Federal Regulations

Business Opportunity Notice of Proposed Rulemaking

The FTC's Proposed Business Opportunity Rule and How It Affects MLM Marketers

Chapter I - Short Title Chapter II - Definitions Chapter III - Prohibited Acts and Penalties Chapter IV - Food 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 VI - Cosmetics Chapter VII - General Authority Part A - General Administrative Provisions Part B - Colors Part C - Fees FOIA Fees Drug Fees Chapter VIII - Imports and Exports Chapter IX - Miscellaneous

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

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