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FDA-Approved Nasal Spray For Depression Is 1st Of Its Kind
FDA approves standalone use of J&J’s ketamine-derived depression treatment
The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression, the company said on Tuesday.
FDA approves Johnson & Johnson’s ketamine-derived nasal spray for depression as stand-alone treatment
The announcement was welcome news for those with major depressive disorder, which affects an estimated 8.3% of the adult population.
FDA approves first-of-its-kind nasal spray for severe depression
Johnson & Johnson has announced the FDA’s approval of a first-of-its-kind, esketamine nasal spray called Spravato for the standalone treatment of major depressive disorder (MDD), PTSD, and similar psychiatric conditions.
Popular face moisturizer sold nationwide recalled, FDA says
Face Moisturizer Recalled Nationwide as FDA Sets Risk Level
On December 23, First Aid Beauty recalled 2,756 jars of its Ultra Repair Cream. According to the FDA, a deviation from Current Good Manufacturing Practice regulations—which are essential to ensure the safety and efficacy of pharmaceutical products—was the reason for the recall.
Popular face moisturizer sold nationwide recalled, FDA says
The recall, which is ongoing, includes 2,756 jars of the cream, which were distributed nationwide, according to an enforcement report from the Federal Drug Administration. The recall was initiated on Dec. 23, 2024, with email notifications sent out to distributors and buyers. No press release was issued.
Popular face moisturizer recalled nationwide
A popular face moisturizer sold by First Aid Beauty has been recalled nationwide after some jars of the cosmetic cream that weren't meant to be sold were unintentionally distributed. The FDA has classified the recall as a Class II,
Scientific American
2h
What’s in ZYN, the FDA-Authorized Nicotine Pouch? Is It Harmful?
ZYN, the popular brand of flavored nicotine pouches, recently earned FDA authorization for reducing smoking, but some ...
3h
on MSN
Dip Recall Update as FDA Sets Risk Class
The spinach artichoke dip mix was recalled due to it having been underprocessed, the Food and Drug Administration said.
Rolling Out
1h
FDA unveils 8 critical safety measures for berry industry
FDA introduces comprehensive safety measures targeting norovirus and hepatitis A in fresh and frozen berries, addressing ...
1d
Federal regulations paused, halting FDA's proposed ban on formaldehyde in hair products
Over the years, an increasing number of studies have linked formaldehyde to cancers that are especially prevalent among Black ...
2d
on MSN
FDA proposes mandatory front-of-package nutrition labels to combat spike in chronic diseases
The U.S. Food and Drug Administration (FDA) is demanding increased, in-your-face food transparency when it comes to nutrition ...
2h
on MSN
FDA releases update on chicken broth recall at Ga. Walmarts
The Food and Drug Administration has released an update on a recall for chicken broth sold at Georgia Walmarts.
Sun Star
18m
FDA warns public against unregistered dried mango product
THE Food and Drug Administration (FDA) warned the public on Friday, January 24, 2025, about the presence of an unregistered dried mango product on the market.In ...
STAT
3d
Three former FDA officials: Here’s what Trump and his nominees need to know
The FDA is the leading science-based consumer protection agency in the world. Three former senior officials write about what ...
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