# STRAWBERRY

URL: https://app.greenveil.ai/ingredients/ingredient_unii_4_j2_ty8_y81_v
Categories: pharma
Identifier: drug bank:DB10571

> STRAWBERRY. Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Potency: 20 mg/5ml Assessed from 8 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Potency: 20 mg/5ml

## Regulatory status

- US: inactive ingredient database — Route: ORAL; Dosage form: POWDER, FOR SUSPENSION; Potency: 20 mg/5ml
- US: inactive ingredient database — Route: ORAL; Dosage form: SOLUTION; Maximum daily exposure: 6 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: SUSPENSION; Maximum daily exposure: 21 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: SYRUP; Potency: 2.5 mg/5ml
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, ORALLY DISINTEGRATING; Potency: 1 mg
- US: marketed drug occurrence — FDA NDC lists this ingredient in 5 active drug products and 5 total products.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as structurallydiverse.

_Assessed by Greenveil._