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    ‘No Artificial Colors’ May Not Mean What You Think Under New FDA Policy

    The change is meant to allow food manufacturers that don’t use potentially harmful “petroleum-based” dyes to promote the fact. But it leaves open the possibility that the claim could be used on products with other concerning colors.

    Colorful candy
    Brightly colored candy often contains artificial food dyes.
    Photo: Getty Images

    The Food and Drug Administration recently announced that it is redefining the label “No Artificial Colors” on food packaging. The policy change is part of an agency-wide effort to incentivize food companies to move away from using what many refer to as "petroleum-based" dyes or certified color additives—such as FD&C Blue No. 2 and Yellow No. 5—and toward colors from natural sources.

    Under the current administration, the FDA has approved six such color options. These additives differ from FD&C (food, drug, and cosmetic) certified dyes used to make thousands of food and drink products more brightly colored and visually appealing. Last year, more than 20 state legislatures introduced bills to ban the use of certified color additives or require products containing them to carry a warning label, following research linking their consumption to adverse neurobehavioral effects in some children

    More on Additives and Other Substances in Food

    Under longstanding FDA policy, all color additives have been considered artificial for labeling purposes, regardless of source, meaning only products with no added colors could claim to be free of artificial dyes. But in a letter to manufacturers on Thursday, the agency said companies can use the term “no artificial colors” on labels of products that contain any coloring agents, except for the FD&C certified colors.

    “On the surface, it may sound like a good plan,” says Michael Hansen, PhD, a senior staff scientist at Consumer Reports. “But the policy will make it even more challenging for people to understand what’s in their food. It’s really just giving the industry another way to confuse consumers.”

    Dozens of other color additives fall outside the policy’s scope, including titanium dioxide—a synthetically produced white pigment banned as a food additive in the European Union over genotoxicity concerns—chemically synthesized beta-carotene, and colors produced using genetically engineered yeast or bacteria, such as soy leghemoglobin.

     “The policy is too broad and could be abused in ways that mislead or confuse consumers, many of whom will assume that ‘no artificial colors’ means either no color at all or that the food was colored only with plant- and animal-derived colorings,” said Sarah Sorscher, director of regulatory affairs at the Center for Science in the Public Interest.

    How Color Additives Are Regulated

    The FDA’s announcement follows the administration’s April 2025 pledge to phase out certified color additives from the American food supply by the end of 2026—a commitment that has yet to be backed up by any regulatory directive and relies largely on voluntary industry cooperation. 

    The timeline already appears to be slipping: On its website tracking industry pledges, the FDA now states that it is working to eliminate six certified color additives from the food supply by the end of 2027, a full year past the administration’s original target.

    “People forget that the administration’s initiative on certified food dyes was not mandated and that it relied on voluntary action by the industry,” said Brian Ronholm, CR’s director of food policy.

    In the absence of binding federal action, states have moved aggressively to restrict certified food dyes on their own. A California law, which goes into effect at the end of 2027, bans six synthetic dyes from food served in the state’s public schools. Meanwhile, even more ambitious legislation passed by West Virginia targets seven dyes in school meals and aims to prohibit the sale of foods containing those dyes statewide in 2028. Other states, including Arizona, Utah, and Virginia, have enacted similar restrictions, many with enforcement mechanisms and civil penalties that go well beyond anything the federal government has proposed. Consumer Reports’ advocacy arm has supported several of those efforts, including California’s landmark Food Safety Act. 

    Notably, the FDA’s recent policy change was implemented through an enforcement discretion letter rather than notice-and-comment rulemaking, meaning that stakeholders and members of the public did not have the opportunity to provide input. 

    “It’s unusual for the FDA to make this kind of policy change through a letter to industry,” said Ronholm. “It almost seems like they were aware that, if they had gone through traditional regulatory channels that included soliciting public comments, they would have been subject to significant criticism for abandoning their commitment to eliminate synthetic dyes.”

    Representatives from the FDA and the International Association of Color Manufacturers did not immediately respond to requests for comment.


    Paris Martineau

    Paris Martineau is an investigative reporter on the special projects team at Consumer Reports. She joined CR in 2025, covering food safety issues and consumer harms. Send her tips and feedback at paris.martineau@consumer.org, or securely via Signal.