Abstract
The Food and Drug Administration (FDA) has been more proactive in regulating sunscreen products. In 2011, the FDA publicized a set of new requirements for marketing over-the-counter sunscreens in the United States. The primary goal of the new FDA requirements was to provide consumers with a clear understanding of the level of protection actually provided by a sunscreen. Furthermore, information about protection against ultraviolet A radiation, associated with early aging and skin cancer, was to be clarified. With the new regulations, sunscreen products that provide protection against ultraviolet A and ultraviolet B would be allowed to be marketed as broadspectrum sunscreen [1]. © 2013 by the article author(s).
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Haydar, K., & Burkhart, C. G. (2013). Sunscreen regulations and use of anti-inflammatory agents in sunscreens. Dermatology Online Journal. Dermatology Online Journal. https://doi.org/10.5070/d3197018969
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