Also known as: EINECS 233-267-9, Selenite sodium, UNII-HIW548RQ3W
INCI: SODIUM SELENITE
Sodium Selenite (CAS 10102-18-8) is a cosmetic cosmetic ingredient functioning as Skin conditioning, Antioxidant. Reported NOAEL =0.12 mg/kg bw/day in Rat (ToxValDB_ECHA_IUCLID); EU Regulation 1223/2009 status: restricted, max 1%. Industrial safety data is also available in the chemical safety database. Same-CAS public records also appear in industrial chemical safety and pharmaceutical data.
Auto-generated CPSR Part A draft with source citations
Cross-Vertical Regulatory Divergence
Sodium Selenite is classified GHS Danger (H300, H330, H315, H317, H319, H331, H400, H410) in the chemicals database but is restricted in EU cosmetics at max 1%.
US NotesSelenium sulfide is an OTC active; sodium selenite in cosmetics requires careful justification; not broadly GRAS for topical use
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Safety Data
Margin of Safety, dermal absorption, and sensitization profile summaries for Sodium Selenite.
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Toxicological Studies
10 study endpoints found for Sodium Selenite. 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
=0.12 mg/kg bw/day
oral
Rat
subchronic
ToxValDB_ECHA_IUCLID
NOAEL
=0.14 mg/kg bw/day
oral
Rat
subchronic
ToxValDB_ECHA_IUCLID
NOAEL
=0.2 mg/kg bw/day
oral
Rat
subchronic
ToxValDB_ECHA_IUCLID
NOAEL
=0.35 mg/kg bw/day
oral
Rat
reproduction developmental
ToxValDB_ECHA_IUCLID
NOAEL
=0.36 mg/kg bw/day
oral
Mouse
short-term
ToxValDB_ECHA_IUCLID
NOAEL
=0.4 mg/kg bw/day
oral
Rat
subchronic
ToxValDB_ECHA_IUCLID
NOAEL
=0.68 mg/kg bw/day
oral
Mouse
developmental
ToxValDB_ECHA_IUCLID
NOAEL
=0.756 mg/kg bw/day
oral
Mouse
chronic
ToxValDB_ECHA_IUCLID
NOAEL
=0.9 mg/kg bw/day
oral
Mouse
subchronic
ToxValDB_ECHA_IUCLID
NOAEL
=2 mg/kg bw/day
injection
Rat
developmental
ToxValDB_ECHA_IUCLID
GHS Hazard Classification
Globally Harmonized System classification per ECHA C&L inventory and ILO/WHO International Chemical Safety Cards.
Short-term Exposure Effects
The substance is irritating to the eyes, skin and respiratory tract. The substance may cause effects on the liver, heart, nervous system and gastrointestinal tract. Medical observation is indicated.
Long-term Exposure Effects
Repeated or prolonged contact with skin may cause dermatitis. The substance may have effects on the central nervous system, bone and blood. See Notes.
Routes of Exposure
The substance can be absorbed into the body by inhalation of its aerosol and by ingestion.
EU CLP Annex VI Harmonized Classification
Legally binding harmonized classification per Regulation (EC) No 1272/2008 (CLP) Annex VI.
Sodium Selenite has a safety rating of "MODERATE" in our database. EU status: restricted. US status: permitted. 10 toxicological study endpoint(s) are available in our database.
Is Sodium Selenite allowed in the EU?
Sodium Selenite EU regulatory status: restricted. Maximum allowed concentration: 1%. This is based on EU Regulation 1223/2009 and its amendments.
What does Sodium Selenite do in cosmetics?
Sodium Selenite functions as: Skin conditioning, Antioxidant. It is classified as a cosmetic ingredient in our database. CAS number: 10102-18-8.
What is the NOAEL for Sodium Selenite?
The NOAEL (No Observed Adverse Effect Level) for Sodium Selenite is =0.12 mg/kg bw/day based on a subchronic study via oral route in Rat. A total of 10 study endpoints are available. Source: ToxValDB_ECHA_IUCLID.
Is Sodium Selenite used outside cosmetics?
Sodium Selenite also appears in industrial chemical safety and pharmaceutical data. The cross-vertical cards on this page render same-CAS public rows from the matched databases.
Does Sodium Selenite have different safety status in cosmetics vs industrial chemicals?
Sodium Selenite is classified GHS Danger (H300, H330, H315, H317, H319, H331, H400, H410) in the chemicals database but is restricted in EU cosmetics at max 1%.
Compliance Tools
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