Food and Drug Administration FDA

FDA, sunscreen

FDA proposes new sunscreen active ingredient, fulfilling MAHA promise and AOC goal

Sunscreen in the United States is about to get a long-awaited glow-up with the Food and Drug Administration’s decision to approve a new ingredient that has been used in other countries for years. The FDA announced a proposal on Thursday to approve the ingredient bemotrizinol,

· 8h · on MSN

FDA proposes allowing sunscreen ingredient already used in Europe and Asia

· 7h · on MSN

FDA proposes use of new sunscreen ingredient already allowed abroad

FDA expands COVID vaccine probe to adult deaths

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· 2d

FDA Examines Possible Adult Deaths From Covid Shots in Probe

The Food and Drug Administration is investigating whether Covid-19 vaccines caused deaths in adults, as part of a safety review that earlier appeared to just be focused on children.

· 1d · on MSN

FDA to investigate possible COVID vaccine deaths in 'multiple age groups'

Wellbeing Whisper on MSN · 14h

FDA expands COVID vaccine probe to adult deaths amid policy turmoil

Tri-State Livestock News

FDA Conditionally Approves Topical Drug for Cattle for New World Screwworm and Cattle Fever Tick

Today, the U.S. Food and Drug Administration conditionally approved Exzolt Cattle-CA1 (fluralaner) topical solution for the ...

Medical Marketing & Media

Two new Untitled Letters, multiple close-outs: Latest on FDA’s pharma ad crackdown

More recently, the FDA posted two two letters: one backdated for September 9, regarding GSK’s HIV medication Apretude and one ...

7hon MSN

US FDA approves first at-home device for depression

The U.S. Food and Drug Administration has approved Flow Neuroscience's at-home brain stimulation device to treat depression, ...

Long Island Press on MSN

The breakthrough drug transforming HIV prevention: FDA-approved lenacapavir protects with twice-yearly injections

The U.S. Food and Drug Administration (FDA) recently approved a groundbreaking new option for preventing HIV, the virus that ...

2don MSN

FDA opens safety review of injectable RSV drugs approved for babies and toddlers

Food and Drug Administration officials have opened a safety review of two injectable drugs used to protect babies and ...

2don MSN

US FDA approves first drug under new fast-track review program

The U.S. Food and Drug Administration approved on Tuesday the first drug under its new fast-track program designed to shorten ...

10hon MSN

Cheese Recall Sparks Highest FDA Risk Warning

Vulnerable groups such as pregnant women, older people and those with weakened immune systems are most at risk.

STAT

FDA staff fear Tracy Beth Høeg will bring bias and instability to embattled drug center

WASHINGTON — In 2008, Tracy Beth Høeg, then a resident physician and ultramarathon runner, expressed dismay at vice presidential candidate Sarah Palin’s denial of climate change.

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