The FDA is initiating a process to potentially remove prescription fluoride products, such as drops and tablets, designed for use in children. This move is prompted by ongoing discussions regarding optimal fluoride levels and potential risks associated with excessive fluoride intake during early childhood. While fluoride is known to strengthen tooth enamel and prevent cavities, concerns exist about the possibility of fluorosis, a condition that can cause discoloration of teeth due to overexposure.
The FDA's review will consider current scientific evidence and expert opinions on the appropriate use of fluoride supplements in children. The agency is seeking to balance the benefits of fluoride in preventing tooth decay with the potential risks of overexposure. The decision-making process will involve a thorough evaluation of available data and public input.
This proposal does not affect fluoride toothpaste or fluoridated community water supplies, which are regulated separately. Parents and caregivers are encouraged to consult with their dentists and pediatricians to determine the most appropriate fluoride regimen for their children, considering individual needs and risk factors.
FDA Considers Removing Prescription Fluoride for Children
The Food and Drug Administration (FDA) is proposing to withdraw approval for prescription fluoride drops and tablets intended for children. This action follows concerns about potential overexposure to fluoride and its effects on dental health. The proposal aims to ensure the safe and appropriate use of fluoride supplements in young children. Experts are weighing in on the potential benefits and risks of this decision.
Source: Read the original article at CBS