Phenoxyethanol 2% solution
Requires a prescription from a doctor or prescriber
Phenoxyethanol is a colorless liquid with a pleasant odor.
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MHRA alerts for Phenoxyethanol
Safety monitoring data
Yellow Card reports
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Suspected adverse reactions reported for Phenoxyethanol
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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
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
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Codes for healthcare professionals and prescribing systems
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NHS UK identifiers
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0.
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 · Randomised trials: 2 · 1989–2026
Showing the 50 most relevant studies, sorted by most relevant.
Brigitte Dreno, Torsten Zuberbier, C. Gelmetti, et al.
Journal of the European Academy of Dermatology and Venereology, 2019
Beales E, Clements MN, Feasey NA, et al.
2026
- Anti-Infective Agents, Local
- Infectious Disease Transmission, Vertical
- Neonatal Sepsis
ImportanceNeonatal sepsis causes substantial mortality. Topical antisepsis for laboring women or neonates may reduce pathogenic colonization and sepsis risk.ObjectiveTo evaluate the safety and effectiveness of various topical antiseptic regimens to reduce bacterial load in the maternal genital tract and on neonatal skin and assess suitability for future effectiveness trials.Design, setting, and participantsThis randomized clinical trial was conducted from March 7, 2022, to March 29, 2023, at Zomba Central Hospital, Malawi, with 28-day follow-up. Participant populations were laboring women and, separately, facility-born neonates (aged 1000 g) not born to a mother recruited to the trial. Data were analyzed from May 17 to December 28, 2023.InterventionsParticipants were individually randomized in an unblinded factorial design to chlorhexidine 1% (1% CHG), chlorhexidine 2% (2% CHG), or octenidine 0.1% with phenoxyethanol 2% (OHP), each applied either once or multiple times (maternal: antiseptic applied every 4 hours during working hours for up to 6 applications; neonatal: antiseptic applied every 24 hours for up to 3 applications), or to standard of care (SOC; application of sterile water for mothers and no cleansing for neonates). Laboratory staff assessing primary outcomes were blinded.Main outcomes and measuresCo-primary outcomes were change in total skin bacterial load (log10 colony-forming units [log10CFU]) from baseline at each follow-up, analyzed separately in the maternal and neonatal populations and adjusted for intervention variables. Secondary outcomes included skin condition score (range, 0-12 for neonates and 0-16 for women; lower scores indicate better condition), serious adverse events (SAEs), and neonatal temperature.ResultsA total of 149 women (mean [SD] age at enrollment, 25.7 [5.9] years) and 147 neonates (mean [SD] age at enrollment, 10.3 [6.3] hours; 82 [56%] male) participated. Mean (SD) infant gestational age was 37.7 (1.5) weeks in the maternal population and 36.7 (3.1) weeks in the neonatal population. Neonates' mean birth weight was 2729 g (712 g). Among mothers, compared with 1% CHG, bacterial load was higher (worse) with OHP (adjusted log10CFU difference, 1.7; 95% CI, 0.9-2.5) and SOC (3.5; 95% CI, 2.4-4.6); there was no clear log10CFU difference with 2% CHG (-0.6; 95% CI, -1.4 to 0.2). There was no evidence of difference in effectiveness between multiple vs single application (log10CFU difference, -0.4; 95% CI, -1.1 to 0.2). In neonates, 1% CHG showed greater effectiveness than SOC (log10CFU difference, 1.3; 95% CI, 0.2-2.4) but no difference vs 2% CHG (-0.2; 95% CI, -1.1 to 0.7) or OHP (0.7; 95% CI, -0.2 to 1.6). Multiple applications showed increasing benefits over time (frequency × time interaction). Skin scores were low (almost all were 0-1 and none ≥3). There were no significant differences in SAE rates between arms and no signal of postantiseptic neonatal hypothermia.Conclusions and relevanceIn this randomized clinical trial of topical antiseptics applied in laboring women and in neonates, 1% CHG reduced maternal and neonatal bacterial colonization without safety concerns, suggesting it would be the optimal regimen to evaluate in a larger pragmatic trial powered for clinical outcomes.Trial registrationISRCTN Registry Identifier: ISRCTN78026255.
Abstract licence: CC BY
O. Idoko, Robert B Mboizi, Michael E Okoye, et al.
Vaccine, 2017
Yayue Zheng, Yuxin Yu, Wenqian Lin, et al.
Bioresource technology, 2021
Wuhuan Li, Xuesong Tan, Changlin Miao, et al.
Green Chemistry, 2023
Yayue Zheng, Xiaoxue Zhao, Wenqian Lin, et al.
Industrial Crops and Products, 2023
Amit Agrawal, Umesh Pandwar, Nitin Pandya
Indian Journal of Child Health, 2022
Phenoxyethanol is used at concentrations below 1% as a preservative in cosmetic products and fixative in perfumes. Some people have reported adverse responses to phenoxyethanol on their skin. Some suggest that the test subjects' negative reactions are the result of allergies. Nevertheless, there are claims that it's simply a skin irritant that has varying degrees of effect on various people. In 2012, the ANSM (French National Agency of Medicine and Health Products Safety) advised against using Phenoxyethanol in cosmetics for babies' bottoms. On a European level, this advice had not been confirmed. The purpose of this article is to discuss the potential negative effects of phenoxyethanol on newborns and infants.
Abstract licence: CC BY-NC-ND 4.0
N.S. Mattson, T.H. Riple
Aquaculture, 1989
Brynley Crosado, S. Löffler, B. Ondruschka, et al.
Anatomical Sciences Education, 2019
J. Scognamiglio, L. Jones, C.S. Letizia, et al.
Food and Chemical Toxicology, 2012
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
1 found
Half-life
Not available
Mechanism
Phenoxyethanol has antibacterial properties and is effective against strains of…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Volume of distribution
75.4%
Metabolism
60-70%
[L2618]
…
Elimination
90%
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Phenoxyethanol (EU), or PE, is the most commonly used globally-approved preservative in personal care formulations. It is very easy to use in various types of formulations and is chemically stable. Phenoxyethanol is a colorless, clear, oily liquid with a faint aromatic odor at room temperature and a low water solubility and evaporation rate. It is produced by reacting phenol (EU) and ethylene oxide (EU) at a high temperature and pressure. This substance occurs naturally in green tea (EU) [L2621].
According to the European Union Cosmetics Regulation (EC) n.1223/2009, phenoxyethanol is authorized as a preservative in cosmetic formulations at a maximum concentration of 1.0% [L2625].
Phenoxyethanol has been classified as an antimicrobial and preservative by Health Canada [L2623]. It has also been used in vaccines and shown to inactivate bacteria, and several types of yeast [A32838].
[L2618], [L2619], [L2625]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 16 of 16 interactions
LD50 Rabbit dermal 2250 mg/kg .
[L2618]
2-Phenoxyethanol (PhE) has been shown to induce hepatotoxicity, renal toxicity, and hemolysis at dosages ≥ 400 mg/kg/day in subchronic and chronic studies in multiple species .
[A32847]
The major hazards encountered in the use and handling of 2-phenoxyethanol stem from its toxicologic properties. Toxic by all routes (inhalation, ingestion, and dermal contact), exposure to this very faintly aromatic, colorless, oily liquid may occur from its use as a fixative for cosmetics, perfumes, and soaps; as a bactericide and insect repellant; as a solvent for cellulose acetate,dyes, stamp pad, ball point, and specialty inks; as a chemical intermediate for carboxylic acid esters (eg, acrylate, maleate) and polymers (eg, formaldehyde, melamine); and as a preservative for human specimens used for dissection and demonstrations in anatomical studies. Effects resulting from exposure to this substance can include eye irritation, headache, tremors, and central nervous system depression.
If contact with the eyes occurs, irrigate exposed eyes with copious amounts of tepid water for at least 15 minutes, and wash exposed skin thoroughly with soap and water. 2-Phenoxyethanol must be preheated before ignition can occur .
[L2623]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L2629]
The absolute topical bioavailability of PE was 75.4% and 76.0% for emulsion and lotion, respectively. Conversion of PE to PAA was extensive, with the average AUCPAA-to-AUCPE ratio being 4.4 and 5.3 for emulsion and lotion, respectively. The steady-state tissue-to-plasma PE concentration ratio (Kp) was higher than unity for kidney, spleen, heart, brain, and testis and was lower (0.6) for lung and liver, while the metabolite Kp ratio was higher than unity for kidney, liver, lung, and testis and was lower (0.3) for other tissues .
[L2629]
[L2618]
The rate of intestinal absorption was rapid, with 60-70% of the excreted (14)C detected at 3 hours and > 95% of the total 4-day urinary (14)C detected within the first 24 hr. Trace amounts of radioactivity were detected in feces. Four days after dosing, only trace amounts of radioactivity remained in the carcass, primarily in the liver (< 0.2% of the dose), fat and muscle.
At the 4 day point, the (14)C concentration in blood was measured to be only 0.001 .
[L2618]
The major metabolite of phenoxyethanol is phenoxyacetic acid .
[L2629]
About 2% and 1.3% of the ingested dose was recovered from the exhaled air of female and male rats, respectively .
[L2618]
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)
Phenoxyethanol
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