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FDA Proposes New Testing Rules
FDA proposes new tests to detect asbestos in cosmetics and other products containing talc
The proposed rule is required under a law passed by Congress last year, and is intended to ensure the safety of makeup and baby powder.
FDA proposes rule to target asbestos in talc cosmetic products
The U.S. Food and Drug Administration (FDA) has proposed a new rule to require standardized testing of talc-containing cosmetics for asbestos, a known carcinogen linked to serious illnesses.
FDA proposes new testing rules to ensure cosmetics are asbestos-free
The Food and Drug Administration is proposing a rule that cosmetic companies would have to take extra steps to ensure that any products containing talc are free of asbestos.
FDA recalls eye drops
Systane eye drops recalled due to fungal contamination: FDA
One lot of Systane Lubricant Eye Drops Ultra PF, manufactured by Alcon Laboratories, has been recalled due to fungal contamination, the FDA announced this week.
FDA Announces Nationwide Eye Drops Recall Due to Fungal Contamination
Systane eye drops were recalled earlier this week after the company discovered a fungal contamination in one of its products.
Eyedrops recalled due to possible 'life-threatening' fungal contamination
A popular household brand of eye drops has been recalled after a ‘potentially life-threatening’ fungal contamination was discovered. Alcon Laboratories told users on December 21 to ‘immediately’ stop using Systane Lubricant Eye Drops from one lot after a consumer complaint.
FDA, Opdivo and Bristol Myers Squibb
FDA approves injectable version of Bristol Myers Squibb's cancer drug Opdivo
The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's blockbuster cancer drug, Opdivo.
Bristol-Myers Squibb : FDA Approves Opdivo Qvantig For Subcutaneous Use In Adult Solid Tumors
Bristol Myers Squibb (BMY) announced Friday that the U.S. Food and Drug Administration has approved Opdivo Qvantig (nivolumab and
Bristol-Myers gets FDA okay for injectable Opdivo
The FDA has reportedly approved an injectable formulation of Bristol-Myers Squibb's (NYSE:BMY) oncology drug Opdivo. Previously, the PD-1 inhibitor drug was only available through IV infusion. The injectable formulation,
FDA Elevates Costco Egg Recall to Class 1
FDA escalates recall of Costco eggs to include risks of 'severe illness or death'
There were approximately 10,800 retail units of the affected eggs sold at 25 Costco stores in five states beginning on Nov. 22.
Recalled Costco eggs may cause severe illness due to salmonella, FDA warns in new alert
Federal food regulators raised their alarm for recalled eggs sold from Costco stores over possible salmonella exposure, reclassifying the targeted product to its highest risk level.
Food Recall Update: Class 1 Alert Issued for Costco Eggs Linked to Salmonella
Approximately 10,800 retail units of the eggs were distributed to 25 Costco stores starting Nov. 22, but the recall was initially issued on Nov. 27 after the company found that eg
22h
on MSN
Hair Spray Recall in 12 States As FDA Issues Risk Warning
Dichloromethane, a volatile solvent commonly used in industrial applications, has been banned in products in many areas, ...
Scientific American
16h
The FDA Is Changing What Foods Can Be Called ‘Healthy’
Whole grains and fruits are in, and added sugar is out. That’s going to change what’s on a lot of cereal boxes and other things ...
1d
FDA Approves Generic GLP-1 Medicine For Diabetes Treatment
THURSDAY, Dec. 26, (2024 HealthDay News) -- The U.S. Food and Drug Administration (FDA) announced on Monday the approval of ...
10h
on MSN
Prebiotic Supplement Recall in 25 States As FDA Issues Risk Warning
Customers who purchased the supplement are advised to discontinue use immediately and inspect their product to identify if it ...
Everyday Health
15h
FDA Approves First Medication for Obstructive Sleep Apnea
By aiding weight loss, Zepbound can improve symptoms of obstructive sleep apnea (OSA) in people with obesity — but CPAP ...
1d
on MSN
Startup led by Seattle doctors gets FDA approval for virus-killing, surgical mask technology
Seattle's Singletto is ramping up sales of surgical masks treated with its virus-killing technology and exploring other ...
Hosted on MSN
1d
FDA Says Decongestant in Many Cold Medicines Doesn't Work. So What Does?
Changes are coming to the cold and cough aisle of your local pharmacy: U.S. officials are moving to phase out the leading ...
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