Formaldehyde-containing hair-smoothing products are “injurious to users” and thus should be deemed adulterated under the Federal Food, Drug and Cosmetic Act, the Environmental Working Group and Women’s Voices for the Earth say in a 15 June petition asking the agency to implement a ban.
US FDA Inaction On Formaldehyde In Hair-Smoothing Products ‘Unconscionable,’ Petitioners Say
The Environmental Working Group and Women’s Voices for the Earth try again with a petition to the US Food and Drug Administration seeking a ban on use of formaldehyde and equivalents in heated hair-straightening products. This time they are joined by 75 concerned salon workers.
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Some FDA employees who were recently laid off by the Trump Administration are being called back to work, multiple sources confirmed to the Pink Sheet.
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Qnovia notes NRT inhalation product recently received investigational new drug clearance from FDA as agency and NIH say innovation needed smoking cessation to help improve rate of success for quitting the habit that kills around 500,000 US consumers annually.
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The Washington State Department of Ecology will try to work with companies that violate the Toxic Free Cosmetics Act, rather than reflexively imposing the $5,000-per-violation fine for first-time offenders, says the law’s implementation planner. She noted financial assistance is available for small businesses, as well as incentives for companies adopting measures “beyond compliance.”
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The Washington State Department of Ecology will try to work with companies that violate the Toxic Free Cosmetics Act, rather than reflexively imposing the $5,000-per-violation fine for first-time offenders, says the law’s implementation planner. She noted financial assistance is available for small businesses, as well as incentives for companies adopting measures “beyond compliance.”
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US FDA Office of New Drugs Director Peter Stein says review divisions have made the case that a discussion-only meeting would solicit the necessary input.
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Requests for “enforcement actions are not within the scope of FDA’s citizen petition procedures,” CDER says, rejecting petition dosing device firm Parenteral Technologies submitted as it prepares for workshop on Pediatric Research Equity Act requirements for OTC NDA sponsors.