Soapmaking 101 with the Soap Queen
All the fundamentals of making cold process soap from scratch with lye and oil; make all natural sustainable soap from scratch for yourself of start a side hustle selling soap.
Understanding FDA Cosmetic vs. Drug Claims
In episode 92 of Soapmaking 101 with the Soap Queen, Anne-Marie Faiola dives into the complexities of FDA regulations as they pertain to soapmaking. The episode starts with a warm welcome and an overview of the topic, followed by a detailed discussion on the FDA's definitions for cosmetics, drugs, and soap. Anne-Marie explains how these definitions impact soapmakers, highlighting the importance of understanding advertising and labeling requirements. She also shares resources to help navigate FDA regulations effectively. The episode wraps up with a sponsor message from BrambleBerry.com, providing essential information for soapmakers aiming to comply with legal standards.
Key Points
- Understanding the Food and Drug Administration's definitions of cosmetics, drugs, and soap is crucial for proper product labeling and marketing.
- A product can be classified as both a drug and a cosmetic if it has dual intended uses, such as dandruff shampoo that both cleanses and treats dandruff.
- Soap is regulated by the Consumer Product Safety Commission unless it is marketed for beautifying or altering appearance, which would then classify it under the Food and Drug Administration's jurisdiction.
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Transcript
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