Summary of Product Characteristics
last updated on the eMC:
27/04/2007
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SPC
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Canesten Dermatological Powder /Canesten AF Dual Action Powder
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Go to top of the page | Canesten Dermatological Powder (also available as Canesten AF Dual Action Powder) | |
Go to top of the page | Clotrimazole 1% w/w. For excipients, see 6.1. | |
Go to top of the page | Powder for topical application. | |
Go to top of the pageGo to top of the page | Legal Category P Canesten Dermatological Powder should be used externally as an adjunct to treatment with Canesten Cream, Solution or Dermatological Spray and as a prophylactic against reinfection, particularly in infections involving skin folds, and where perspiration is a problem.Legal Category GSL Should be used as an adjunct to treatment with Canesten AF Dual Action Cream or Canesten AF Dual Action Spray and as a prophylactic against reinfection of tinea pedis (athlete's foot) only. | |
Go to top of the page | Canesten Dermatological Powder should be sprinkled onto the affected areas two to three times daily after using Canesten Cream, Solution or Dermatological Spray. The powder may also be dusted inside articles of clothing and footwear which are in contact with the infected area. | |
Go to top of the page | Hypersensitivity to clotrimazole or the excipient rice starch. Legal Category GSL Only Do not use the powder to treat nail or scalp infections. | |
Go to top of the pageGo to top of the pageGo to top of the page | Data on a large number of exposed pregnancies indicate no adverse effects of Clotrimazole on pregnancy or on the health of the foetus/newborn child. To date, no relevant epidemiological data are available. Clotrimazole can be used during pregnancy, but only under the supervision of a physician or midwife. | |
Go to top of the pageGo to top of the page | Rarely patients may experience local mild burning or irritation immediately after applying the powder. Very rarely the patient may find this irritation intolerable and stop treatment.Other undesirable effects:Body as a whole: | allergic reaction, pain | Skin and appendages: | pruritis, rash |
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Go to top of the page | In the event of accidental oral ingestion, routine measures such as gastric lavage should be performed only if clinical symptoms of overdose become apparent (e.g. dizziness, nausea or vomiting). It should be carried out only if the airway can be protected adequately. | |
Go to top of the pageGo to top of the page | ATC Code: D01A C01 Clotrimazole is an imidazole derivative with a broad spectrum of antimycotic activity. It also exhibits activity against Trichomonas, staphylococci, streptococci and Bacteroides. It has no effect on lactobacilli. Mechanism of Action Clotrimazole acts against fungi by inhibiting ergosterol synthesis. Inhibition of ergosterol synthesis leads to structural and functional impairment of the cytoplasmic membrane. Pharmacodynamic Effects Clotrimazole has a broad antimycotic spectrum of action in vitro and in vivo, which includes dermatophytes, yeasts, moulds, etc. The mode of action of clotrimazole is fungistatic or fungicidal depending on the concentration of clotrimazole at the site of infection. In-vitro activity is limited to proliferating fungal elements; fungal spores are only slightly sensitive. Primarily resistant variants of sensitive fungal species are very rare; the development of secondary resistance by sensitive fungi has so far only been observed in very isolated cases under therapeutic conditions. | |
Go to top of the page | Pharmacokinetic investigations after dermal application have shown that clotrimazole is practically not absorbed from the intact or inflamed skin into the human blood circulation. The resulting peak serum concentrations of clotrimazole were below the detection limit of 0.001 μg/ml, reflecting that clotrimazole applied topically does not lead to measurable systemic effects or side effects. | |
Go to top of the page | There are no preclinical data of relevance to the prescriber which are additional to those already included in other sections of the Summary of Product Characteristics. | |
Go to top of the pageGo to top of the pageGo to top of the pageGo to top of the pageGo to top of the page | No special storage requirements. | |
Go to top of the page | Polyethylene powder canister with a perforated conical plug for dusting and a screw cap. The canister contains 30g of powder. | |
Go to top of the pageGo to top of the page | Bayer plc Bayer House Strawberry Hill Newbury, Berkshire RG14 1JA. Trading as Bayer plc, Consumer Care Division | |
Go to top of the pageGo to top of the page | Date of first authorisation: | 27 July 1978 | Date of last renewal: | 8 January 1999 |
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Go to top of the pageGo to top of the page | Canesten Dermatological Powder | P | Canesten AF Dual Action Powder | GSL |
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