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 52 composition records across product categories including Laboratory supplies, Food and drug, Landscape/yard.
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 CALCIUM CHLORIDE in our catalog (fda_ndc).
Products
152
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 52 composition records across product categories including Laboratory supplies, Food and drug, Landscape/yard. EPA CPDat classifies this chemical for functional uses including Fragrance, Chemical reaction regulator, Processing aids not otherwise specified.
US
FDA
Route: INFILTRATION; Dosage form: INJECTION; Potency: 0.33 mg
US
FDA
Cool Wave
Gillette
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: INTRA-ARTERIAL; Dosage form: INJECTION, SOLUTION; Maximum daily exposure: 11 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION; Potency: 4 %w/v
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, SOLUTION; Potency: 0.01 %w/v
US
FDA
Route: INTRAOCULAR; Dosage form: SOLUTION; Maximum daily exposure: 24 mg
US
FDA
Route: INTRAPERITONEAL; Dosage form: SOLUTION; Potency: 0.03 %w/v
US
FDA
Route: INTRATHECAL; Dosage form: INJECTION, SOLUTION; Maximum daily exposure: 1 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTABLE, LIPOSOMAL; Potency: 0.03 %w/v
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION; Potency: 4 %w/v
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Maximum daily exposure: 11 mg
US
FDA
Route: INTRAVITREAL; Dosage form: INJECTION, SUSPENSION; Potency: 0.05 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Maximum daily exposure: 1 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Potency: 0.02 %w/v
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 2 mg
US
FDA
Route: ORAL; Dosage form: CONCENTRATE; Potency: 0.08 mg/1ml
US
FDA
Route: RESPIRATORY (INHALATION); Dosage form: CAPSULE; Maximum daily exposure: 3 mg
US
FDA
FDA NDC lists this ingredient in 127 active drug products and 152 total products.
US
FDA
openFDA substance registry classifies this ingredient as chemical.