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Regulatory status of caffeine in the United States

2014/10/01 by L. Rosenfeld, Jeremy J. Mihalov, Susan J. Carlson +1 · 3 citations
Chemistry · Engineering · Medicine · Psychology · #Business #Caffeine #Chemistry #Coffee research and impacts #Drug #Eating Disorders and Behaviors #Environmental health #Food and drug administration #Food science #Green IT and Sustainability #Ingredient #Medicine #Pharmacology

paper · pdf · doi:10.1111/nure.12136

openalex publication_date 2014/10/01 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/15

Abstract

This article summarizes the history of the regulation of caffeine, a key component of caffeine-containing energy drinks and other caffeine-containing energy products, in the United States. Caffeine as an ingredient in food has been regulated by the US Food and Drug Administration (FDA) since 1958, when the Food Additives Amendment to the Federal Food, Drug and Cosmetic Act was enacted. It is listed as a substance that is generally recognized as safe by experts for its intended use in cola-type beverages at levels not to exceed 200 parts per million. Here, the history of FDA evaluations of the safe use of, as well as consumer exposure to, caffeine in food in the United States is outlined. Finally, the FDA's current concerns about caffeine and caffeine-containing energy products are reported, along with the current activities to address those concerns.

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