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FDA Approves ‘Spravato’ Nasal Spray
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 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 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
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.
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.
A popular skincare product is part of nationwide FDA recall. Do you have this moisturizer?
The U.S. Food and Drug Administration has issued a recall on a popular skin moisturizer that's available nationwide. Do you have this product?
19h
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 ...
4h
on MSN
The FDA Issued a Class II Recall on Nearly 20,000 Cases of Horizon Organic Milk
In January, the FDA reclassified an existing Horizon Organic milk recall as a Class II, which the agency says "may cause ...
1d
on MSN
FDA warns of serious allergic reactions with some multiple sclerosis drugs
The U.S. Food and Drug Administration on Wednesday warned about the risk of a rare but serious allergic reaction with the use ...
16h
on MSN
FDA bans Red 3 dye from food and drugs. A scientist explains the artificial color's health risks and long history
Red 3—also called FD&C Red No. 3, erythrosine or E127—has been widely used in food, cosmetics and pharmaceuticals since its ...
2d
FDA makes key decision on Zyn nicotine pouches
In a statement, the FDA said it has authorized the marketing and sale of Philip Morris International’s Zyn nicotine pouches.
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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