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 1768 composition records across product categories including Construction and building materials, Furniture and furnishings, Laboratory supplies.
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 BICARBONATE in our catalog (epa_cpdat).
Products
1,768
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 1768 composition records across product categories including Construction and building materials, Furniture and furnishings, Laboratory supplies. EPA CPDat classifies this chemical for functional uses including pH regulating agent, Chelating agent, Abrasive.
US
FDA
Route: BUCCAL; Dosage form: GUM, CHEWING; Maximum daily exposure: 240 mg
US
FDA
Deocreme mit Natron und Zink
Balea
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: BUCCAL; Dosage form: TABLET; Maximum daily exposure: 42 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION; Maximum daily exposure: 175 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: 1000 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Potency: ADJ PH
US
FDA
Route: INTRAPERITONEAL; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: ADJ PH
US
FDA
Route: INTRATHECAL; Dosage form: INJECTION; Potency: 0.05 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION; Potency: 812 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SOLUTION; Maximum daily exposure: 3219 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SUSPENSION; Maximum daily exposure: 160 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Maximum daily exposure: 3059 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Maximum daily exposure: 52 mg
US
FDA
Route: INTRAVITREAL; Dosage form: INJECTION; Potency: 0.18 %w/v
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 320 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 4 mg
US
FDA
Route: ORAL; Dosage form: FILM, SOLUBLE; Maximum daily exposure: 2 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, EFFERVESCENT; Potency: 267 mg
US
FDA
Route: ORAL; Dosage form: GUM, CHEWING; Maximum daily exposure: 360 mg
US
FDA
Route: ORAL; Dosage form: LOZENGE; Maximum daily exposure: 100 mg
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SOLUTION; Potency: 1250 mg/100ml
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE; Potency: 140 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Potency: 10.6 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Potency: 30 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EFFERVESCENT; Maximum daily exposure: 57600 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 81 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 86 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Maximum daily exposure: 107 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE; Maximum daily exposure: 6 mg
US
FDA
Route: RESPIRATORY (INHALATION); Dosage form: SOLUTION; Potency: 2 %w/w
US
FDA
Route: SUBCUTANEOUS; Dosage form: INJECTION; Potency: ADJ PH
US
FDA
Route: SUBLINGUAL; Dosage form: TABLET; Maximum daily exposure: 6 mg
US
FDA
Route: VAGINAL; Dosage form: INSERT; Maximum daily exposure: 129 mg
US
FDA
FDA NDC lists this ingredient in 223 active drug products and 250 total products.
US
FDA
openFDA substance registry classifies this ingredient as chemical.
US
USDA FoodData Central
Observed in 1 USDA branded foods including 1 LITER BOTTLE VICHY WATER.