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Clarification of When Products Made or Derived from Tobacco are Regulated as Drugs, Devices, or Combination Products - Amendments to Regulations (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library

Clarification of When Products Made or Derived from Tobacco are Regulated as Drugs, Devices, or Combination Products - Amendments to Regulations (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library presents the complete text of the Clarification of When Products Made or Derived from Tobacco are Regulated as Drugs, Devices, or Combination Products - Amendments to Regulations (US Food and Drug Administration Regulation) (FDA) (2018 Edition). Updated as of May 29, 2018 The Food and Drug Administration (FDA) is issuing this final rule to describe the circumstances in which a product made or derived from tobacco that is intended for human consumption will be subject to regulation as a drug, device, or a combination product under the Federal Food, Drug, and Cosmetic Act (the FD& C Act). This action is intended to provide direction to regulated industry and to help avoid consumer confusion. This book contains: - The complete text of the Clarification of When Products Made or Derived from Tobacco are Regulated as Drugs, Devices, or Combination Products - Amendments to Regulations (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section