Is Phenoxyethanol safe in cosmetics?
Phenoxyethanol has a safety rating of "GOOD" in our database. EU status: restricted. US status: permitted. 10 toxicological study endpoint(s) are available in our database.
Also known as: Ethylene glycol monophenyl ether, Phenoxetol, Phenyl cellosolve, 4-06-00-00571, AI3-00752()C (+14 more)
INCI: PHENOXYETHANOL
Phenoxyethanol (CAS 122-99-6) is a cosmetic preservative functioning as Preservative. NOAEL 357 mg/kg bw/day (PDF-verified against ToxValDB ECHA IUCLID); EU Regulation 1223/2009 status: restricted, max 1.0%. Industrial safety data is also available in the chemical safety database. Same-CAS public records also appear in industrial chemical safety, pharmaceutical, and food safety data.
Phenoxyethanol is classified GHS Danger (H302, H318, H319, H335, H336, H320, H361) in the chemicals database but is restricted in EU cosmetics at max 1.0%.
Source: Cosmetics: ingredients.eu status/eu max; Chemicals: ghs classifications.signal word/hazard statement code
For full compliance data across multiple jurisdictions, use the Substance Compliance tool.
Margin of Safety, dermal absorption, and sensitization profile summaries for Phenoxyethanol.
Calculate MoS for your specific formulation with the MoS Calculator.
10 study endpoints found for Phenoxyethanol. NOAEL (No Observed Adverse Effect Level) values are used to calculate the Margin of Safety per SCCS methodology.
| Endpoint | Value | Route | Species | Study Type | Source |
|---|---|---|---|---|---|
| NOAEL | =2 mg/kg | intravenous | - | NOAEL study | SCCS Opinion |
| NOAEL | =2 mg/kg | intravenous | - | NOAEL study | SCCS Opinion |
| NOAEL | =2 mg/kg | intravenous | - | NOAEL study | SCCS Opinion |
| NOAEL | =2 mg/kg | intravenous | - | NOAEL study | SCCS Opinion |
| NOAEL | =2.69 mg/kg/d | dermal | rat | NOAEL study | SCCS Opinion |
| NOAEL | =2.69 mg/kg bw/day | dermal | rabbit | NOAEL study | SCCS Opinion |
| NOAEL | =2.69 mg/kg/d | dermal | rat | NOAEL study | SCCS Opinion |
| NOAEL | =2.69 mg/kg bw/day | dermal | rabbit | NOAEL study | SCCS Opinion |
| NOAEL | =2.69 mg/kg/d | dermal | rat | NOAEL study | SCCS Opinion |
| NOAEL | =2.69 mg/kg bw/day | dermal | rabbit | NOAEL study | SCCS Opinion |
Globally Harmonized System classification per ECHA C&L inventory and ILO/WHO International Chemical Safety Cards.
Pre-calculated NOAEL → SED → MoS audit trail for Phenoxyethanol across SCCS product categories, with measured dermal absorption where available.
NOAEL/LOAEL values cited in official SCCS opinions for Phenoxyethanol.
| NOAEL | LOAEL | Route | Species | Study | DA% (SCCS) | Opinion |
|---|---|---|---|---|---|---|
| 357 mg/kg/day | - | Dermal | Rabbit | Subchronic (repeated dose) (28 days (5 d/week; adjusted from 5/7)) | 80 | SCCS/1575/16 (2016) |
Contact sensitization data for Phenoxyethanol based on clinical patch test studies and IFRA standards.
Source: ESSCA; IVDK; NACDG
Skin absorption and penetration characteristics of Phenoxyethanol, relevant to systemic exposure and MoS calculations.
Source: SCCS Opinion
10 toxicity values from EPA ToxValDB (aggregated from CCTE, HPV, ToxRefDB, IRIS, and other regulatory dossiers).
| Endpoint | Value | Species | Route | Duration | Source |
|---|---|---|---|---|---|
| NOAEL | =80 mg/kg-day | Rat | oral | subchronic | HESS |
| LOAEL | =1000 mg/kg-day | Rabbit | dermal | short-term | ECHA |
| LOAEL | ~1875 mg/kg-day | Mouse | oral | - | ECHA |
| LOAEL | >3700 mg/kg-day | Mouse | oral | - | ECHA |
| LOAEL | ~1875 mg/kg-day | Mouse | oral | - | ECHA |
| NOAEL | ~375 mg/kg-day | Mouse | oral | - | ECHA |
| NOAEL | ~375 mg/kg-day | Mouse | oral | - | ECHA |
| LD50 | =933 mg/kg | Mouse | oral | - | ChemIDplus |
| LD50 | =5510 mg/kg | Rabbit | dermal | - | ChemIDplus |
| LD50 | =1260 mg/kg | Rat | oral | - | ChemIDplus |
Legally binding harmonized classification per Regulation (EC) No 1272/2008 (CLP) Annex VI.
Inserted via ATP: ATP17
Adverse Outcome Pathway data across 5 assays (DPRA, KeratinoSens, hCLAT, LLNA, NESIL) aggregated from public sources.
Source: DPRA: Hoffmann et al., 2018; KS: No reference provided in NICEATM database; hCLAT: No reference provided in NICEATM database; HPPT: [321] RIFM (1982): RIFM report number 1643, January 13, unpublished.
4 human repeat insult patch tests aggregated from dermatological literature.
| Test Type | N | Sensitized | Dose µg/cm² | NESIL µg/cm² | Potency |
|---|---|---|---|---|---|
| HMT | - | 0 | 6750 | - | - |
| HMT | - | 0 | 6750 | - | - |
| HRIPT | - | 0 | 8266.68 | - | - |
| HRIPT | - | 0 | 12000 | - | - |
Cross-referenced EDC classifications, mechanism data, and dose-response evidence from EDLists, SIN List, and cosmetic-specific detail sources.
Source list: II
weak agonist
| Endpoint | Target | Value | Direction |
|---|---|---|---|
| NOAEL_development | developmental | 486 mg/kg/day | - |
| NOAEL_reproduction | reproductive | 400 mg/kg/day | - |
| dermal_absorption_rinseoff | skin | 37% % | - |
| dermal_absorption_leaveon | skin | 78–81% % | - |
| ERα agonistic activity screening | ERα | EC50/IC50: No significant ER agonism at non-cytotoxic concentrations in most assays; some studies show LOEC ~100 µM; LOEC: ~100 µM (reported in some studies); NOEC: not established mixed | weak agonist (borderline active) |
| FT4 / FT3 levels (epidemiological association); thyroid gene expression (zebrafish) | Thyroid axis (TR / HPT) | EC50/IC50: In vitro EC50 not established; LOEC ~1 mg/L (zebrafish thyroid gene expression); LOEC: ~1 mg/L (zebrafish); NOEC: not established mixed | thyroid disruptor (suggestive) |
European Chemicals Agency REACH dossier and Substances of Very High Concern listing.
European Commission CosIng database Annex references per Regulation (EC) No 1223/2009.
Additional regulatory detail beyond the 7-jurisdiction summary: Saudi SFDA, Korea MFDS, ASEAN ACD, Japan/Korea, Brazil/India, and cross-jurisdictional restriction entries.
| Jurisdiction | Status | Max % | Product Type |
|---|---|---|---|
| JP | restricted | 1.0% | All cosmetics |
| CN | permitted_preservative | 1 | All cosmetics |
| IN | permitted_preservative | 1.0 | all cosmetics |
| AU | restricted | 1.0 | preservatives |
| GCC | restricted | 1.0 | All cosmetics |
| BR | permitted_preservative | 1 | - |
| ASEAN | permitted_preservative | 1.0% | All products |
Cross-database dermal penetration: EPA Dryad physics-based, Roberts Mendeley permeation, and SCCS-aggregated measured values.
| Type | DA % | Method | Skin Model | SCCS Ref |
|---|---|---|---|---|
| measured_sccs_opinion | 80.0% | - | - | SCCS/1633/21 |
| measured_sccs_opinion | 47.0% | - | - | SCCS/1575/16 |
| measured_sccs_opinion | 47.0% | - | - | SCCS/1575/16 |
Reported concentration ranges per product category from SCCS/CIR/industry sources.
| Product Category | Typical Range | Max Reported | Source |
|---|---|---|---|
| Face Cream | 0.5–1 | 1 | CIR Safety Assessment |
| Body Lotion | 0.5–1 | 1 | CIR Safety Assessment |
| Shampoo | 0.5–1 | 1 | CIR Safety Assessment |
| Serum | 0.5–1 | 1 | CIR Safety Assessment |
| Conditioner | 0.5–1 | 1 | CIR Safety Assessment |
Safety and regulatory annotations from PubChem (NCBI) aggregated sources.
Preliminary editorial summary for Phenoxyethanol — not a computed safety verdict. See the sourced toxicological data above.
Public NOAEL study rows linked to Phenoxyethanol by CAS number or substance name.
Units vary across source rows: mg/kg, mg/kg/d, mg/kg bw/day
| Absorption % | Method | Vehicle |
|---|---|---|
| 80.0% | SCCS opinion extraction | - |
| 47.0% | SCCS PDF direct extraction | - |
| 47.0% | SCCS PDF direct extraction | - |
Same-CAS public records found in pharmaceutical and food safety data.
Same-CAS rows from the pharmaceutical spoke database.
Same-CAS food additive or FDA GRAS records from the core public database.
Phenoxyethanol has a safety rating of "GOOD" in our database. EU status: restricted. US status: permitted. 10 toxicological study endpoint(s) are available in our database.
Phenoxyethanol EU regulatory status: restricted. Maximum allowed concentration: 1.0%. This is based on EU Regulation 1223/2009 and its amendments.
Phenoxyethanol functions as: Preservative. It is classified as a Preservative in our database. CAS number: 122-99-6.
The NOAEL (No Observed Adverse Effect Level) for Phenoxyethanol is =2 mg/kg based on a NOAEL study study via intravenous route in rat. A total of 10 study endpoints are available. Source: SCCS Opinion.
Phenoxyethanol also appears in industrial chemical safety, pharmaceutical, and food safety data. The cross-vertical cards on this page render same-CAS public rows from the matched databases.
Phenoxyethanol is classified GHS Danger (H302, H318, H319, H335, H336, H320, H361) in the chemicals database but is restricted in EU cosmetics at max 1.0%.
Check Phenoxyethanol compliance across multiple jurisdictions:
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