Mupirocin
Bactroban nasal ointment (referred to as Bactroban in this leaflet) contains the antibiotic mupirocin in the form of calcium mupirocin.
It is used:
If the patient is allergic to mupirocin or any of the other ingredients of Bactroban (listed in section 6).
In case of doubts related to the use of the medicine, consult a doctor or pharmacist.
Tell your doctor or pharmacist about all medicines you are taking now or have taken recently, including those obtained without a prescription and herbal medicines, as well as any medicines you plan to take.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.
Always use this medicine exactly as your doctor or pharmacist has told you. If you are not sure, consult your doctor or pharmacist.
Bactroban should be applied twice a day into the nose.
Instead of using the little finger to apply the ointment, a cotton swab can be used.
Special precautions should be taken with these patients. Bactroban should not be used in newborns and infants.
Use Bactroban for as long as your doctor has prescribed. If you have any doubts, consult your doctor or pharmacist. The bacteria in the nose usually die after 3-5 days of treatment.
Do not use Bactroban for more than 10 days.
If you use more Bactroban than you should, consult your doctor or pharmacist. Carefully remove any excess ointment.
If you swallow Bactroban, contact your doctor immediately and tell them how much you have swallowed.
If you forget to use your medicine, use it as soon as you remember. If it is almost time for your next dose, skip the missed dose.
Do not use a double dose to make up for a forgotten dose.
If you stop using Bactroban too early, not all the bacteria may be killed or they may multiply again. Ask your doctor or pharmacist when to stop using the ointment.
In case of doubts related to the use of the medicine, consult a doctor or pharmacist.
Like all medicines, Bactroban can cause side effects, although not everybody gets them.
The following side effects may occur:
If you experience any of these symptoms, contact your doctor as soon as possible.
If you experience any side effects, including any side effects not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, phone: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl.
By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children.
Store in a temperature below 25°C.
Do not use this medicine after the expiry date stated on the packaging.
The expiry date refers to the last day of the month stated.
Do not use Bactroban if it looks different from normal (see description in section 6).
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Bactroban is a white ointment with a uniform consistency. The medicine is available in tubes containing 3 g of ointment, in a cardboard box.
GlaxoSmithKline S.A.
266 Kifissias Ave
Halandri, 15 232 Athens, Greece
Glaxo Operations UK LTD
Barnard Castle, United Kingdom
InPharm Sp. z o.o.
ul. Strumykowa 28/11, 03-138 Warsaw
InPharm Sp. z o.o. Services sp. k.
ul. Chełmżyńska 249, 04-458 Warsaw
Authorization number in Greece, the country of export:50770/4-7-2013
41679/10-9-2009
Parallel import authorization number:368/17
Date of leaflet approval: 28.09.2022
[Information about the trademark]
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