# FERROSOFERRIC OXIDE

URL: https://app.greenveil.ai/ingredients/ingredient_dtxsid_dtxsid5029639
Categories: industrial, pharma
Functions: Dye, Pigment
Identifier: DTXSID5029639

> FERROSOFERRIC OXIDE is used as dye / pigment. EPA CPDat observed this chemical in 845 composition records across product categories including Raw materials, Construction and building materials, Furniture and furnishings. Assessed from 15 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: EPA CPDat observed this chemical in 845 composition records across product categories including Raw materials, Construction and building materials, Furniture and furnishings.

## Regulatory status

- US: commercial use observed — EPA CPDat observed this chemical in 845 composition records across product categories including Raw materials, Construction and building materials, Furniture and furnishings. EPA CPDat classifies this chemical for functional uses including Pigment, Dye.
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 11 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE, COATED; Potency: 0.11 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Maximum daily exposure: 6 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Potency: 1.49 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Potency: NA
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 2 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, COATED; Potency: NA
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Maximum daily exposure: 6 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 8 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, FILM COATED; Potency: 0.2 mg
- US: marketed drug occurrence — FDA NDC lists this ingredient in 2 active drug products and 2 total products.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as chemical.

_Assessed by Greenveil._