date:Sep 20, 2012
f the available process that the FDA can implement if it desires to take action against a company for using an ingredient that the FDA perceives to be dangerous. Such actions may extend to more common ingredients for which the FDA believes there is inadequate evidence of safety. Is this the avenue that the FDA will use to regulate caffeine in energy drinks sold as supplements? If a company leaves the door open for the FDA by mixing the representations of its products as supplements and beverages