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FDA Rule for Broad-spectrum Labeling: Key Substrate Findings

UVA protection is part of the mandatory testing for claiming broad-spectrum sun protection. A worldwide standardization is in development with the ISO TC217, expected for UVA testing 2012. The FDA has issued a final rule following Colipa’s proposed UVA in vitro method. While this rule establishes UVA labeling and testing, inconsistencies remain. This study compares the critical wavelength in roughness and application before and after two levels of UV doses.

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FDA Warns 1,500 New Sanitizer Makers: Follow the Rules

Safety and fraudulent claims are new concerns in the hand sanitizer market. Since the U.S. Food and Drug Administration (FDA) eased restrictions, some 1,500 new hand sanitizer manufacturers have registered to help; but many are not following the FDA's policy.

The virtual public meeting will inform manufacturers of agency efforts to develop regulations to establish good manufacturing practices for cosmetics.

[updated] FDA to Outline Efforts Toward Good Manufacturing Practices

The U.S. Food and Drug Administration (FDA) will hold a virtual meeting, "Good Manufacturing Practices for Cosmetic Products Listening Session," on June 1, 2023.

FDA's CFSAN to Hold Public Meeting on Cosmetic Microbiological Safety

The US Food and Drug Administration's (FDA) Center for Food Safety and Applied Nutrition (CFSAN) will hold a public meeting in Washington, D.C., USA, on Nov. 30, 2011, on microbiological safety issues relevant to cosmetic products.

FDA Adds Cosmetic Manufacturers to Import Alert for Drug Claims

The US Food & Drug Administration's (FDA) Center for Drug Evaluation and Research (CDER) has re-issued an import alert that scrutinizes cosmetic manufacturers importing antiaging products into the United States that make drug claims.

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[video] 'Harmful' Ingredients, FDA Oversight and Diversity: News and Insights

New season = new cosmetic R&D news. This week's recap covers California's potential ingredient ban, the global state of animal testing, consumer diversity, vegan and floral ingredients, polyester waste and more.

Frequency of Use of Organic UV Filters as Reported to the FDA

The author reports on frequency of use of 17 organic UV filters in nearly 18,000 formulations voluntarily reported to the United States government as of May 2003.

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FDA Reports 646 Voluntary Cosmetic Registrations in One Month

The U.S. Food and Drug Administration reported 646 cosmetic products were voluntarily registered in August 2020.

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FDA Calls Preliminary Public Meeting for International Cosmetics Regulation

The U.S. FDA announced it will hold a public meeting in June to prepare for the broader International Cooperation on Cosmetics Regulation meeting of worldwide authorities in July.

The U.S. Food and Drug Administration reported 357 cosmetic products were voluntarily registered in December 2020. This brings the total of filed products to 17,357 since 2018.

FDA Adds 357 Voluntary Cosmetic Registrations in One Month

The U.S. Food and Drug Administration reported 357 cosmetic products were voluntarily registered in December 2020. This brings the total of filed products to 17,357 since 2018.

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When it Comes to CBD, the FDA Wants to See the Receipts

The agency held its first hearing on cannabidiol (CBD) in Silver Spring, Maryland, on Friday, May 31, 2019.

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US FDA to Assess Cosmetic Safety Through Manufacturing Survey

The survey "is part of the FDA’s ongoing effort to add to [its] understanding of the cosmetic industry and manufacturing practices" in order to ensure cosmetic safety.

'Our organizations stand ready to continue to work with you and other stakeholders on a bipartisan, comprehensive and uniform national framework for cosmetics regulation...'

Industry Stakeholders Back the FDA to Modernize Cosmetic Regulations

Recently, the Personal Care Products Council, Fragrance Creators Association, Independent Beauty Association and Consumer Healthcare Products Association declared their support for modernizing cosmetic regulations in a letter to the FDA.

Certification must be performed before the color additive is permitted for use in products marketed to U.S. consumers.

U.S. FDA Proposes Fee Increase to Certify Color Additives

If finalized, the proposed rule will implement a 10 cent per pound increase in color certification fees.

FDA Closes Negotiations with ICMAD and PCPC, Prompting Industry Response

On Mar. 6, 2014, Michael Taylor, on behalf of th The U.S. Food and Drug Administration (FDA), responded to the Proposed Draft Legislation by the Personal Care Product's Council (PCPC) and the Independent Cosmetics Manufacturers and Distributors (ICMAD), effectively finding no common ground between the three and closing the negotiation.

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[video] FDA on CBD, Microbiome and Hair Innovations: Top News

From the FDA on CBD, to microbiome skin care and more, here are this week's top headline picks, as chosen by Cosmetics & Toiletries editors.

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FDA Recalls: 24 Benzene Reports + 1 Off-taste Toothpaste Account

Since mid-April 2024, the U.S. Food and Drug Administration highlighted 24 cosmetic recalls due to benzene content and one toothpaste recall for "off-taste." Here's a rundown.

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FDA Permits Compounding, Alcohol-based Hand Sanitizer Production

The U.S. Food and Drug Administration (FDA) has issued two guidance documents to communicate its policy for the temporary manufacture of certain alcohol-based hand sanitizer products, in response to the coronavirus (COVID-19) pandemic.

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