# FD&C BLUE NO. 2

URL: https://app.greenveil.ai/ingredients/ingredient_unii_l06_k8_r7_dqk
Categories: pharma
Identifier: cfr:21 CFR 74.102

> FD&C BLUE NO. 2. Route: BUCCAL; Dosage form: TABLET; Potency: 0.01 mg Assessed from 13 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: Route: BUCCAL; Dosage form: TABLET; Potency: 0.01 mg

## Regulatory status

- US: inactive ingredient database — Route: BUCCAL; Dosage form: TABLET; Potency: 0.01 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 4 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE, DELAYED RELEASE; Potency: 0.22 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE, EXTENDED RELEASE; Maximum daily exposure: 4 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 25 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, CHEWABLE; Maximum daily exposure: 3 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, COATED; Potency: 24.12 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, DELAYED RELEASE; Potency: 0.2 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Potency: 2.78 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 2 mg
- US: inactive ingredient database — Route: TOPICAL; Dosage form: SOAP; Potency: NA
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as mixture.

_Assessed by Greenveil._