What are the FDA regulations for caffeine added to food supplements?

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What are the FDA regulations for caffeine added to food supplements?

What are the FDA regulations for caffeine added to food supplements? 

The FDA (Food and Drug Administration) has established regulations for adding caffeine to food supplements in the United States. The FDA considers caffeine a “dietary ingredient” and regulates its use in dietary supplements under the Dietary Supplement Health and Education Act of 1994 (DSHEA). 

Under DSHEA, dietary supplements containing caffeine must be labelled accurately and include information on the total amount of caffeine per serving, the serving size, and any other ingredients. Additionally, the label must include a statement indicating that the product contains caffeine and should not be used by individuals sensitive to caffeine or who have underlying medical conditions without consulting a healthcare professional. 

The FDA does not have specific limits on the amount of caffeine that can be added to dietary supplements. Still, it requires that the amount of caffeine is safe for human consumption and not act as a risk for any significant or unreasonable injury or disease. 

In addition to labelling requirements, the FDA also monitors the safety of dietary supplements containing caffeine and can take enforcement actions against products that are found to be adulterated or misbranded. The FDA also guides the safe use of caffeine in dietary supplements, including recommendations on daily limits and warnings for specific populations, such as pregnant or breastfeeding women, children, and individuals with heart or other medical conditions [1]. 

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