Final answer:
The Florida Food Drug and Cosmetic Act is subject to regulations set by the Federal Food, Drug, and Cosmetic Act, as enforced by the FDA. The FDA oversees a broad range of products from drugs to cosmetics to foods with varying degrees of regulation. Other related legislation such as the FDAAA of 2007 further extends the FDA's authority.
Step-by-step explanation:
The Florida Food Drug and Cosmetic Act (FFDCA) is a set of laws that govern the oversight and regulations for food, drugs, and cosmetics within the state of Florida. However, permits and regulations are largely determined by the overarching Federal Food, Drug, and Cosmetic Act (FD&C Act), which was first enacted in 1938 and has undergone extensive amendments since. The U.S. Food and Drug Administration (FDA) is the federal agency responsible for enforcing the FD&C Act, ensuring the safety and efficacy of drugs, regulating the labeling and safety of cosmetics, and overseeing the quality of foods.
The FDA's regulatory programs are diverse and cover a wide range of products. For instance, the FDA enforces standards for prescription drugs that include testing, manufacturing, labeling, advertising, marketing, and safety, while its regulation of cosmetics primarily focuses on labeling and safety. All color additives in cosmetics must receive FDA approval before being used in products sold in the U.S. The FDA also regulates foods, food additives, dietary supplements, and various other categories using specific standards and enforcements tailored to each category.
It's important to note that the FDA's regulatory scope extends beyond these categories under the authority granted by related legislation, such as the Public Health Service Act and parts of the Controlled Substances Act. The Food and Drug Administration Amendments Act (FDAAA) of 2007 is another critical piece of legislation that amended the FD&C Act, granting additional authorities and responsibilities to the FDA.