# VANILLIN

URL: https://app.greenveil.ai/ingredients/ingredient_dtxsid_dtxsid0021969
Categories: beauty, cleaning, food, industrial, pharma
Functions: Deodorizer, Dye, Flavouring and nutrient, Fragrance, antimicrobial adhesion agent
Identifier: DTXSID0021969

> VANILLIN is used as deodorizer / dye. EPA CPDat observed this chemical in 1152 composition records across product categories including Cleaning products and household care, Vehicle, Personal care. Assessed from 23 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: EPA CPDat observed this chemical in 1152 composition records across product categories including Cleaning products and household care, Vehicle, Personal care.

## Regulatory status

- US: commercial use observed — EPA CPDat observed this chemical in 1152 composition records across product categories including Cleaning products and household care, Vehicle, Personal care. EPA CPDat classifies this chemical for functional uses including Fragrance, Deodorizer, Flavouring and nutrient.
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE; Potency: 0.94 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Potency: 0.94 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: ELIXIR; Potency: NA
- US: inactive ingredient database — Route: ORAL; Dosage form: LIQUID; Potency: NA
- US: inactive ingredient database — Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Potency: 2 mg/1ml
- US: inactive ingredient database — Route: ORAL; Dosage form: SOLUTION; Potency: 2.5 mg/5ml
- US: inactive ingredient database — Route: ORAL; Dosage form: SUSPENSION; Maximum daily exposure: 6 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: SYRUP; Potency: NA
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 12 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, CHEWABLE; Potency: 2.5 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, COATED; Potency: 65.5 mg
- 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; Potency: 3.4 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 5 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, FILM COATED, EXTENDED RELEASE; Maximum daily exposure: 1 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Potency: 0.26 mg
- US: inactive ingredient database — Route: TOPICAL; Dosage form: OINTMENT; Potency: NA
- US: marketed drug occurrence — FDA NDC lists this ingredient in 10 active drug products and 10 total products.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as chemical.

_Assessed by Greenveil._