Ultraviolet radiation Legislation - Federal Government

To require the Food and Drug Administration to conduct consumer testing to determine the appropriateness of the current labeling requirements for indoor tanning devices and determine whether such requirements provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the skin, including skin cancer, and for other purposes. 2/8/2007--Introduced. Tanning Accountability and Notification Act of 2007 - Requires the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, to determine whether: (1) the labeling requirements for indoor tanning devices provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the eyes and skin, including skin cancer; (2) adding the warning suggested by the American Academy of Dermatology or any other additional warning to the current warning label [...]

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A bill to require the Food and Drug Administration to conduct consumer testing to determine the appropriateness of the current labeling requirements for indoor tanning devices and determine whether such requirements provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the skin, including skin cancer, and for other purposes. 2/16/2007--Introduced. Tanning Accountability and Notification Act of 2007 - Requires the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, to determine whether: (1) the labeling requirements for indoor tanning devices provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the eyes and skin, including skin cancer; (2) adding the warning suggested by the American Academy of Dermatology or any other additional warning to the current warning [...]

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To require the Food and Drug Administration to establish a standard for broad-spectrum protection in sunscreen products, and for other purposes. 7/18/2007--Introduced. Skin Cancer Prevention, Education, and Consumer Right-To-Know Act - Amends the Federal Food, Drug, and Cosmetic Act to deem a drug that is a sunscreen product whose labeling violates this Act to be adulterated.Prohibits the labeling of a drug that is a sunscreen product that fails to meet the standards adopted under this Act from: (1) describing the product using the term "broad-spectrum"; or (2) including a specified symbol adopted to indicate broad-spectrum.Requires the Secretary of Health and Human Services to adopt: (1) a standard for broad-spectrum protection in sunscreen products; and (2) an easily recognized symbol for inclusion in the labeling of sunscreen products meeting such standards.Sets forth minimum standards that the Secretary shall adopt for such broad-spectrum [...]

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To reduce emissions of ozone depleting substances in order to protect the climate and stratospheric ozone layer, and for other purposes. 8/3/2007--Introduced. Global Climate and Ozone Layer Protection Act of 2007 - Expresses the sense of Congress that the United States should negotiate with the other parties to the Montreal Protocol concerning mitigating global warming impacts and accelerating the phaseout of hydrochlorofluorocarbons (HCFCs) for developed and developing countries.Amends the Clean Air Act to allow the production and consumption of class II substances that are used as fire suppression agents for military, commercial aviation, industrial, space, or national security applications and that reduce overall risk to human health and the environment compared to alternatives.Bans the importation of any product manufactured after January 1, 2010, that contains any class II substance that has been phased out of production and consumption for any purpose other [...]

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To reduce emissions of ozone depleting substances in order to protect the climate and stratospheric ozone layer, and for other purposes. 8/3/2007--Introduced. Global Climate and Ozone Layer Protection Act of 2007 - Expresses the sense of Congress that the United States should negotiate with the other parties to the Montreal Protocol concerning mitigating global warming impacts and accelerating the phaseout of hydrochlorofluorocarbons (HCFCs) for developed and developing countries.Amends the Clean Air Act to allow the production and consumption of class II substances that are used as fire suppression agents for military, commercial aviation, industrial, space, or national security applications and that reduce overall risk to human health and the environment compared to alternatives.Bans the importation of any product manufactured after January 1, 2010, that contains any class II substance that has been phased out of production and consumption for any purpose other [...]

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To require the Food and Drug Administration to establish a standard for broad-spectrum protection in sunscreen products, and for other purposes. 7/18/2007--Introduced. Skin Cancer Prevention, Education, and Consumer Right-To-Know Act - Amends the Federal Food, Drug, and Cosmetic Act to deem a drug that is a sunscreen product whose labeling violates this Act to be adulterated.Prohibits the labeling of a drug that is a sunscreen product that fails to meet the standards adopted under this Act from: (1) describing the product using the term "broad-spectrum"; or (2) including a specified symbol adopted to indicate broad-spectrum.Requires the Secretary of Health and Human Services to adopt: (1) a standard for broad-spectrum protection in sunscreen products; and (2) an easily recognized symbol for inclusion in the labeling of sunscreen products meeting such standards.Sets forth minimum standards that the Secretary shall adopt for such broad-spectrum [...]

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A bill to require the Food and Drug Administration to conduct consumer testing to determine the appropriateness of the current labeling requirements for indoor tanning devices and determine whether such requirements provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the skin, including skin cancer, and for other purposes. 2/16/2007--Introduced. Tanning Accountability and Notification Act of 2007 - Requires the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, to determine whether: (1) the labeling requirements for indoor tanning devices provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the eyes and skin, including skin cancer; (2) adding the warning suggested by the American Academy of Dermatology or any other additional warning to the current warning [...]

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To require the Food and Drug Administration to conduct consumer testing to determine the appropriateness of the current labeling requirements for indoor tanning devices and determine whether such requirements provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the skin, including skin cancer, and for other purposes. 2/8/2007--Introduced. Tanning Accountability and Notification Act of 2007 - Requires the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, to determine whether: (1) the labeling requirements for indoor tanning devices provide sufficient information to consumers regarding the risks that the use of such devices pose for the development of irreversible damage to the eyes and skin, including skin cancer; (2) adding the warning suggested by the American Academy of Dermatology or any other additional warning to the current warning label [...]

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