The FDA is phasing out synthetic food dyes—here's what it means for your family's health
In a sweeping move that puts children's well-being front and center, the U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) just announced a prominent plan to phase out petroleum-based synthetic dyes from the nation's food supply. For parents who've long worried about mysterious color-coded ingredients in their child's favorite snacks, this marks a long-overdue victory for transparency and health.
For decades, American families have unknowingly been consuming artificial dyes—FD&C Red No. 40, Yellow No. 5, and Blue No. 1, to name a few—added to everything from cereals and candies to juices and baked goods. These synthetic additives, made from petrochemicals, offer no nutritional benefit and have been linked to a range of health concerns, especially in children. Think hyperactivity, allergic reactions, and even potential long-term impacts on development.
'Some food producers have been feeding Americans petroleum-based chemicals without their knowledge or consent,' said HHS Secretary Robert F. Kennedy, Jr. 'That era is coming to an end.'
Related: Baked goods FDA recall: what you need to know about the 2 million products impacted
The FDA's new measures are part of the Biden administration's broader 'Make America Healthy Again' initiative, and here's what you need to know:
Two dyes—Citrus Red No. 2 and Orange B—will have their authorization revoked in the coming months.
Six more widely used synthetic dyes (like Red No. 40 and Yellow No. 5) will be eliminated by the end of next year.
Natural alternatives such as butterfly pea flower extract and gardenia blue are being fast-tracked for approval.
The deadline for phasing out Red No. 3 (found in candies and baked goods) has been moved up.
The FDA is working with the NIH to deeply study the connection between additives and children's health.
While European countries and Canada have already restricted or replaced synthetic dyes in many foods, the U.S. has lagged behind. That means American children have been exposed to additives banned elsewhere for safety reasons. The shift now underway acknowledges mounting research—and parental concern—about the role these dyes may play in the rise of childhood issues like obesity, depression, and ADHD.
As FDA Commissioner Dr. Marty Makary stated, 'Given the growing concerns of doctors and parents… we should not be taking risks.'
This policy shift is a game-changer, but food industry reform won't happen overnight. In the meantime, there are steps you can take:
Read labels: Look out for ingredients labeled as 'FD&C' followed by a color and number.
Choose natural options: Many brands now use fruit or vegetable-based colorings.
Make your voice heard: Continue advocating for clean ingredients by supporting brands and stores committed to transparency.
Model mindful eating: This is a great opportunity to talk to your kids about what's in their food and why it matters.
For many families, this announcement isn't just about dyes—it's about reclaiming trust in the food system. It's about knowing that what we feed our children supports not only their bodies, but also their focus, energy, and emotional health.
This change signals that when parents speak up, when science is prioritized, and when the health of our littlest citizens is placed at the forefront, meaningful change is possible.
Let's keep demanding better. Because our kids deserve nothing less.
Related: FDA sets new limits on lead in baby food—what parents need to know
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
27 minutes ago
- Yahoo
These Popular Eggs Are Being Recalled Over Salmonella Risk
If you've been living for your morning sunny-side eggs…well, brace yourself. The August Egg Company—the parent behind Sunnyside, Clover, Raley's, and a few other brands—is recalling a whopping 1.7 million dozen eggs due to a potential salmonella outbreak. Yep, it's serious.. The U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention have flagged the August Company's 'brown cage-free and brown certified organic egg' for possible contamination, meaning you might want to double-check that carton in your fridge before cracking it open. If you didn't know, Salmonella is that sneaky bacteria behind food poisoning and can cause anything from mild stomach upset to serious illness. These eggs were shipped to Walmart stores and other grocers in nine states: California, Washington, Nevada, Arizona, Wyoming, New Mexico, Nebraska, Indiana, and Illinois. They have a best-by date from March 4 to June 19 and food codes P-6562 or CA5330. Not sure if your eggs are on the list? The FDA has a full rundown of all the recalled brands you can check out. And if the cartons in your fridge match any of the food codes or best-by-dates, toss them out immediately. While it's somewhat okay to eat an egg past its expiration date, this isn't the case. The FDA has already connected a current salmonella outbreak to the eggs. As of now, a total of 79 cases have been reported in seven states, while 21 people have been hospitalized. We get it: eggs are pricey, and tossing them feels like a waste. But don't risk it. Plus, most places will give you a full refund. And if your eggs touched any surfaces, wipe those down like your life depends on it. If after eating you feel dizzy, nauseous, or get a fever—don't play it cool. Call your doctor. This is serious business. Trust me, as a four-time survivor of food poisoning, you don't want to take any chances. You Might Also Like Insanely Easy Weeknight Dinners To Try This Week 29 Insanely Delicious Vodka Cocktails
Yahoo
3 hours ago
- Yahoo
AG pushes back on federal abortion medication restrictions
BOSTON (SHNS) – Attorney General Andrea Campbell implored federal regulators Thursday to eliminate medication abortion restrictions on prescribers and pharmacies, arguing Massachusetts already has 'robust' guardrails in place to protect patient safety. Campbell, along with AGs from California, New York and New Jersey, want the U.S. Food and Drug Administration to eliminate its Risk Evaluation and Mitigation Strategy (REMS) program for mifepristone — or at least stop applying certain parts of it to the four petitioning states. The program outlines certification requirements for health care providers and pharmacies to dispense mifepristone, plus paperwork that patients must sign. About 65% of abortions in Massachusetts in 2023 were medication abortions, according to the 64-page citizen petition Campbell co-filed Thursday. The FDA says REMS programs are used for drugs with 'serious safety concerns to help ensure the benefits of the medication outweigh its risks.' Campbell's office contends the mifepristone requirements impose 'burdensome restrictions on access to medication abortion while not meaningfully improving patient safety, and that these restrictions severely impede patient access by reducing the number of prescribers and pharmacies authorized to dispense this FDA-approved medication.' 'The Mifepristone REMS Program also imposes an undue burden on pregnant patients experiencing miscarriage and early pregnancy loss who seek treatment at emergency departments,' the petition says. 'For instance, the administrative requirements imposed by the REMS can effectively discourage emergency departments from carrying mifepristone in their pharmacies.' Reduced access to mifepristone can particularly impact patients in rural and medically underserved areas, the petition added. The Democratic AGs teamed up in response to U.S. Health and Human Services Secretary Robert Kennedy recently instructing FDA Commissioner Martin Makary to pursue a 'complete review' of mifepristone and labeling requirements. The FDA is required to respond to their petition within 180 days by either approving, denying or dismissing it — or providing a 'tentative response' about why the agency is unable to reach a decision yet, according to federal regulations. In response to the Trump administration, Beacon Hill lawmakers are escalating their focus on shoring up protections for reproductive and transgender care. A Sen. Cindy Friedman bill (S 2522) that's gaining traction would tighten the 2022 abortion shield law, including by requiring hospitals to provide emergency abortion care and allowing provider practices, rather than specific prescriber names, to appear on medication abortion labels. WWLP-22News, an NBC affiliate, began broadcasting in March 1953 to provide local news, network, syndicated, and local programming to western Massachusetts. Watch the 22News Digital Edition weekdays at 4 p.m. on Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

4 hours ago
Ukraine war veteran runs 5k one week after receiving a prosthetic leg
ABC News' Chief Global Affairs Correspondent Martha Raddatz reports on a new American-run rehabilitation center in Kyiv.