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Which Decongestants Are Effective? Why the FDA Wants to Pull a Popular Medicine Ingredient
Phenylephrine is included in many cold and flu products, but a scientific panel last year found that it doesn't really do its job at "unstuffing" when taken by mouth.
FDA wants to pull decongestant found in many cold, allergy medicines
The FDA is proposing the removal of phenylephrine, a popular nasal decongestant, in oral form from over-the-counter use. Here’s why.
FDA moves to pull popular decongestant from shelves amid effectiveness concerns
The US Food and Drug Administration announced a proposal to remove oral phenylephrine – a common ingredient in many popular over-the-counter decongestants – from the market, citing evidence that it doesn’t work.
What is oral phynylephrine and why does the FDA want to remove it from cold medicine?
Oral phenylephrine is used in over-the-counter products like Sudafed and Dayquil to help temporarily relieve the common symptom of colds and allergies. Phenylephrine has been sold for more than 75 years, predating the agency’s own regulations on drug effectiveness.
FDA proposes to end use of decongestant found in cold meds
The Food and Drug Administration has proposed ending the use of a common ingredient found in many popular over-the-counter cold and allergy medications.
FDA to pull common but ineffective cold medicine from market
The FDA says oral phenylephrine, used in many over-the-counter cough and cold medicines, "is not effective as a nasal decongestant."
FDA proposes ending use of decongestant found in many cold, allergy medicines
An extensive review determined that the ingredient, oral phenylephrine, doesn’t actually relieve nasal congestion.
FDA proposes pulling ineffective cold medicine from shelves
When you're feeling under the weather, you likely grab your go-to cough and cold medicine. But are all the ingredients helping you fight off that cold?
FDA wants to ban decongestant found in cold, allergy medicine
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Four Major Cold, Allergy Meds May Get Pulled Because They Don't Work
Ugh, that explains it! No wonder so many of us never felt better. More than 80 million people across the country deal with seasonal allergies. That’s 25 percent of the United States according to the Center for Disease Control,
FDA Claims Ingredients In Cold Medicines Is Ineffective
FDA Claims Ingredients In Cold Medicines Is Ineffective
39m
on MSN
Drinking Water Recall As FDA Sets Risk Level
West Virginia-based Berkeley Club Beverages, Inc. has voluntarily recalled more than 150,000 bottles of water as they may contain coliform bacteria. The products have now been given a Class III risk ...
MLive
18h
FDA cinnamon recall: Throw away these 11 products
The U.S. Food and Drug Administration (
FDA
) is urging people to not consume some cinnamon products due to unsafe levels of ...
2d
RFK Jr. Gloats About Plan to Gut FDA Under Trump
Donald Trump associate and noted health nut Robert F. Kennedy Jr. still has federal health regulators in his crosshairs. On ...
pharmaphorum
11h
Autolus bags FDA approval for leukaemia cell therapy
Autolus has picked up its first product approval, getting an
FDA
green light for Aucatzyl as a treatment for patients with ...
Dallas Morning News on MSN
3d
FDA adds new warning to weight loss drugs including Wegovy
The FDA is warning that patients taking GLP-1s may be at a higher risk of inhaling fluid into their lungs while under ...
Fortune on MSN
3d
RFK Jr. is expected to join Trump’s government after warning the ‘FDA’s war on public health is about to end,’ telling all employees to ‘pack your bags’
Kennedy Jr. has been a vaccine skeptic, sometimes a conspiracy theorist, and he might just be a part of president-elect ...
2d
Don’t throw out expired COVID-19 tests, FDA says
If your rapid COVID-19 tests have reached their expiration dates, don't toss them just yet. Here's how to find out if their ...
1d
This is the dietary supplement that the FDA has recalled because of its banned ingredient
The Food and Drug Administration (FDA) has recently issued a recall for two dietary supplements, ZoomMax and ZapMax, due to ...
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