Alcon Laboratories recalled one lot of Systane Lubricant Eye Drops Ultra PF ... presence of undeclared metformin and glyburide. These prescription drugs can lead to serious side effects such ...

DATROWAY® (datopotamab deruxtecan-dlnk) has been approved in the U.S. for the treatment of adult patients with unresectable or metastatic hormone receptor (HR) positive, HER2 negative (IHC 0, IHC 1+ ...

I use the expensive lubricant eye drops for moisture — I've used Visine ... A bottle of sulfate-free biotin shampoo that rivals the $$ prescription versions — thousands of reviewers swear ...

Advise patients to use preservative-free lubricant eye drops several times daily for prophylaxis ... development and commercialization of prescription medicines in Oncology, Rare Diseases and ...

Fort Worth, Texas-based Alcon Laboratories has voluntarily recalled one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, which are packaged in batches of 25.

The eye drops, Systane Lubricant Eye Drops Ultra PF, are single vial drops available in a 25-count box and manufactured by Alcon Laboratories, based in Fort Worth, Texas. "Alcon evaluated a ...

The Food and Drug Administration (FDA) announced Monday that Alcon Laboratories, based out of Texas, is voluntarily recalling a single lot of “Systane Lubricant Eye Drops Ultra SPF, Single Vials ...

Systane eye drops have been recalled due to potential fungal contamination, the U.S. Food and Drug Administration announced. The recall affects one lot of Systane Lubricant Eye Drops Ultra PF ...

Fort Worth, Tx.-based Alcon Laboratories has voluntarily recalled one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, which are packaged in batches of 25. The recall comes ...

A popular brand of eye drops is being recalled nationwide due to a possible contamination, which may cause vision damage, according to the Food and Drug Administration (FDA). On Monday, the FDA ...

The affected packages of Systane Lubricant Eye Drops Ultra PF Single Vials On-the-Go were recalled after a customer complaint of "foreign material observed inside a sealed single use vial," the ...