# .ALPHA.-TOCOPHEROL

URL: https://app.greenveil.ai/ingredients/ingredient_unii_h4_n855_pnz1
Categories: pharma
Identifier: cfr:21 CFR 310.546

> .ALPHA.-TOCOPHEROL. Route: BUCCAL; Dosage form: FILM, SOLUBLE; Potency: 0.07 mg Assessed from 14 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: Route: BUCCAL; Dosage form: FILM, SOLUBLE; Potency: 0.07 mg

## Regulatory status

- US: inactive ingredient database — Route: BUCCAL; Dosage form: FILM, SOLUBLE; Potency: 0.07 mg
- US: inactive ingredient database — Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SUSPENSION; Potency: 0.64 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: CAPSULE; Maximum daily exposure: 16 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: SOLUTION; Potency: 1.05 mg/1ml
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET; Maximum daily exposure: 2 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, CHEWABLE; Potency: 0.1 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 4 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, FILM COATED; Maximum daily exposure: 246 mg
- US: inactive ingredient database — Route: TOPICAL; Dosage form: OINTMENT; Potency: NA
- US: inactive ingredient database — Route: TOPICAL; Dosage form: SYSTEM; Potency: 0.1 mg
- US: marketed drug occurrence — FDA NDC lists this ingredient in 18 active drug products and 20 total products.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as mixture.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as concept.

_Assessed by Greenveil._