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 1957 composition records across product categories including Specialty occupational products, Raw materials, Food and drug.
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 POVIDONE K30 in our catalog (epa_cpdat).
Products
1,957
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 1957 composition records across product categories including Specialty occupational products, Raw materials, Food and drug. EPA CPDat classifies this chemical for functional uses including anti-irritant, Film former, Anti-static agent.
US
FDA
Route: AURICULAR (OTIC); Dosage form: SUSPENSION; Potency: NA
US
FDA
Sport Triumph
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: INTRAMUSCULAR; Dosage form: INJECTION; Potency: 0.2 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Potency: 1.8 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION; Potency: 1.8 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION/ DROPS; Potency: 0.6 %w/v
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 300 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED PELLETS; Potency: 10.03 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED, EXTENDED RELEASE; Potency: NA
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Potency: NA
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE PELLETS; Maximum daily exposure: 32 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 56 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, FOR SUSPENSION, EXTENDED RELEASE; Potency: NA
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Potency: 35 mg/5ml
US
FDA
Route: ORAL; Dosage form: SOLUTION; Maximum daily exposure: 3000 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION; Potency: 20 mg/5ml
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 216 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE; Maximum daily exposure: 48 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Potency: 49.2 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 53 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 101 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Potency: 240 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED, EXTENDED RELEASE; Potency: 17 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FOR SUSPENSION; Potency: 2 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Potency: 15.03 mg
US
FDA
Route: SUBCUTANEOUS; Dosage form: IMPLANT; Potency: 6 mg
US
FDA
Route: TOPICAL; Dosage form: SYSTEM; Maximum daily exposure: 41 mg
US
FDA
Route: TRANSDERMAL; Dosage form: FILM, EXTENDED RELEASE; Potency: NA
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION; Maximum daily exposure: 648 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: 0.2 %w/v
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Maximum daily exposure: 600 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, SUSPENSION; Potency: 0.08 %w/v
US
FDA
Route: INTRAVENOUS; Dosage form: SOLUTION, CONCENTRATE; Maximum daily exposure: 1000 mg
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 173 mg
US
FDA
Route: SUBCUTANEOUS; Dosage form: INJECTION; Potency: 20 mg
US
FDA
Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Potency: 20 mg
US
FDA
Route: SUBCUTANEOUS; Dosage form: INJECTION, SUSPENSION; Potency: 0.5 %w/v
US
FDA
Route: SUBCUTANEOUS; Dosage form: SUSPENSION; Potency: 0.5 %w/v
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 200 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 90 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 67 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, FOR SUSPENSION; Potency: 0.27 mg
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Maximum daily exposure: 126 mg
US
FDA
Route: ORAL; Dosage form: SOLUTION; Potency: 500 mg/5ml
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 640 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE; Potency: 0.45 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Maximum daily exposure: 240 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 49 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 200 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 163 mg
US
FDA
Route: BUCCAL; Dosage form: TABLET; Maximum daily exposure: 1 mg
US
FDA
Route: INTRAMUSCULAR; Dosage form: INJECTION; Potency: 0.59 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Maximum daily exposure: 42 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Maximum daily exposure: 4 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION; Maximum daily exposure: 14 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 540 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, COATED, EXTENDED RELEASE; Maximum daily exposure: 15 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 227 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE PELLETS; Maximum daily exposure: 178 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 120 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, LIQUID FILLED; Maximum daily exposure: 101 mg
US
FDA
Route: ORAL; Dosage form: GRANULE; Maximum daily exposure: 202 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, EFFERVESCENT; Potency: 40 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, FOR SUSPENSION; Maximum daily exposure: 120 mg
US
FDA
Route: ORAL; Dosage form: LOZENGE; Maximum daily exposure: 700 mg
US
FDA
Route: ORAL; Dosage form: PELLET; Maximum daily exposure: 24 mg
US
FDA
Route: ORAL; Dosage form: POWDER; Maximum daily exposure: 378 mg
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SOLUTION; Maximum daily exposure: 2832 mg
US
FDA
Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Maximum daily exposure: 257 mg
US
FDA
Route: ORAL; Dosage form: SOLUTION; Maximum daily exposure: 300 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION; Maximum daily exposure: 148 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION, EXTENDED RELEASE; Maximum daily exposure: 474 mg
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 2828 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE; Maximum daily exposure: 245 mg
US
FDA
Route: ORAL; Dosage form: TABLET, CHEWABLE, EXTENDED RELEASE; Maximum daily exposure: 12 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Maximum daily exposure: 160 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 516 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE PARTICLES; Maximum daily exposure: 70 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 368 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 245 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED, EXTENDED RELEASE; Potency: 45 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FOR SUSPENSION; Maximum daily exposure: 462 mg
US
FDA
Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Maximum daily exposure: 71 mg
US
FDA
Route: ORAL; Dosage form: TROCHE; Maximum daily exposure: 175 mg
US
FDA
Route: SUBLINGUAL; Dosage form: FILM; Maximum daily exposure: 7 mg
US
FDA
Route: SUBLINGUAL; Dosage form: TABLET; Maximum daily exposure: 30 mg
US
FDA
Route: TOPICAL; Dosage form: AEROSOL, FOAM; Potency: 1.9 %w/w
US
FDA
Route: TRANSDERMAL; Dosage form: FILM, EXTENDED RELEASE; Maximum daily exposure: 16 mg
US
FDA
Route: TRANSDERMAL; Dosage form: SYSTEM; Maximum daily exposure: 15 mg
US
FDA
Route: VAGINAL; Dosage form: INSERT; Maximum daily exposure: 147 mg
US
FDA
Route: AURICULAR (OTIC); Dosage form: SOLUTION/ DROPS; Maximum daily exposure: 2 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION; Potency: 0.3 %w/v
US
FDA
Route: OPHTHALMIC; Dosage form: SOLUTION/ DROPS; Potency: 1.2 %w/w
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION; Maximum daily exposure: 4 mg
US
FDA
Route: OPHTHALMIC; Dosage form: SUSPENSION/ DROPS; Potency: 1.5 %w/v
US
FDA
Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 270 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 137 mg
US
FDA
Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 118 mg
US
FDA
Route: ORAL; Dosage form: GRANULE, FOR SUSPENSION; Maximum daily exposure: 140 mg
US
FDA
Route: ORAL; Dosage form: SUSPENSION; Maximum daily exposure: 2 mg
US
FDA
Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 966 mg
US
FDA
Route: ORAL; Dosage form: TABLET, COATED; Potency: 9.77 mg
US
FDA
Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 192 mg
US
FDA
Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 498 mg
US
FDA
Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 128 mg
US
FDA
Route: TOPICAL; Dosage form: SOLUTION; Maximum daily exposure: 120 mg
US
FDA
Route: TOPICAL; Dosage form: SYSTEM; Maximum daily exposure: 280 mg
US
FDA
Route: TRANSDERMAL; Dosage form: SOLUTION; Maximum daily exposure: 100 mg
US
FDA
Route: TRANSDERMAL; Dosage form: SYSTEM; Potency: 20 mg
US
FDA
FDA NDC lists this ingredient in 53 active drug products and 54 total products.
US
FDA
openFDA substance registry classifies this ingredient as polymer.
US
FDA
openFDA substance registry classifies this ingredient as mixture.