Mupirocin 2% nasal ointment
Requires a prescription from a doctor or prescriber
Mupirocin, formerly termed pseudomonic acid A,[A178531] is a novel antibacterial agent with a unique chemical structure and mode of action apart from other antibiotic agents.
Safety information for pregnancy and breastfeeding
Pregnancy
Always consult your doctor or midwife before taking any medicine during pregnancy or while breastfeeding. Source: DrugBank (CC BY-NC 4.0).
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Mupirocin
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Submit a Yellow Card report to the MHRA
Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Mupirocin
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Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
11 branded products available
MHRA licensed products
View all licensed products for Mupirocin on the MHRA register
Bactroban 2% nasal ointment
Bactroban 2% nasal ointment
Mupirocin 2% nasal ointment
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(4)
Impetigo: antimicrobial prescribing (NG153)
Surgical site infections: prevention and treatment (NG125)
Secondary bacterial infection of eczema and other common skin conditions: antimicrobial prescribing (NG190)
Leg ulcer infection: antimicrobial prescribing (NG152)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
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Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 24 · Randomised trials: 11 · 1996–2026
Showing the 50 most relevant studies, sorted by most relevant.
M. Dadashi, Bahareh Hajikhani, D. Darban-Sarokhalil, et al.
Journal of global antimicrobial resistance, 2020
S. George, A. Leasure, D. Horstmanshof
Dimensions of Critical Care Nursing, 2016
M. Phillips, A. Rosenberg, B. Shopsin, et al.
Infection control and hospital epidemiology, 2014
R. Nair, E. Perencevich, A. Blevins, et al.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2016
A. Shittu, M. Kaba, Shima M. Abdulgader, et al.
Antimicrobial Resistance and Infection Control, 2018
Zhou X, Valido E, Krebs J, et al.
2026
- Staphylococcus aureus
- Staphylococcal Infections
- Surgical Wound Infection
ObjectivesTo determine whether mupirocin-based decolonization, compared with placebo, no treatment, or alternative agents, reduces Staphylococcus aureus-related surgical site infection (SA-SSI), nasal S. aureus colonization, and overall SSIs incidence in elective surgery.MethodsWe searched EMBASE, Medline (Ovid), PubMed, CENTRAL, and Google Scholar to May 15, 2024, for randomized controlled trials (RCTs). Risk ratios (RRs) were pooled using a random-effects model with the restricted maximum likelihood estimator with the Hartung-Knapp adjustment. Prespecified subgroup analyses evaluated application strategy, surgical type, and chlorhexidine gluconate (CHG) co-administration.ResultsSeventeen RCTs (15,533 participants) were included. In trials with no-treatment or placebo controls, mupirocin-based decolonization reduced SA-SSI (RR 0.67, 95% confidence interval (CI) 0.49-0.91) and nasal colonization (RR 0.22, 95% CI 0.18-0.26). Effects were larger with targeted use in confirmed carriers and when combined with CHG. No reduction was observed for overall SSIs, except in orthopedic surgery (RR 0.80, 95% CI 0.65-0.99). Head-to-head data vs active alternatives were sparse and did not show a consistent advantage for mupirocin.ConclusionTargeted preoperative mupirocin, especially when combined with CHG, reduces SA-SSI in elective surgery. The lack of significant impact on overall SSIs is interpreted as a reflection of polymicrobial etiologies in surgical infections. Given the emerging risk of mupirocin resistance, further adequately powered head-to-head trials with standardized outcomes and integrated resistance surveillance are warranted.
Abstract licence: CC BY-NC-ND
Allen G
2025
Chia-Chi Tsai, Po-Sheng Yang, Chien-Liang Liu, et al.
American journal of surgery, 2018
Y. Obata, M. Murashima, Naohiro Toda, et al.
Renal Replacement Therapy, 2020
Li Wang, Qianhui Ji, Xiaoyang Hu
Experimental and Therapeutic Medicine, 2021
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
20 to 40 minutes
Mechanism
Mupirocin specifically and reversibly binds to bacterial isoleucyl transfer-RNA…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
[L10580]…
Half-life
20 to 40 minutes
Protein binding
95%
[L10580]
Volume of distribution
Metabolism
[L10580]…
Elimination
2%
Clearance
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L10580]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 53 interactions
The oral LD50 value in rats is 5000 mg/kg.MSDS Studies evaluating the carcinogenic potential of mupirocin have not been performed. In various in vivo animal and in vitro bacterial assays, there was no evidence of genotoxicity caused by mupirocin. In reproduction studies using male and female rats, there were no signs of impaired fertility upon subcutaneous administration of mupirocin.
[L10580]
Use in special populations
Mupirocin was found to be excreted in human milk.
As there is limited data on the use of topical mupirocin in pregnant women, the use of this drug in these patients should be undertaken with caution. Based on the findings in clinical trials, topical mupirocin was shown to be safe and effective in pediatric patients aged 2 months to 16 years.
[L10580]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L10580]
Occlusive dressings do not significantly enhance drug absorption, but damaged skin may allow enhanced penetration of the drug across the skin barrier.
[A178552]
[L6349]
[L10580]
[L10580]
[L10580]
ATC R01AX06
ATC D06AX09
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Mupirocin
Additional database identifiers
Drugs Product Database (DPD)
1832
ChemSpider
393914
BindingDB
50290686
PDB
MRC
ZINC
ZINC000004102194
GenBank Gene Database
X74219
GenBank Protein Database
437916
UniProt Accession
SYI1_STAAU
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q413578), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.