Hexetidine 0.1% mouthwash sugar free
Available from pharmacies, supermarkets, and retail outlets
A bactericidal and fungicidal antiseptic.
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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 Hexetidine
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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.
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Suspected adverse reactions reported for Hexetidine
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2 branded products available
MHRA licensed products
View all licensed products for Hexetidine on the MHRA register
Oraldene 0.1% mouthwash peppermint
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.
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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
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NHS UK identifiers
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. 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: 3 · 1959–2025
Showing the 50 most relevant studies, sorted by most relevant.
W. R. Roberts, M. Addy
Journal Of Clinical Periodontology, 1981
- Bacteria
- Biguanides
- Cetylpyridinium
F Afennich, DE Slot, N Hossainian, et al.
International Journal of Dental Hygiene, 2010
- Anti-Infective Agents, Local
- Chlorhexidine
- Dental Plaque
Saxer Up, Mühlemann Hr
PubMed, 1983
- Clinical Trials as Topic
- Dental Plaque
- Dental Plaque Index
Banu Uygun-Can, Tanju Kadir
Infection and Drug Resistance, 2025
Purpose: Intraoral concentrations of antimicrobial agents such as hexetidine (HEX) using alternative antimycotics fluctuate significantly due to the dynamics in the oral cavity, which can affect both the virulence capacity and the outcome of antimycotic therapy in the management of denture stomatitis-associated oral candidiasis. Methods: This study was carried out to evaluate the impact of different sub-therapeutic HEX concentrations (1/100, 1/200) for different times (0.5, 2, 24, 48 h) on the expression levels of the virulence ( hwp1, plb1, plb2, sap4, sap5, sap6 ) and drug-resistance ( cdr1, cdr2, mdr1, erg11 ) genes of Candida albicans SC5314. Total RNA was extracted immediately after antimicrobial exposure. The qRT-PCR data were performed using the comparative 2 −ΔΔCT method to calculate the relative expression of the target genes after treatment to HEX concentrations, standardized to the actin housekeeping gene. Results: Expression levels of the hwp1 and plb1 genes decrease after exposure to HEX to higher concentrations at 0.5 h, while the expression level of the plb2 gene increases. Only the expression of the erg11 gene showed a significant decrease within the resistance genes at 0.5 h. Sap5, plb2 , and mdr1 are overexpressed at 48 h. Sub-therapeutic levels of HEX affect the virulence and drug-resistance genes of C. albicans . Conclusion: These results give an idea of future strategies for developing and using HEX as an adjunctive therapy for oral candidiasis. The innovation and clinical relevance of our research lie in its exploration of how low doses of HEX influence gene expression over varying time periods, potentially paving the way for alternative therapeutic strategies. Keywords: antimicrobial agents, hexetidine, virulence genes, drug-resistance genes, oral candidiasis, Candida albicans
Abstract licence: CC BY-NC 3.0
Elvedina Kapić, Fahir Bečić, Ervina Bečić
PubMed, 2002
- Anti-Infective Agents, Local
- Hexetidine
- Mouth
Georges Aoun
PubMed, 2016
C. Bosi, A. Davin-Régli, R. Charrel, et al.
The Journal of hospital infection, 1996
- Anti-Infective Agents, Local
- Disease Outbreaks
- Drug Contamination
David S. Jones, James G. McGovern, A. David Woolfson, et al.
Pharmaceutical Research, 2002
- Bacterial Adhesion
- Intubation, Intratracheal
- Analysis of Variance
Ogun
West African Journal of Medicine, 2022
- Anti-Infective Agents, Local
- COVID-19
- Mouth
A. Bergenholtz, L. Hänström
Community dentistry and oral epidemiology, 1974
- Biguanides
- Dental Plaque
- Dental Prophylaxis
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
Not available
Mechanism
Not available
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medicines. Always consult a healthcare professional.
Showing 14 of 14 interactions
ATC G01AX16
ATC A01AB12
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)
Hexetidine
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72