The FDA, under Robert Kennedy's leadership, announced plans to remove ingestible fluoride supplements from the market. This move contrasts with recommendations from the CDC, ADA, and AAP, which support fluoride's role in preventing tooth decay. Fluoride, added to public water since the 1940s, benefits nearly 75% of Americans. Kennedy has criticized fluoridation efforts and aims to eliminate fluoride by November 2024. The FDA's claims regarding fluoride's health risks are largely unsubstantiated and question the effectiveness of supplements, which remain unregulated by the agency.
The FDA's statement, led by Robert Kennedy, initiates the removal of ingestible fluoride supplements, challenging longstanding recommendations from various health organizations regarding dental health.
This decision contradicts not just the FDA's own history but also the consensus of prominent health authorities who advocate for fluoride's protective benefits against tooth decay.
Kennedy's FDA highlights unsubstantiated claims linking fluoride to health issues, including thyroid disorders and decreased IQ, while supplements remain unregulated by FDA standards.
The administration's move represents a significant policy shift, with implications for children's dental care and public health debates surrounding fluoride use.
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