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 2802 composition records across product categories including Construction and building materials, Furniture and furnishings, Cleaning and safety.
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 SODIUM CARBONATE in our catalog (epa_cpdat).
Products
2,802
Brands
6
Typical roles
Catalog
Co-occurrence
Ingredients that frequently appear alongside SODIUM CARBONATE in the 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
No fragrance-linked caution surfaced in the current profile.
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 2802 composition records across product categories including Construction and building materials, Furniture and furnishings, Cleaning and safety. EPA CPDat classifies this chemical for functional uses including pH regulating agent, Chelating agent, Cleaning agent.
US
FDA
Route: BUCCAL; Dosage form: GUM, CHEWING; Maximum daily exposure: 720 mg
US
FDA
Pretzel Crisps Original
Snack Factory
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.
Route: BUCCAL; Dosage form: TABLET; Maximum daily exposure: 20 mg
US
FDA
Route: INFILTRATION; Dosage form: INJECTION; Potency: ADJ PH
US
FDA
Route: INTRA-ARTERIAL; Dosage form: INJECTION, SOLUTION; Potency: ADJ PH
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION; Potency: 32.4 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: 630 mg
US
FDA
Route: INTRAVASCULAR; Dosage form: INJECTION; Potency: ADJ PH
US
FDA
Route: INTRAVASCULAR; Dosage form: INJECTION, SOLUTION; Potency: ADJ PH
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION; Potency: 241 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SOLUTION; Maximum daily exposure: 1248 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Maximum daily exposure: 1247 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Potency: ADJ PH
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Potency: 0.01 %w/v
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 90 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Potency: 6 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, FOR SUSPENSION; Maximum daily exposure: 39 mg
US
FDA
Route: ORAL; Dosage form: GUM, CHEWING; Maximum daily exposure: 240 mg
US
FDA
Route: ORAL; Dosage form: LOZENGE; Maximum daily exposure: 500 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION; Maximum daily exposure: 48 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 90 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EFFERVESCENT; Maximum daily exposure: 430 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 80 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 30 mg
US
FDA
Route: ORAL; Dosage form: TROCHE; Maximum daily exposure: 375 mg
US
FDA
Route: SUBCUTANEOUS; Dosage form: INJECTION; Potency: ADJ PH
US
FDA
Route: SUBLINGUAL; Dosage form: TABLET; Maximum daily exposure: 8 mg
US
FDA
FDA NDC lists this ingredient in 106 active drug products and 114 total products.
US
FDA
openFDA substance registry classifies this ingredient as chemical.