FTC Rules
- Business Opportunity Rule
- The FTC’s Proposed Business Opportunity Rule and How It Affects MLM Marketers
Food, Drug, and Cosmetic Act (21 CFR Chapter 9)
Chapter II – Definitions
Chapter III – Prohibited Acts and Penalties
Chapter V – Drugs and Devices
- Part A – Drugs and Devices
- Part B – Drugs for Rare Diseases or Conditions
- Part C – Electronic Product Radiation Control
Chapter VII – General Authority
- Part A – General Administrative Provisions
- Part B – Colors
- Part C – Fees
- FOIA Fees
- Drug Fees Chapter VIII – Imports and ExportsChapter IX – Miscellaneous
Commercial Practices
- Disclosure Requirements and Prohibitions Concerning Franchising and Business Opprotunity Ventures
- Cooling-Off Period for Door-to-Door Sales
Bioterrorism Preparedness and Response Act of 2002
- Final Rule: Registration of Food Facilities Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002
- Compliance Policy Guide Guidance for FDA Staff Registration of Food Facilities Under the Public Health Security and Bioterrorism Preparedness and Response Act
Cosmetics
- Cosmetic Labeling Regulations
- Title 21, Code of Federal Regulations Cosmetic Products
- Cosmetic Good Manufacturing Practice Guidelines
Food & Dietary Supplements
- Guidance for Industry: Factors that Distinguish Liquid Dietary Supplements from Beverages, Considerations Regarding Novel Ingredients, and Labeling for Beverages and Other Conventional Foods (December 7, 2009)
- Final Rule 21 CFR Part 101: Regulations on Statements Made for Dietary Supplements Concerning the Effect of the Product on the Structure or Function of the Body (Effective February 7, 2000)
- Dietary Supplement Final Rules (September 23, 1997)
- Food Labeling Regulation, Amendments; Food Regulation Uniform Compliance Date; and New Dietary Ingredient Premarket Notification
- Food Labeling; Requirements for Nutrient Content Claims, Health Claims, and Statements of Nutritional Support for Dietary Supplements
- Food Labeling; Nutrient Content Claims: Definition for “High Potency” and Definition of “Antioxidant” for Use in Nutrient Content Claims for Dietary Supplements and Conventional Foods
- Food Labeling; Notification Procedures for Statements on Dietary Supplements
- Premarket Notification for a New Dietary Ingredient
- Summary of Dietary Supplement Health and Education Act of 1994
- Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Dietary Supplements; Proposed Rule
- FDA/CFSAN Current GMP in Manufacturing, Packing or Holding Human Food (21 CFR Part 110)
- Iron-Containing Supplements and Drugs: Label Warning Statements and Unit-Dose Packaging Requirements; Final Rule. Also available in PDF format.
- New RDIs (Reference Daily Intakes) for Vitamin K, Chloride, Chromium, Maganese, Molybdenum, and Selenium
- FDA Definition for High Potency Claim and Definition of Antioxidant Use in Nutrient Content Claims
