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Intranasal Mupirocin and Topical Chlorhexidine

University of Maryland, Baltimore · FDA-approved active Small molecule

Intranasal Mupirocin and Topical Chlorhexidine is a Topical antibiotic combination Small molecule drug developed by University of Maryland, Baltimore. It is currently FDA-approved for Prevention of surgical site infections by reducing nasal Staphylococcus aureus colonization, Decolonization of methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage.

Intranasal mupirocin and topical chlorhexidine work together to eliminate and prevent nasal colonization of pathogenic bacteria, particularly Staphylococcus aureus.

Intranasal mupirocin and topical chlorhexidine work together to eliminate and prevent nasal colonization of pathogenic bacteria, particularly Staphylococcus aureus. Used for Prevention of surgical site infections by reducing nasal Staphylococcus aureus colonization, Decolonization of methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage.

At a glance

Generic nameIntranasal Mupirocin and Topical Chlorhexidine
SponsorUniversity of Maryland, Baltimore
Drug classTopical antibiotic combination
TargetBacterial isoleucyl-tRNA synthetase (mupirocin); bacterial cell membrane and proteins (chlorhexidine)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Mupirocin is a topical antibiotic that inhibits bacterial protein synthesis by binding to isoleucyl-tRNA synthetase, effectively killing susceptible bacteria in the nasal cavity. Chlorhexidine is a broad-spectrum antimicrobial agent that disrupts bacterial cell membranes and denatures proteins. Together, this combination targets and eradicates nasal carriage of antibiotic-resistant pathogens, reducing the risk of subsequent infection.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Intranasal Mupirocin and Topical Chlorhexidine

What is Intranasal Mupirocin and Topical Chlorhexidine?

Intranasal Mupirocin and Topical Chlorhexidine is a Topical antibiotic combination drug developed by University of Maryland, Baltimore, indicated for Prevention of surgical site infections by reducing nasal Staphylococcus aureus colonization, Decolonization of methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage.

How does Intranasal Mupirocin and Topical Chlorhexidine work?

Intranasal mupirocin and topical chlorhexidine work together to eliminate and prevent nasal colonization of pathogenic bacteria, particularly Staphylococcus aureus.

What is Intranasal Mupirocin and Topical Chlorhexidine used for?

Intranasal Mupirocin and Topical Chlorhexidine is indicated for Prevention of surgical site infections by reducing nasal Staphylococcus aureus colonization, Decolonization of methicillin-resistant Staphylococcus aureus (MRSA) nasal carriage.

Who makes Intranasal Mupirocin and Topical Chlorhexidine?

Intranasal Mupirocin and Topical Chlorhexidine is developed and marketed by University of Maryland, Baltimore (see full University of Maryland, Baltimore pipeline at /company/university-of-maryland-baltimore).

What drug class is Intranasal Mupirocin and Topical Chlorhexidine in?

Intranasal Mupirocin and Topical Chlorhexidine belongs to the Topical antibiotic combination class. See all Topical antibiotic combination drugs at /class/topical-antibiotic-combination.

What development phase is Intranasal Mupirocin and Topical Chlorhexidine in?

Intranasal Mupirocin and Topical Chlorhexidine is FDA-approved (marketed).

What are the side effects of Intranasal Mupirocin and Topical Chlorhexidine?

Common side effects of Intranasal Mupirocin and Topical Chlorhexidine include Nasal irritation or discomfort, Local allergic reaction, Headache.

What does Intranasal Mupirocin and Topical Chlorhexidine target?

Intranasal Mupirocin and Topical Chlorhexidine targets Bacterial isoleucyl-tRNA synthetase (mupirocin); bacterial cell membrane and proteins (chlorhexidine) and is a Topical antibiotic combination.

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