“The American Academy of Dermatology Association commends President Bush for signing this bill and recognizing the importance of proper warning labels on indoor tanning equipment,” said Diane R. Baker, MD, FAAD, president of the American Academy of Dermatology Association (Academy). “Demonstrating our commitment to reducing the incidence of and mortality from skin cancer, the Academy worked with congressional leaders to develop this bill,” stated Dr. Baker. “We congratulate bill sponsors Sens. Jack Reed (D-RI) and Johnny Isakson (R-GA) and Reps. Carolyn Maloney (D-NY) and Ginny Brown-Waite (R-FL). Their tireless efforts may ultimately help educate Americans about the health risks of indoor tanning, empowering them to make informed decisions.”
The new law requires the FDA to conduct consumer testing to “determine consumer understanding of label warnings.” It requires the Secretary of Health and Human Services to report back to Congress in one year with the results, including “the measures being implemented by the Secretary to significantly reduce the risks associated with indoor tanning devices.”
“The current labeling on tanning equipment inadequately explains the serious risks associated with indoor tanning,” stated Dr. Baker. “The TAN Act is a first step to correct this and ultimately will help educate the millions of Americans who tan each day about the potential cancer risks associated with ultraviolet (UV) radiation.”
Nearly 30 million people tan indoors in the United States annually. Of these, 2.3 million are teens. Indoor tanning equipment emits ultraviolet radiation which has been declared a known carcinogen by the Department of Health and Human Services. More than 1 million new cases of skin cancer will be diagnosed in the United States this year. Additionally, exposure to UV light is a known risk factor for melanoma, the second most common cancer in women aged 20-29.