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 2153 composition records across product categories including Furniture and furnishings, Construction and building materials, Other indirect contact consumer goods.
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 SULFATE ANHYDROUS in our catalog (epa_cpdat).
Products
2,153
Brands
6
Typical roles
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 2153 composition records across product categories including Furniture and furnishings, Construction and building materials, Other indirect contact consumer goods. EPA CPDat classifies this chemical for functional uses including Viscosity modifier, Absorbent, Filler.
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Potency: 1.14 %w/v
US
FDA
Crème mains hydratante concentrée Formule Norvégienne
Neutrogena
Route: OPHTHALMIC; Dosage form: SOLUTION; Maximum daily exposure: 7 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Potency: 0.17 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION; Potency: 1.2 %w/v
US
FDA
Route: RESPIRATORY (INHALATION); Dosage form: SOLUTION; Potency: 0.03 %w/w
US
FDA
FDA NDC lists this ingredient in 20 active drug products and 20 total products.
US
FDA
openFDA substance registry classifies this ingredient as chemical.