FDA moves to take prescription fluoride supplements off the market
- On Tuesday, U.S. Health regulators announced plans to phase out prescription fluoride supplements for children, citing safety concerns about these ingestible products.
- This effort follows rising legal challenges and an investigation by Texas Attorney General Ken Paxton into fluoride toothpaste marketing as misleading and deceptive.
- FDA Commissioner Marty Makary highlighted risks including interference with healthy gut bacteria and studies linking excess fluoride intake to reduced IQ in children.
- The FDA stated these supplements were never formally approved and will conduct a scientific review by late October, seeking voluntary product withdrawal from manufacturers.
- Removing these products may take years through a lengthy rulemaking process, aligning with Health Secretary Robert F. Kennedy Jr.'s campaign to reconsider fluoride use amid state-level bans like Utah's.
173 Articles
173 Articles
FDA fluoride ban proposal stuns dentists and scientists amid health concerns
A long-standing dental treatment aimed at preventing cavities in children may soon disappear from the US market, as the Food and Drug Administration (FDA) moves to eliminate fluoride supplements over safety concerns. The agency announced on May 13 that it intends to remove prescription fluoride tablets and drops, citing potential links to altered gut bacteria, thyroid disorders, and lowered IQ. The decision does not affect fluoride in toothpaste…
Fluoride ban a sign of sick government | Letters to the editor
Removing fluoride from our water supply, which for decades dental and medical experts have credited with improving our dental health, will result in mass suffering of millions of children. The cost of dental care for families will soar and there will be lost productivity due to time off to address dental disease. Children will suffer the most, by experiencing unnecessary levels of tooth decay, requiring painful dental procedures. The personal an…
FDA Plans Ban on Kids’ Ingestible Fluoride Drugs - The Southern Maryland Chronicle
SILVER SPRING, Md. — The U.S. Food and Drug Administration announced on May 14, 2025, plans to remove concentrated ingestible fluoride prescription drug products for children from the market, citing potential health risks. Unlike fluoride toothpaste or rinses, these unapproved products, swallowed by infants and toddlers, may disrupt the gut microbiome and are linked to thyroid disorders, weight gain, and possible IQ reduction.“The best way to pr…
Never approved children’s fluoride recalled by FDA but dentists push back
An ingestible fluoride prescription drug product for children was pulled from the market on Tuesday after the Food and Drug Administration (FDA) said it was never approved. The products are known as fluoride tablets, according to NPR. These include drops or lozenges meant for children who don’t get fluoridated water to help prevent cavities.
FDA takes first step to remove fluoride tablets and drops for children from the market
The FDA took steps to remove fluoride drops and pills from the market, saying they have been linked to several adverse health conditions. Dental groups support the use of supplemental fluoride as a safe way to promote oral hygiene, citing studies that show it is 'harmless' at low doses.
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