Food use
Food-use source coverage is present in the current record.
The ingredient appears in food-oriented source coverage or allowed-use references, which makes food use easier to support than a context with no domain signal at all.
2-Ethylhexyl salicylate / Octisalate) is listed in Annex VI of the EU Cosmetics Regulation (EC) 1223/2009 (UV filters allowed in cosmetic products).
Concern score
The concern value reflects this ingredient's chemical identity — its hazard profile from the published classifications and regulatory status below — not the safety of a product it appears in. A score near 40 is the baseline for ingredients with no specific signal (water scores 40 by design), so a mid-range value is not a safety verdict.
Concern score 25/100 (minor) · high confidence.
Prevalence of OCTISALATE in our catalog (epa_cpdat).
Products
4,882
Brands
6
Typical roles
Catalog
Context-specific fit derived from published classifications and the current ingredient evidence profile.
Food use
Food-use source coverage is present in the current record.
The ingredient appears in food-oriented source coverage or allowed-use references, which makes food use easier to support than a context with no domain signal at all.
Fragrance avoidance
Not a strong fit for fragrance avoidance because it carries Fragrance.
Primary documents currently linked to this ingredient record.
Structured claim signals pulled from linked ingredient research.
Published jurisdiction-level classifications and regulatory designations for this ingredient.
EU
EC
Annex VI of EU Cosmetics Regulation (EC) 1223/2009: UV filters allowed in cosmetic products. Maximum concentration: 5%
US
EPA
EPA CPDat observed this chemical in 4882 composition records across product categories including Personal care, Batteries, Construction. EPA CPDat classifies this chemical for functional uses including UV stabilizer, Fragrance.
US
FDA
Kids spray solaire
Cien Sun
The ingredient itself is a fragrance-linked signal, so it is better treated as an avoid case when fragrance exposure is the main concern.
The published evidence profile currently shaping this ingredient record.
Route: TOPICAL; Dosage form: SOLUTION; Maximum daily exposure: 300 mg
US
FDA
Route: TRANSDERMAL; Dosage form: SOLUTION; Potency: 5 %w/v
US
FDA
Route: TRANSDERMAL; Dosage form: SPRAY; Potency: 8.5 %w/v
US
FDA
FDA NDC lists this ingredient in 37 active drug products and 37 total products.
US
FDA
FDA NDC lists this ingredient in 3182 active drug products and 3245 total products.
US
FDA
openFDA substance registry classifies this ingredient as chemical.