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Type: News

Section: News

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Sunscreen Symposium Debates SPF, UVA/UVB, FDA Proposal and More

The Florida Chapter SCC Sunscreen Symposium kicked off with a splash as Guy Padulo, national president of the SCC, announced the event has approached 400 attendees.

FDA Director Honored

Cosmetic Ingredient Review (CIR) director and scientific coordinator Alan Andersen, Ph.D., has been awarded with the Distinguished Alumni Award...

The FDA Discusses Technology

The first public meeting on FDA-regulated products containing nanomaterials will take place on October 10, 2006.

FDA Appoints General Counsel

Gerald F. Masoudi has been appointed as associate general counsel/chief counsel of the Food and Drug Division of the United States Department of Health and Human Services' Office of the General Counsel.

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A Chance For FDA Regulatory Clarification

The Independent Cosmetic Manufacturers and Distributors (ICMAD) Association will return to southern California for the 27th edition of its FDA Cosmetic Regulations Workshop.

FDA Fellowship to Attract Scientists

A two-year fellowship program launched by the US Food and Drug Administration (FDA) is aimed at attracting scientists, engineers and health professionals to the agency to aid in decision-making.

The company’s colorants are sustainable with precision manufacturing practices, offering long shelf life while reducing any food or animal extracts.

RK Pigments Manufactures FDA Batch-certified Colorants

RK Pigments’ colorants are sustainable, processed using precision manufacturing practices and offer long shelf life while reducing any food or animal extracts.

Olumiant is a Janus kinase (JAK) inhibitor, which blocks the activity of one or more of a specific family of enzymes, interfering with the pathway that leads to inflammation, thereby, treating patients with alopecia areata.

FDA Approves First Systemic Alopecia Areata Treatment

Olumiant is a Janus kinase (JAK) inhibitor, which blocks the activity of one or more of a specific family of enzymes, interfering with the pathway that leads to inflammation to thereby treat patients with alopecia areata.

FDA Reagan-Udall Board to Accelerate Science

The FDA announced the new board members and chair for the Reagan-Udall Foundation, formed to advance cosmetic product development and innovation, and to enhance product safety, among other duties.

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FDA Alert: New J&J Baby Powder Recall

According to the FDA, a test sample from one lot was found to contain chrysotile fibers, a type of asbestos. As such, Oct. 18, 2019, Johnson & Johnson voluntarily recalled the product.

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ICMAD to Host FDA Cosmetics Regulations Workshop

The meeting will include a mixture of presentations and panel discussion on topics related to manufacturers and marketers of cosmetics and over-the-counter (OTC) drugs, such as I.S. FDA activities and changes in OTC drug regulations

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[update] FDA April Meeting for June ICCR-14 Meeting Cancelled

In light of the COVID-19 outbreak, the FDA has cancelled the public meeting originally scheduled for April 14, 2020, to discuss topics for the international ICCR-14 meeting on cosmetics regulation, still planned (thus far) to be held from June 8 to June 10, 2020.

'The FDA has stopped accepting and processing submissions to the VCRP as a result of [the] FDA’s plans to develop a program for submission of the facility registrations and product listings mandated by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA).'

U.S. FDA Shuts Down Voluntary Cosmetic Registration Program

In an unexpected move, the U.S. Food and Drug Administration (FDA) has shuttered the Voluntary Cosmetic Registration Program (VCRP) and underscored this data will not migrate to the MOCRA portal.

'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.

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.

A letter from the FDA to Valisure, dated Dec. 5, 2022, highlighted 'methodological deficiencies' and 'analytic descrepancies' in the company's testing.

FDA, Unilever and GSK Challenge Valisure's Benzene Findings, Test Methods

The FDA recently raised concerns over the test methods of Valisure, the Connecticut-based lab whose reports over benzene in sunscreen and dry shampoo products from Unilever, GSK and others have prompted recalls and class action suits.

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FDA Approves Dermavant’s VTAMA Cream, 1%, for the Treatment of Plaque Psoriasis in Adults

Approved for mild, moderate and severe psoriasis with no restrictions on duration of use or body surface, see why VTAMA Cream, 1%, may help your patients.

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Clariant First Half 2016 Sales Released

Clariant significantly improved their operating cash flow and have a higher profitability for the first half of the year.

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