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FDA bans red dye No. 3
Now that the FDA has banned red dye No. 3, what about more common food dyes?
Following the ban of red dye No. 3 in the United States, experts weigh in on the potential health risks of red dye No. 40, yellow No. 5 and others.
FDA ban on dye Red 3 sparks calls for more food safety reform: "It's about time"
Red 3, often used in cakes, candies and drinks to achieve a bright cherry-red color, has long been criticized for its health risks.
What Foods Will Be Impacted by FDA’s Ban on Red Dye No. 3—And What Could Replace It
T he U.S. Food and Drug Administration (FDA) banned the use of Red Dye No. 3 in food and ingested drugs on Wednesday, more than three decades after the agency prohibited it from being used in cosmetics because of possible cancer risks.
COVID, Rfk Jr. and FDA
RFK Jr. petitioned FDA in 2021 to revoke authorization of all COVID vaccines
Robert F. Kennedy Jr., who's nominated to become the next health secretary, asked the federal government to revoke its authorization of all COVID-19 vaccines in May 2021, just as vaccinated Americans began returning to a sense of normalcy after pandemic lockdowns.
RFK Jr. Asked FDA to Nix COVID Vaccine During Pandemic
Vaccine skeptic and nominee to be Donald Trump’s secretary of the Department of Health and Human Services, Robert F. Kennedy, Jr., asked the Food and Drug Administration to pull authorization for all COVID-19 vaccines in May 2021,
RFK Jr. Tried to Kill the Covid Vaccine When It Was Needed Most
Trump's pick to lead the Department of Health and Human Services petitioned the FDA over the shot that saved thousands of lives
AstraZeneca, Datroway and US FDA
US FDA approves AstraZeneca's drug for breast cancer
The U.S. Food and Drug Administration has approved AstraZeneca and partner Daiichi Sankyo's precision drug to treat a type of breast cancer, the health regulator said on Friday. The treatment, jointly developed with the Japanese company,
AstraZeneca’s Datroway approved in U.S. for HER2-negative breast cancer patients
DXd, has been approved in the US for the treatment of adult patients with unresectable or metastatic hormone receptor HR-positive, HER2-negative breast cancer who have received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease.
AstraZeneca Gets FDA Approval for Metastatic Breast Cancer Treatment Datroway
AstraZeneca said the U.S. Food and Drug Administration approved Datroway, a treatment for metastatic breast cancer developed in combination with Daiichi Sankyo. The Anglo-Swedish drugmaker on Friday said that the approval is for adult breast cancer patients who have received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease.
FDA floats plan to make cigarettes nonaddictive
FDA moves to cut nicotine from cigarettes, in plan first floated under Trump
Zeller credited Gottlieb for advocating for the nicotine regulation within the Trump White House, after the Obama administration had fallen short. Obama officials had promised Zeller they would back rules to curb nicotine and menthol.
FDA floats plan to make cigarettes nonaddictive, but its fate rests with Trump
The Biden administration is floating a long-awaited proposal to make cigarettes less addictive by capping their nicotine levels
FDA proposes caps on nicotine in cigarettes
The FDA has proposed caps on nicotine in cigarettes. The potential rule could reduce the concentration of nicotine in cigarettes by more than half.
FDA 'Closely Monitoring' ZYN Nicotine Pouches
FDA OKs sales of Zyn nicotine pouches, citing health benefits for adult smokers
Federal health officials on Thursday backed the public health benefits of nicotine pouches, authorizing Philip Morris International’s Zyn to help adult smokers cut back or quit cigarettes.
FDA authorizes Zyn nicotine pouches, cites lower risk than cigarettes
The FDA authorized the marketing of 20 Zyn products on Thursday, marking the first allowance for the fast-growing nicotine pouches.
Philip Morris Gains Competitive Edge with FDA Authorization of ZYN Nicotine Pouches
Analyst Matthew Smith of Bank of America Securities maintained a Buy rating on Philip Morris (PM – Research Report), with a price target of
3h
on MSN
FDA orders manufacturers to do a better job detecting bird flu in raw pet food
FDA wants pet food manufacturers to do a better job identifying possible signs of bird flu in raw foods such as uncooked meat ...
1d
Yogurt Recall Update As FDA Sets Risk Level Over Plastic Contamination
Greek yogurt has been recalled because it may contain foreign objects, given the FDA's second-most severe risk level.
11h
Califf concludes 2nd FDA stint
FDA Commissioner Robert Califf is closing the book on his second stint leading the agency that regulates products accounting ...
11h
on MSN
Outgoing FDA chief flags online weight loss drug dangers
By Ahmed Aboulenein WASHINGTON (Reuters) -Current laws and regulations are not enough to protect Americans from the risks of ...
10h
on MSN
FDA's Suggested Change to Food Packaging Raises Concerns Among Experts
Newsweek spoke to experts about the FDA's suggestion to place nutrition information on the front of packaged foods.
Healio
10h
FDA approves therapies for colorectal cancer, mantle cell lymphoma
The FDA approved two oncology regimens on Jan. 16.One is for a subset of patients with colorectal cancer and the other for ...
The American Journal of Managed Care
11h
FDA Grants 2 Traditional Approvals for Acalabrutinib
The Bruton tyrosine kinase inhibitor was approved in combination with bendamustine and rituximab in previously untreated ...
13h
on MSN
FDA make major ban on key ingredient in Americans' most nostalgic foods
FDA bans an ingredient used in many American-favorite foods and beverages, here are the ones that didn't make the cut.
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