The adrenergic antagonist improved near vision in adults with presbyopia, with over 20 hours of improvement from a single ...

The U.S. Food and Drug Administration recalled more than 3.1 million bottles of eye drops sold at CVS, Walgreens and other ...

Several common cough drop brands are being pulled from shelves after officials raised concerns about how they were made.

A California company has recalled more than 3.1 million bottles of lubricating eye drops because it had not properly tested – ...

Reproxalap was found to be safe to take in patients diagnosed with dry eye disease (DED), as no serious treatment-emergent ...

The U.S. Food and Drug Administration (FDA) has classified a nationwide recall of multiple cough drop products as a Class II ...

More than 3 million eye drop bottles were recalled nationwide due to potential sterility issues across many store-brand products. FDA labeled it Class II, meaning serious health risks are unlikely and ...

Eye drops sold at grocery stores and pharmacies across the country were recalled because they may not be sterile and may therefore pose an infection risk. Pocket-size 15 mL bottles were recalled from ...

April 3 (UPI) --More than three million bottles of eye drops sold at stores across the United States have been recalled by their manufacturer because they may not be sterile. K.C. Pharmaceuticals ...

Millions of eye drop products have been recalled over concerns they may not be sterile, according to an enforcement report from the U.S. Food and Drug Administration. And many of the brands were sold ...

A pharmaceutical company has issued a voluntary recall of over 3 million of its over-the-counter eye-drop products after the Food and Drug Administration cited a “lack of assurance of sterility.” ...