 Undesirable effects
Local irritation or dermatitis may occur if applied to normal healthy skin surrounding the corn. This may be controlled by temporarily discontinuing use and by carefully applying only to the corn when the treatment is resumed.
4.9 Overdose
Salicylic acid is readily absorbed through the skin, and symptoms of acute systemic salicylate poisoning have been reported after excessive use. Symptoms include dizziness, tinnitus, deafness, sweating, nausea and vomiting, headache, and confusion, and may be controlled by reducing the dosage.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Salicylic acid: Keratolytic agent
Pharmacotherapuetic classification (ATC code): D11 AF
Pharmacodynamic Effects
Salicylates have analgesic, anti-inflammatory and antipyretic properties much of which is ascribed to an inhibition of prostaglandin synthesis. However, the relevant pharmacodynamic effect of salicylic acid for this product is its “keratolytic” action. The mechanism of this effect has been investigated in animals and in man, and appears to be due to a lipid modifying effect in the lipid bilayers of the skin rather than a keratolytic action. It is thought that the salicylic acid increases lipid structure fluidity so allowing moisture to penetrate into areas surrounding the corn. This in turn leads to a pressure build up causing the corn to be pushed upwards. It has been suggested that the occlusive nature of the plaster enhances this effect.
5.2 Pharmacokinetic properties
Salicylic acid can be absorbed following topical application.
5.3 Preclinical safety data
None stated.
6. PHARMACEUTICAL PARTICULARS
6.1. List of excipients
Polyvinyl alkyl ether (low molecular weight)
Polyvinyl alkyl ether (high molecular weight)
Titanium dioxide Liquid paraffin
Antioxidant: 4,4’ -thio-bis-2-tertbutyl-5-methylphenol Red iron oxide Black iron oxide Backing material.
6.2. Incompatibilities
Not relevant.
6.3. Shelf life
3 years unopened 6 weeks after first opening.
6.4 Special precautions for storage
Do not store above 25°C
6.5 Nature and contents of container
Container: Sachet (polyvinylidene chloride coated polyropylene film).
Plasters:
Sachet contents: 4, 6 or 8 medicated adhesive plasters mounted onto a silicone backed paper. 4, 6 or 8 cover plasters mounted onto a silicone backed paper.
Pads:
Sachet Contents: 4 or 6 medicated adhesive discs mounted onto a silicone backed paper. 4 or 6 twill cloth or silicon “polymer gel” cover pads with pressure sensitive adhesive mounted onto a silicone backed paper.
Outer container: polypropylene flow wrap or cardboard carton.
Not all pack sizes may be marketed.
6.6 Special precautions for disposal
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
7 MARKETING AUTHORISATION HOLDER
Scholl Consumer Products Ltd
103-105 Bath Road
Slough
SL1 3UH
UK
PL 00587/5014R.
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DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
17/01/2008
DATE OF REVISION OF THE TEXT
21/01/2013