Dietary Supplement Labeling Compliance
What you'll gain from this course
It is up to dietary supplement manufacturers to ensure their supplement labels are compliant before they go to market, and the regulations can be confusing and difficult to interpret. Label noncompliance can cause your product to be considered misbranded and subject to Food & Drug Administration (FDA) or Federal Trade Commission (FTC) regulatory action.
The course is interactive, with hands-on exercises. Bring your questions and prepare to interact with the instructor and your peers in the industry.
Learning Outcomes
In this course, you will learn about the regulations that govern dietary supplement labeling, including:
- What can be considered a dietary supplement
- Label compliance/noncompliance
- Regulations that govern dietary supplements
- Supplement facts formatting
- Ingredient lists
- Permitted claims, enforcement/litigation trends
- Adverse event reporting
- Regulatory background and enforcement
- Mandatory label elements
- Voluntary label elements
- How to apply the FTC and FDA regulations
- Defining a dietary supplement
Who Should Attend
NSF’s labeling compliance course for dietary supplements is suitable for:
- Management
- Marketing
- Quality control/assurance
- Packaging
- Sales
- Laboratory operations
- Product development
- Suppliers and distributors
- Regulatory affairs
- Legal
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