# SODIUM PHOSPHATE, DIBASIC

URL: https://app.greenveil.ai/ingredients/ingredient_dtxsid_dtxsid0064969
Categories: pharma
Identifier: DTXSID0064969

> SODIUM PHOSPHATE, DIBASIC. EPA DSSTox provides the canonical identifier, structure, and synonym profile for this chemical. Assessed from 18 sources.

## Safety assessment

- Chemical concern: not yet assessed
- Rationale: EPA DSSTox provides the canonical identifier, structure, and synonym profile for this chemical.

## Regulatory status

- US: inactive ingredient database — Route: INTRADERMAL; Dosage form: INJECTION; Potency: 0.2 %w/v
- US: inactive ingredient database — Route: INTRAMUSCULAR; Dosage form: INJECTION; Potency: 40 mg
- US: inactive ingredient database — Route: INTRAMUSCULAR; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: 40 mg
- US: inactive ingredient database — Route: INTRAVENOUS; Dosage form: INJECTION; Potency: 200 mg
- US: inactive ingredient database — Route: INTRAVENOUS; Dosage form: INJECTION, POWDER, FOR SOLUTION; Potency: 40 mg
- US: inactive ingredient database — Route: OPHTHALMIC; Dosage form: SUSPENSION; Potency: 0.43 %w/w
- US: inactive ingredient database — Route: ORAL; Dosage form: CONCENTRATE; Potency: 17 mg/5ml
- US: inactive ingredient database — Route: ORAL; Dosage form: FILM, SOLUBLE; Maximum daily exposure: 9 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: SOLUTION; Potency: 40 mg/1ml
- US: inactive ingredient database — Route: ORAL; Dosage form: SYRUP; Maximum daily exposure: 70 mg
- US: inactive ingredient database — Route: ORAL; Dosage form: TABLET, EXTENDED RELEASE; Maximum daily exposure: 143 mg
- US: inactive ingredient database — Route: SUBCUTANEOUS; Dosage form: INJECTION; Maximum daily exposure: 14 mg
- US: inactive ingredient database — Route: SUBCUTANEOUS; Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION; Potency: 2.98 mg
- US: inactive ingredient database — Route: TOPICAL; Dosage form: CREAM; Potency: 0.1 %w/w
- US: marketed drug occurrence — FDA NDC lists this ingredient in 17 active drug products and 18 total products.
- US: listed in openFDA substance — openFDA substance registry classifies this ingredient as mixture.

_Assessed by Greenveil._