Class I

Drug Recall: Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.33 FL OZ (10 mL) bottles, Distributed by Cardinal Health Dublin, Ohio 43017, NDC 70000-0088-1

Kilitch Healthcare India Limited · November 13, 2023

Reason for Recall

Non-Sterility

Distribution

Nationwide within the United States

States Affected

NATIONWIDE

Quantity Affected

12,960 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0295-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Kilitch Healthcare India Limited Drug Recall: Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.33 FL OZ (10 mL) bottles, Distributed by Cardinal Health Dublin, Ohio 43017, NDC 70000-0088-1 | SafeCheck