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Prescription Fluoride Faces FDA Scrutiny Despite Widespread Support From Providers and the Public

UNITED STATES, JUL 23 – The FDA is assessing prescription fluoride supplements amid safety concerns including potential neurodevelopmental effects and debates on their benefits for children without fluoridated water.

  • On July 23, the FDA and Regan-Udall Foundation held a public meeting with 18 experts to weigh a potential ban on fluoride tablets and drops.
  • The FDA plans to remove these unapproved prescription fluoride supplements for children by October 31 due to safety concerns, amid states banning public water fluoridation.
  • Fluoride has been added to US water since 1945 for cavity prevention, but declining fluoride prescriptions and recent bans in Utah and Florida have increased debate about access and choice.
  • Supporters, including the American Academy of Pediatrics and Health Secretary Kennedy, emphasize choice and warn removing supplements without alternatives could worsen oral health for children in non-fluoridated areas.
  • The FDA will complete its safety review by October 31 and allow public comments, signaling the decision will balance risks and benefits while continuing fluoride discussions after the ban.
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Orthodontic Products broke the news in on Tuesday, July 22, 2025.
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