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.
EPA CPDat observed this chemical in 1566 composition records across product categories including Food and drug, Pesticides, Raw materials.
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 5/100 (low) · high confidence.
Prevalence of POLYSORBATE 80 in our catalog (epa_cpdat).
Products
1,566
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.
US
EPA
EPA CPDat observed this chemical in 1566 composition records across product categories including Food and drug, Pesticides, Raw materials. EPA CPDat classifies this chemical for functional uses including Emulsifier, Fragrance, Surfactant (surface active agent).
US
FDA
Route: AURICULAR (OTIC); Dosage form: DROPS; Potency: 0.02 %w/w
US
FDA
Effaclar duo+
La Roche-Posay
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: AURICULAR (OTIC); Dosage form: SOLUTION; Potency: 0.2 %w/w
US
FDA
Route: AURICULAR (OTIC); Dosage form: SOLUTION/ DROPS; Maximum daily exposure: 13 mg
US
FDA
Route: AURICULAR (OTIC); Dosage form: SUSPENSION; Potency: 1 %w/v
US
FDA
Route: INTRA-ARTICULAR; Dosage form: INJECTION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRA-ARTICULAR; Dosage form: INJECTION, POWDER, FOR SUSPENSION; Maximum daily exposure: 5 mg
US
FDA
Route: INTRA-ARTICULAR; Dosage form: INJECTION, SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRALESIONAL; Dosage form: INJECTION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRALESIONAL; Dosage form: INJECTION, SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION; Potency: 4 %w/v
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, POWDER, FOR SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Maximum daily exposure: 1 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, SOLUTION; Potency: 5 %w/v
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRASYNOVIAL; Dosage form: INJECTION; Potency: 0.2 %w/v
US
FDA
Route: INTRASYNOVIAL; Dosage form: INJECTION, SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: INTRAVENOUS; Dosage form: CONCENTRATE; Maximum daily exposure: 4680 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION; Maximum daily exposure: 4680 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: 53 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Maximum daily exposure: 900 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Maximum daily exposure: 1170 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION, CONCENTRATE; Maximum daily exposure: 4739 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SUSPENSION; Potency: 0.5 %w/v
US
FDA
Route: INTRAVENOUS; Dosage form: LIQUID; Maximum daily exposure: 720 mg
US
FDA
Route: INTRAVENOUS; Dosage form: SOLUTION; Maximum daily exposure: 900 mg
US
FDA
Route: INTRAVITREAL; Dosage form: INJECTION, SUSPENSION; Potency: 0.02 %w/v
US
FDA
Route: NASAL; Dosage form: SPRAY, METERED; Potency: 0.1 mg/1ml
US
FDA
Route: OPHTHALMIC; Dosage form: DROPS; Potency: 0.05 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: EMULSION; Maximum daily exposure: 26 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Maximum daily exposure: 8 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION, GEL FORMING, EXTENDED RELEASE; Potency: 0.05 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Potency: 0.25 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION; Maximum daily exposure: 1 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION/ DROPS; Maximum daily exposure: 1 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED; Potency: 0.04 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED PELLETS; Potency: 2 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 23 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 10 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, LIQUID FILLED; Maximum daily exposure: 24 mg
US
FDA
Route: ORAL; Dosage form: CONCENTRATE; Potency: 1 mg/1ml
US
FDA
Route: ORAL; Dosage form: ELIXIR; Potency: 2.5 mg/15ml
US
FDA
Route: ORAL; Dosage form: GRANULE, FOR SUSPENSION; Maximum daily exposure: 240 mg
US
FDA
Route: ORAL; Dosage form: PASTE; Maximum daily exposure: 28 mg
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Maximum daily exposure: 150 mg
US
FDA
Route: ORAL; Dosage form: SOLUTION; Maximum daily exposure: 907 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION; Maximum daily exposure: 206 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION, EXTENDED RELEASE; Maximum daily exposure: 40 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION/ DROPS; Maximum daily exposure: 23 mg
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 233 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE; Maximum daily exposure: 84 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Maximum daily exposure: 18 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 4 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 10 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Potency: 24 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED, EXTENDED RELEASE; Potency: 8 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Maximum daily exposure: 1 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE; Maximum daily exposure: 34 mg
US
FDA
Route: RECTAL; Dosage form: SOLUTION; Maximum daily exposure: 315 mg
US
FDA
Route: RECTAL; Dosage form: SUPPOSITORY; Potency: 72.15 mg
US
FDA
Route: RESPIRATORY (INHALATION); Dosage form: SUSPENSION; Maximum daily exposure: 1 mg
US
FDA
Route: SOFT TISSUE; Dosage form: INJECTION; Maximum daily exposure: 4 mg
US
FDA
Route: SOFT TISSUE; Dosage form: INJECTION, SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: SUBCUTANEOUS; Dosage form: INJECTION, SUSPENSION; Potency: 0.3 %w/v
US
FDA
Route: SUBCUTANEOUS; Dosage form: SUSPENSION; Potency: 0.3 %w/v
US
FDA
Route: SUBLINGUAL; Dosage form: TABLET; Potency: 0.08 mg
US
FDA
Route: TOPICAL; Dosage form: AEROSOL, FOAM; Potency: 0.98 %w/w
US
FDA
Route: TOPICAL; Dosage form: CREAM; Maximum daily exposure: 20 mg
US
FDA
Route: TOPICAL; Dosage form: EMULSION; Potency: 2.5 %w/w
US
FDA
Route: TOPICAL; Dosage form: GEL; Maximum daily exposure: 12 mg
US
FDA
Route: TOPICAL; Dosage form: OINTMENT; Potency: 0.1 %w/w
US
FDA
Route: TOPICAL; Dosage form: SYSTEM; Maximum daily exposure: 28 mg
US
FDA
Route: VAGINAL; Dosage form: AEROSOL, FOAM; Potency: 3 %w/w
US
FDA
Route: VAGINAL; Dosage form: SUPPOSITORY; Potency: 28 mg
US
FDA
FDA NDC lists this ingredient in 14 active drug products and 14 total products.
US
FDA
openFDA substance registry classifies this ingredient as polymer.