Fragrance avoidance
No fragrance-linked caution surfaced in the current profile.
This ingredient does not currently read as a fragrance-linked driver in the published evidence and hazard profile.
EPA CPDat observed this chemical in 4364 composition records across product categories including Pet and animal care, Cleaning products and household care, Construction and building 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 · limited confidence.
Prevalence of SODIUM LAURYL SULFATE in our catalog (epa_cpdat).
Products
4,364
Brands
6
Typical roles
Catalog
Co-occurrence
Ingredients that frequently appear alongside SODIUM LAURYL SULFATE in the catalog.
Context-specific fit derived from published classifications and the current ingredient evidence profile.
Fragrance avoidance
No fragrance-linked caution surfaced in the current profile.
This ingredient does not currently read as a fragrance-linked driver in the published evidence and hazard profile.
The published evidence profile currently shaping this ingredient record.
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 4364 composition records across product categories including Pet and animal care, Cleaning products and household care, Construction and building materials. EPA CPDat classifies this chemical for functional uses including Surfactant (surface active agent), Cleaning agent, Emulsifier.
US
FDA
Crema Manos
S'nonas
Route: DENTAL; Dosage form: GEL; Potency: 1.47 %w/w
US
FDA
Route: DENTAL; Dosage form: PASTE, DENTIFRICE; Potency: 1.4 %w/w
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 600 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED PELLETS; Maximum daily exposure: 1 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED, EXTENDED RELEASE; Potency: NA
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 46 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE PELLETS; Maximum daily exposure: 99 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 166 mg
US
FDA
Route: ORAL; Dosage form: GRANULE; Maximum daily exposure: 12 mg
US
FDA
Route: ORAL; Dosage form: PELLET; Maximum daily exposure: 2 mg
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Maximum daily exposure: 64 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION, EXTENDED RELEASE; Potency: 0.08 mg/1ml
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 233 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE; Maximum daily exposure: 6 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE, EXTENDED RELEASE; Maximum daily exposure: 1 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Maximum daily exposure: 123 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 199 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EFFERVESCENT; Potency: 1.5 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 320 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 240 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FOR SUSPENSION; Maximum daily exposure: 264 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Maximum daily exposure: 16 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE; Maximum daily exposure: 3 mg
US
FDA
Route: RESPIRATORY (INHALATION); Dosage form: CAPSULE; Potency: NA
US
FDA
Route: RESPIRATORY (INHALATION); Dosage form: POWDER; Potency: NA
US
FDA
Route: SUBLINGUAL; Dosage form: TABLET; Potency: 1.1 mg
US
FDA
Route: TOPICAL; Dosage form: CREAM; Maximum daily exposure: 214 mg
US
FDA
Route: TOPICAL; Dosage form: LOTION; Maximum daily exposure: 111 mg
US
FDA
Route: TOPICAL; Dosage form: OINTMENT; Maximum daily exposure: 14 mg
US
FDA
Route: TOPICAL; Dosage form: SHAMPOO; Potency: 65 %w/w
US
FDA
Route: TOPICAL; Dosage form: SHAMPOO, SUSPENSION; Potency: 40 %w/v
US
FDA
Route: TOPICAL; Dosage form: SPRAY; Maximum daily exposure: 7 mg
US
FDA
Route: VAGINAL; Dosage form: CREAM; Maximum daily exposure: 12 mg
US
FDA
Route: VAGINAL; Dosage form: INSERT; Maximum daily exposure: 15 mg
US
FDA
FDA NDC lists this ingredient in 6 active drug products and 8 total products.
US
FDA
openFDA substance registry classifies this ingredient as chemical.