Cosmetic Regulations, Labeling and Safety

Cosmetic products are expected to only exert superficial, not physiological, effects on the human body, meaning they can make no claims that imply treatment of medical conditions or that affect structure or function of the body. Raw materials used as ingredients in cosmetics are also, by law, considered cosmetics. While the FDA is developing mandatory Good Manufacturing Practice (GMP) regulations, anticipated in 2026, the industry is expected to follow best standards and practice and to maintain a good safety track record.

This seminar will help you understand the laws and regulations allowing you to deliver the safe, high quality personal care products consumers demand.

What are legally acceptable formats for the package? How about ingredients, including color additives? What kinds of claims can be made for cosmetics products and how should their labeling and packaging be designed accordingly? How can GMPs be instilled when little prescriptive guidance is currently available?