U.S. FDA Human Foods Program

U.S. FDA Human Foods Program

6,561 Photos and videos

Tweets

U.S. FDA retweeted

U.S. FDA Human Foods Program @FDAfood

FDA, in collaboration with federal and state partners, is investigating a multistate outbreak of three confirmed or suspected infant botulism illnesses. fda.gov/food/outbreaks-foodb… Do not use any Nara Organics Whole Milk Organic Powdered Infant Formula.

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U.S. FDA

U.S. FDA

@US_FDA

Jun 12

NEWS: FDA cleared for marketing the first over-the-counter (OTC) continuous glucose monitor (CGM) for children. Dexcom Inc.’s Stelo Glucose Biosensor System is an integrated CGM (iCGM) indicated for people two years of age and older who do not use insulin. The milestone is a powerful example of how real-world evidence (RWE) is informing regulatory decisions and supporting innovation – and it reflects our unwavering commitment to developing gold-standard science that protects the public health.

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U.S. FDA

U.S. FDA

@US_FDA

Jun 12

Learn more: fda.gov/news-events/press-an…

FDA Clears First Over-the-Counter Continuous Glucose Monitor for Children

The U.S. Food and Drug Administration today cleared for marketing the first over-the-counter (OTC) continuous glucose monitor (CGM) for children, Dexcom Inc.’s Stelo Glucose Biosensor System, an...

fda.gov

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New World Screwworm Rapid Response

U.S. FDA retweeted

New World Screwworm Rapid Response

@Screwworm_RR

Jun 12

NEWS: The @US_FDA has issued an Emergency Use Authorization for generic Nitenpyram Tablets for the treatment of New World screwworm (NWS) infestations (myiasis) in dogs, puppies, cats, and kittens that weigh at least two pounds and are at least four weeks old. We are working across the federal government to help ensure your pets are protected from screwworm. Read the full release below: fda.gov/news-events/press-an…

FDA Issues Emergency Use Authorization for Generic Over-the-Counter Drug to Treat New World...

FDA today issued an Emergency Use Authorization (EUA) for generic Nitenpyram Tablets (nitenpyram) for the treatment of New World screwworm (NWS) infestations (myiasis) in dogs, puppies, cats, and...

fda.gov

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U.S. FDA

U.S. FDA

@US_FDA

Jun 12

💊 To date, the FDA has approved 87 #Biosimilars—safe and effective options for many chronic conditions—highlighting continued growth in the biosimilars market. 📈 Learn more: fda.gov/drugs/biosimilars/bi….

ALT This image is an infographic from the FDA titled "Biosimilars: what patients need to know." It includes points about biosimilars and their biologic medications, highlighting that they are made from similar sources, have the same treatment risks and benefits, and are safe and effective for many illnesses. It also notes that biosimilars may be more cost-effective than original biologics. The graphic features medical imagery such as an IV bag, syringe, and medicine vial. The FDA logo is at the bottom right.

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U.S. FDA

U.S. FDA

@US_FDA

Jun 11

Today, the FDA issued an emergency use authorization (EUA) for generic nitenpyram tablets, the first generic drug to receive an EUA for the treatment of New World screwworm (NWS) and the first over-the-counter product to treat NWS in dogs, puppies, cats, and kittens. fda.gov/news-events/press-an… @Screwworm_RR

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U.S. FDA

U.S. FDA

@US_FDA

Jun 11

Burnout, depression, stress, anxiety - that stuff is REAL! Guys there is no need to suffer in silence like it’s a badge of honor. Do the right thing and take care of your mind the same way you take care of everything and everyone depending on you. samhsa.gov/mental-health/wha… #MensHealthMonth #MensMentalHealth

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U.S. FDA

U.S. FDA

@US_FDA

Jun 10

FDA is extending the comment period for the Request for Information on Drug Repurposing for Unmet Medical Needs by 30 days — now open until July 11, 2026! federalregister.gov/d/2026-1… Plus, join us for a hybrid public workshop on drug repurposing on August 5 that will cover public docket comments & approaches for prioritizing and selecting repurposing candidates. Stay tuned for registration details. reaganudall.org/news-and-eve…

U.S. FDA

@US_FDA

May 11

FDA is calling on patients, clinicians, and researchers to help identify drugs that could be repurposed to treat chronic and rare diseases and help address other unmet medical needs. Share your ideas to help advance new treatment options. fda.gov/news-events/press-an…

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U.S. FDA

U.S. FDA

@US_FDA

Jun 10

#Biosimilars are safe, effective alternatives to biologic medicines that help expand treatment options for chronic conditions like diabetes, arthritis, heart disease, and prostate cancer. Learn more this #MensHealthMonth. fda.gov/drugs/biosimilars/bi…

ALT A person smiling while using a tablet, seated at a table with a cup and a small plant. The FDA logo is visible in the bottom right corner.

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U.S. FDA

U.S. FDA

@US_FDA

Jun 9

The first new sunscreen active ingredient in 20 years! As the temperatures heat up this summer, FDA is happy to announce expanded options for consumers. Learn more: fda.gov/news-events/press-an…

ALT A person wearing a sunhat and sunglasses holds a child with a yellow hat, who has sunscreen on their face. Both are smiling outdoors on a sunny day. The image includes a text overlay: "FDA expands sunscreen options for the first time in 20 years." The FDA logo is in the top right corner.

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U.S. FDA

U.S. FDA

@US_FDA

Jun 9

FDA continues to strengthen domestic manufacturing, enhance post-market surveillance, and accelerate generic drug reviews to ensure all Americans have access to safe, affordable medications. In our latest FDA Voices blog, learn how our generic drug program is advancing quality, access, and supply chain resilience. fda.gov/news-events/fda-voic…

Ensuring Quality and Access: FDA’s Approach to Generic Drug Oversight

FDA continues to prioritize the speed and efficiency with which generic drugs are regulated, balancing the need for minimizing risk and ensuring access.

fda.gov

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U.S. FDA

U.S. FDA

@US_FDA

Jun 8

Real men get checked. Prostate cancer doesn’t care how young you are, how tough you may feel, or how hard you grind. It will attack any man at any time. Get screened. fda.gov/consumers/health-edu… #MensHealthMonth #ProstateCancerPrevention

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U.S. FDA Recalls

U.S. FDA retweeted

U.S. FDA Recalls

@FDArecalls

Jun 5

Target Recalls Up & Up Fragrance Free and Fresh Cucumber Scented Baby Wipes Due to Potential Microbial Contamination fda.gov/safety/recalls-marke…

9,195

U.S. FDA

U.S. FDA

@US_FDA

Jun 5

With the arrival of New World screwworm in the U.S., veterinarians have questions, and the FDA is here to help. @FDAanimalhealth has published a Dear Veterinarian Letter to help vets identify drugs conditionally approved authorized for NWS and to explain vet legal responsibilities when prescribing drugs for NWS. fda.gov/animal-veterinary/pr…

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U.S. FDA

U.S. FDA

@US_FDA

Jun 5

Protecting animals, farmers, and our food supply remains a top priority for FDA ➡️ fda.gov/animal-veterinary/sa… @Screwworm_RR

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U.S. FDA

U.S. FDA

@US_FDA

Jun 5

Thank you to those who spoke at FDA’s public hearing on the Commissioner's National Priority Voucher (CNPV) pilot program. If you weren’t able to attend, you can view the recording here: youtube.com/live/5gS9gJ99Cvk Didn't comment? There's still time. Submit your public comments by 11:59 PM ET, June 29. regulations.gov/docket/FDA-2…

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U.S. FDA

U.S. FDA

@US_FDA

Jun 4

News Flash! You can’t run on junk food and vibes forever. Energy, focus, mood – it starts with what you eat. Tighten up on what you put in your body. fda.gov/food/nutrition-food-… #MensHealthMonthy #HealtyEating #Nutrition

ALT A person smiles while holding a bowl of salad and cutlery in a fitness area. Text on the image reads "Men's Health Month 2026 #MensHealthMonth," with an FDA logo shown.

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U.S. FDA

U.S. FDA

@US_FDA

Jun 3

FDA is committed to advancing Real-World Evidence use in regulatory submissions across product centers & today updated its list of examples of how RWE has informed FDA's regulatory decisions since 2011. CDRH is now included, along with CDER, CBER & OCE. fda.gov/science-research/rea…

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FDA Biologics

U.S. FDA retweeted

FDA Biologics @FDACBER

Jun 2

Today, the FDA published a draft guidance that when finalized will outline how sponsors can use publicly available information and established platform knowledge to streamline the development of cell and gene therapy products. fda.gov/news-events/press-an…

ALT Grey graphic with text stating "FDA issues draft guidance to streamline development of cell and gene therapy products." The background features multiple faded instances of the words "DRAFT GUIDANCE." The FDA logo is in the bottom right corner.

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FDA Biologics

U.S. FDA retweeted

FDA Biologics @FDACBER

Jun 1

On Thursday June 4, 2026, from 11 am – 12 PM ET, the Office of Therapeutic Products will host a virtual town hall with experts from OTP’s Office of Review Management & Regulatory Review answering questions regarding Biologic License Application readiness. fda.gov/vaccines-blood-biolo…

ALT A graphic for an OTP Town Hall event by the FDA. The topic is "Best Practices for Preparing BLA Submissions for Cell and Gene Therapy Products." Scheduled for Thursday, June 4, 2026, from 11:00 a.m. to 12:00 p.m. ET. The event will be streamed on YouTube, and a recording will be available. The FDA logo is present. No registration is required.

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