H.R.5033 - Ban Poisonous Additives Act of 2014113th Congress (2013-2014)
|Sponsor:||Rep. Capps, Lois [D-CA-24] (Introduced 07/09/2014)|
|Committees:||House - Energy and Commerce|
|Latest Action:||House - 07/11/2014 Referred to the Subcommittee on Health. (All Actions)|
This bill has the status Introduced
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Summary: H.R.5033 — 113th Congress (2013-2014)All Information (Except Text)
Introduced in House (07/09/2014)
Ban Poisonous Additives Act of 2014 - Prohibits the distribution of a food if its container is composed, in whole or in part, of bisphenol A (BPA) or can release BPA into food.
Authorizes the Secretary of Health and Human Services (HHS) to grant one-year renewable waivers to a facility for a particular container if such facility: (1) demonstrates that it is not technologically feasible to replace BPA in the container or to use an alternative container that does not contain BPA, and (2) submits to the Secretary a plan and timeline for removing BPA from such container. Sets forth labeling requirements for a product granted a waiver.
Requires the Secretary to promote and facilitate the use of BPA replacements. Prohibits replacement of BPA with substances that: (1) are known or are likely human carcinogens; (2) have been found by the Environmental Protection Agency (EPA) to be persistent, bioaccumulative, and toxic; (3) cause reproductive or developmental toxicity; or (4) are endocrine disrupting chemicals.
Requires the Commissioner of Food and Drugs (FDA) to review substances used in food containers in order determine whether there is a reasonable certainty that no harm will result from aggregate exposure to such substance, taking into consideration potential adverse effects from low-dose exposure and the effects on vulnerable populations and populations with high exposure. Sets forth remedial actions based on the Secretary's determination.Amends the Federal Food, Drug, and Cosmetic Act to require a manufacturer or supplier of a food contact substance to notify the Secretary of the identity and intended use of any such substance prior to its introduction into interstate commerce and of its determination that: (1) no adverse health effects result from low-dose exposures to such substance; and (2) such substance has not been shown, after tests which are appropriate for the evaluation of the safety of food contact substances, to cause reproductive or developmental toxicity in humans or animals.