Triclosan: Regulation and PolicyEPA publishes petition to ban Triclosan for public comment (December
8, 2010) EPA announced a 60-day public comment period for the petition
filed by Beyond Pesticides and Food and Water Watch to ban the controversial
antimicrobial pesticide Triclosan for non-medical use. The petition filed
on January 14, 2010 identified pervasive and widespread use of Triclosan
and the agency's failure to address Triclosan's impacts on human and environmental
health, conduct assessments for residues in drinking water and food and
concerns related to antibacterial resistance and endocrine disruption.
The petition cites various violations of numerous environmental statues
including the Clean Water Act, Safe Drinking Water Act and the Endangered
Species Act. Congresswoman
Urges FDA to Ban Triclosan. Beyond
Pesticides tells FDA that Triclosan is too hazardous to the aquatic environment
Groups tell EPA to restrict Triclosan (December 29, 2008). Groups sign statement seeking to restrict Triclosan citing EPA health and environmental standards too weak (read comments to EPA). Tell EPA to ban the non-medical uses of Triclosan. EPA releases
Triclosan RED, allows continued use of toxic chemical (October
29, 2008). The EPA released its final Reregistration Eligibility Decision
(RED) document for Triclosan which contained several amendments to the
risk assessment as a result of comments submitted by Beyond Pesticides
dozens of public health and environmental groups. However, despite many
lingering issues related to Triclosan's continued threat to human and
environmental health, the agency concluded that Triclosan is eligible
for reregistration. Groups Tell EPA to Stop Uses of Anti-Bacterial Consumer Products (July 7, 2008). In comments to EPA on its new risk assessment and evaluation of the widely used anti-bacterial chemical Triclosan groups point to health and environmental effects and call for end to consumer products. Read the press release and comments to EPA. FDA asks for data on Triclosan (October, 25, 2005) The Non-Prescription Drug Advisory Committee of the U.S. Food and Drug Administration (FDA) issued a call for further research regarding the risks and benefits of specific consumer antibacterial products.
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you know…? The U.S. EPA and the FDA share responsibility for regulating antimicrobial products. If an antimicrobial product is intended for use on the human body, it falls under the jurisdiction of FDA, rather than EPA. FDA categorizes Triclosan and other antimicrobial products based on use and product claims. If a product makes a health related claim, such as “kills germs” (soap, first aid creams, etc.), FDA registers it as a drug. If it makes no claim at all or if its claims are cosmetic, such as “fights odors” or “improves skin” (deodorant, makeup, shaving cream), it is registered as a cosmetic. All uses not applied to the human body (bathroom and kitchen cleaners, hospital disinfectants), that make pesticidal claims, such as “kills bacteria and mildew” are regulated by EPA as pesticides. In spite of shared responsibility, the FDA and the EPA have done little to warn consumers of the possible health and environmental effects of Triclosan. |