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 7 composition records across product categories including Raw 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 (low) · high confidence.
Prevalence of BORIC ACID in our catalog (fda_ndc).
Products
15
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 7 composition records across product categories including Raw materials. EPA CPDat classifies this chemical for functional uses including pH regulating agent, Biocide, Stabilizing agent.
US
FDA
Route: AURICULAR (OTIC); Dosage form: SOLUTION; Potency: 0.05 %w/w
US
FDA
Talco Bambino para niños
Roldan
Route: AURICULAR (OTIC); Dosage form: SUSPENSION; Potency: 0.6 %w/v
US
FDA
Route: AURICULAR (OTIC); Dosage form: SUSPENSION/ DROPS; Maximum daily exposure: 3 mg
US
FDA
Route: BUCCAL; Dosage form: MOUTHWASH; Potency: 7.36 mg/1ml
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Potency: 0.53 %w/v
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SOLUTION; Maximum daily exposure: 210 mg
US
FDA
Route: OPHTHALMIC; Dosage form: DROPS; Potency: 1 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: EMULSION; Potency: 0.3 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: GEL; Potency: 0.5 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Maximum daily exposure: 60 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION, GEL FORMING, EXTENDED RELEASE; Potency: 0.3 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Maximum daily exposure: 48 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION; Maximum daily exposure: 12 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION/ DROPS; Maximum daily exposure: 22 mg
US
FDA
Route: TOPICAL; Dosage form: EMULSION; Potency: 1.3 %w/w
US
FDA
Route: TOPICAL; Dosage form: SUSPENSION/ DROPS; Potency: 0.3 %w/v
US
FDA
FDA NDC lists this ingredient in 13 active drug products and 15 total products.