Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP).
[1] It is divided into three chapters: Most of the Chapter I regulations are based on the Federal Food, Drug, and Cosmetic Act.
The 1000 series covers radiation-emitting device (e.g. cell phones, lasers, x-ray generators); requirements enforced by the Center for Devices and Radiological Health.
The 1100 series includes updated rules deeming items that statutorily come under the definition of "tobacco product" to be subject to the Federal Food, Drug, and Cosmetic Act as amended by the Tobacco Control Act.
[5] The 1200 series consists of rules primarily based in laws other than the Food, Drug, and Cosmetic Act: Notable sections: