Lidocaine 0.5% / Cetylpyridinium chloride 0.1% oromucosal gel sugar free
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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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1 branded products available
Part of the Dentinox brand family (generic: Lidocaine + Cetylpyridinium)
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View all licensed products for Lidocaine + Cetylpyridinium on the MHRA register
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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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: 27 · Randomised trials: 12 · 1994–2026
Showing the 50 most relevant studies, sorted by most relevant.
Yanxia Sun, Tianzuo Li, Nan-yue Wang, et al.
Diseases of the Colon & Rectum, 2012
S. Weibel, Y. Jelting, N. Pace, et al.
The Cochrane database of systematic reviews, 2018
Lauren K. Dunn, M. Durieux
Anesthesiology, 2017
H. Hermanns, M. Hollmann, M. Stevens, et al.
British journal of anaesthesia, 2019
S. Weibel, J. Jokinen, N. Pace, et al.
British journal of anaesthesia, 2016
J. Lee, C. Sanderson, W. Xuan, et al.
Journal of Palliative Medicine, 2019
M. Bailey, T. Corcoran, S. Schug, et al.
PAIN, 2018
Yuan-Ching Chang, Chien-Liang Liu, Tsang‐Pai Liu, et al.
Pain Practice, 2017
Windhorst ER, Joosstens M, van der Sluijs E, et al.
2025
- Dental Plaque
- Gingivitis
- Chlorhexidine
AimTo evaluate the effectiveness of cetylpyridinium chloride (CPC) and chlorhexidine (CHX) mouthwashes (MW) on plaque and gingivitis scores for patients with gingivitis, in brushing as well as non-brushing situations.MethodsA comprehensive search of MEDLINE-PubMed and Cochrane-CENTRAL was conducted to identify clinical and randomised controlled trials comparing CPC and CHX mouthwashes on plaque and gingivitis scores. The staining index was evaluated as a secondary outcome. In addition, the risk of bias was assessed. The data was summarised using a descriptive approach, and whenever possible, a meta-analysis was conducted. The results for brushing and non-brushing studies were presented separately. Grading was applied using the GRADE approach to rate the certainty of evidence.ResultsThe search resulted in 424 unique papers, from which 14 full-text papers providing 18 comparisons were selected. Different concentrations of CPC-MW (0.1%, 0.075%, 0.05%) and CHX-MW (0.2%, 0.12%) were used. The risk of bias was estimated to be low, moderate or high for each study. A meta-analysis for non-brushing models showed a significant favour for CHX-MW in plaque index scores (0.55 [95% CI: 0.19; 0.91], p = 0.003). For brushing, no significant differences were found between CPC-MW and CHX-MW. The descriptive analysis supports these findings. CHX-MW tends to stain more than CPC-MW.ConclusionThere is moderate certainty for a small statistically significant favourable effect of CHX-MW over CPC-MW for plaque control in non-brushing situations, but no difference between them for plaque and gingivitis prevention in brushing situations.
Abstract licence: CC BY
Xiaojun Mao, D. Auer, W. Buchalla, et al.
Antimicrobial Agents and Chemotherapy, 2020
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.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.