The Food and Drug Administration is moving closer to allowing a new sunscreen ingredient that is already used overseas. It’s called bemotrizinol.

FDA is considering adding bemotrizinol, a sunscreen ingredient used abroad for decades, to U.S. products for broader UV ...

Sanofi’s Qfitlia and Cablivi approved in China, expanding care for rare diseases Qfitlia, the first antithrombin-lowering therapy for hemophilia, can offer consistent protection with as few as six ...

A new law is intended to speed up introduction of advanced sunscreens in the United States The U.S. has fallen behind other ...

Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., ...

The U.S. Food and Drug Administration has approved an updated label for Unloxcyt (cosibelimab-ipdl) for the treatment of ...

From Beauty of Joseon and Round Lab, many of the globally popular K-beauty brands share a history, having started as small ...

“It was a really hard sell,” recalls Druker, an oncologist and CEO of the Oregon Health & Science University Knight Cancer Institute, decades on. There were seemingly valid concerns at the time, he ...

Studies in the early 2000s claimed there were major risks associated with HRT. The Food and Drug Administration said Monday it will remove the "black box" warning from hormone replacement therapy (HRT ...

U.S. sunscreens don’t contain Tinosorb S or BEMT, found in European sunscreens and which gives you better protection. The FDA is reviewing the issue. Dreamstime/TNS TNS When it comes to sunscreen, the ...

The FDA has rejected Biohaven’s request for approval of a neurological disorder therapy, prompting the biopharma to reprioritize its pipeline in order to shrink its annual R&D spend by 60%. After a ...

The Food and Drug Administration (FDA) is launching an effort to streamline the approval process for cheaper alternative “biosimilar” versions of biologic drugs as a way to curb health costs. The ...