PACKAGE INSERT/PATIENT INFORMATION LEAFLET

PLEASE READ THIS LEAFLET CAREFULLY BEFORE USING

CANESTEN ATOMISER SPRAY

A clear spray containing 1.0% clotrimazole BP.

Canesten atomiser spray also contains isopropanol (30%), propylene glycol and polyethylene glycol 400. The spray is produced by an atomiser and contains no propellant.

The atomiser spray comes in a bottle containing 40ml.

Canesten atomiser spray is one of a group of medicines called imidazoles which are used to treat fungal skin infections.

Product Licence/Authorisation holder:

Bayer plc

Bayer House

Strawberry Hill

Newbury, Berkshire

RG14 1JA

Manufacturer:

Bayer AG, Leverkusen, Germany

 

When should I use Canesten atomiser spray?

Canesten atomiser spray should be used to treat fungal skin infections such as ringworm, athlete's foot and fungal infection of the breast fold (intertrigo). The atomiser spray is particularly suitable for infections covering large and/or hairy areas.

If you are unsure of the cause of your infection, seek the advice of your doctor or pharmacist (chemist).

 

When should I not use Canesten atomiser spray?

Do not use Canesten atomiser spray if you have previously had an allergic reaction to the active ingredient clotrimazole or to propylene glycol. If you are unsure about this, ask your doctor or pharmacist.

 

What special precautions should I take?

Do not allow the Canesten spray to come into contact with eyes, ears, nose or mouth. If this happens accidentally, rinse immediately with water and seek medical advice.

Do not inhale the spray.

Do not use the spray near a naked flame.

If you are pregnant or are planning a family, tell your doctor or pharmacist before using Canesten spray. If you have informed your doctor or pharmacist already, follow their instructions carefully.

 

How do I use Canesten atomiser spray?

If Canesten atomiser spray has been prescribed for you by your doctor, follow any instructions he/she may have given you.

If you have purchased this product without a prescription, follow these directions closely:

 

If symptoms persist, consult your doctor.

Your doctor or pharmacist may recommend that you use an anti-fungal dusting powder as well, particularly for treating athlete's foot.

00056664/5202/UK/1 /974/M-C

You can help the treatment to work if you follow these simple self-help tips:

Your Canesten atomiser spray is for external use only. Avoid contact with eyes, ears, nose and mouth. If contact happens accidentally, rinse immediately with water and seek medical advice.

 

What should I do if I forget to use my Canesten atomiser spray?

Apply the spray as soon as possible and then continue the rest of your treatment as usual.

 

What undesirable effects may I experience?

The symptoms of your skin infection, such as itching or soreness, should improve within a few days of treatment although signs such as redness and scaling may take longer to disappear.

Canesten atomiser spray may cause unwanted effects in some people. You may experience a mild burning or irritation immediately after applying the spray. If you find this intolerable, stop treatment and tell your doctor.

If, upon first use of Canesten atomiser spray, you experience a rash and itching, tell your doctor immediately as you may be allergic to Canesten.

If your symptoms get worse or persist, or you feel you are reacting badly to this medicine in any other way, consult your doctor.

 

How should I store my Canesten atomiser spray?

No special precautions are required but it is best to keep the Canesten atomiser spray in the original carton in a cool, dry place.

KEEP OUT OF THE REACH OF CHILDREN

Do not use the spray after the expiry date which is printed at one end of the carton and on the label of the bottle.

If you find that you still have this medicine after its expiry date, return it to your local pharmacist who will dispose of it properly

REMEMBER: This medicine is for your use only. Do not give it to anyone else under any circumstances. /f you have any doubts about using Canesten atomiser spray correctly, seek the advice of your doctor or pharmacist.

Date of preparation: January 1994

Product Licence Number: 0010/0060 R

Product Authorisation Number: 21/4/5

Distributed in the Republic of Ireland by:

Bayer Ltd.

Dun Laoghaire

Co. Dublin