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Section: Regulations

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Laying Down the Law: EU Labeling Requirements

Consumer information is an important part of the European Cosmetics Regulation and consists of two major components: product labeling and claims. This installment lays down the labeling laws.

Comparatively Speaking: Cosmetic Labeling in the United States

In this excerpt, Tony O'Lenick looks to Perry Romanowski to explain how to list ingredients on a cosmetic product label in the United States, for the benefit of novice formulators.

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VIDEO: Is there a Future for Hand Sanitizers?

In this third video in a series, David C. Steinberg predicts the outlook for future consumer hand sanitizers in light of the FDA's triclosan ruling.

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Animal Testing's in the Hot Seat in Korea

Activists for alternatives to animal testing and industry groups hosted a forum to pressure Korea's lawmakers to prioritize investment in new approaches to cosmetics safety testing.

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FDA Sets Regulatory Framework for Regenerative Biological Therapies

It's a sign of the times when technology and innovation hit a point where the U.S. Food and Drug Administration must stop and write new rules to ensure consumer safety. That time, with respect to regenerative biological therapies, is now.

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Tox Testing at the Speed of Light (Really)

Until now, testing chemicals for their toxicity has relied on reporter genes, which can take 24 hr to deliver results. A new approach from North Carolina State University, however, uses a modified protein that emits light when binding occurs—effectively signaling its safety.

If you have registered under the Voluntary Cosmetic Registration Program (VCRP), you may be covered for the initial registration. However, cosmetic product registrations must be updated annually. New products must be registered within 120 days of introduction into interstate commerce.

7 Implications of the Modernization Act for Cosmetics

President Biden signed HR 2617 into law. What does this mean for cosmetic manufacturers? "A lot," according to Steinberg & Associates. The 1,653-page bill includes 14 pages on cosmetics. Read on to learn more.

ACC Defends the Safety of Confidential Products

The American Chemistry Council (ACC) has assured consumers that confidential products launched to the market are safe and notes that the confidentiality of these products protects innovation and jobs.

When Ingredient Alarm Leads to the Courtroom

The personal care industry has experienced growing consumer interest in the ingredients its products contain. This interest has resulted in better responsibility and safety among cosmetic manufacturers; however, it also has produced elevated concerns over potentially harmful ingredients.

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The Safe Cosmetics Modernization Act Gains Momentum

Support for H.R. 4075, the Safe Cosmetics Modernization Act, is gaining momentum with recent backing from two U.S. congressional leaders, including a Democratic cosponsor. ICMAD applauds the move.

Loose plastic glitter used as a cosmetic product can continue being sold until Oct. 16, 2029, for leave-on cosmetics.

How the EU Microplastics Ban Affects Glitter

The European Commission's (EC's) ban on microplastics intentionally added to cosmetics went into effect on Oct. 17, 2023. This includes some forms of glitter, individually and in mixtures, which the commission explained in a recent Q&A.

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Will the U.S. Finally Ban Animal Testing for Cosmetics?

It's been attempted before, so will U.S. legislators succeed this time in a nationwide ban against animal testing for cosmetics? The U.S. Humane Society believes so; and it appears the industry is on board.

Europe Harmonizes Organic Cosmetic Regulation with the COSMOS Standard

Europe has harmonized organic personal care standards with the launch of the European Cosmetics Standards Working Group's Cosmetics Organic Standard.

EU Regulatory Update: Recast of the Cosmetics Directive Published

Regulation (EC) No 1223/2009 was published on Dec. 22, 2009 with the intent to simplify rules and procedures related to the marketing of cosmetic products, a need resulting from different implementations of the Cosmetics Directive.

Establishing the Dividing Line: Is Your Product a Drug?

To avoid regulatory penalties, a company developing an OTC product must institute properly administered shelf-life testing programs as an integral part of its product development and marketing efforts.

'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.

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Regulating Risk: Fragrance Safety for the 21st Century

Clear-cut guidance has been given to establish fragrance safety based on RIFM’s scientific assessment and IFRA’s standards. This article elucidates the work of the fragrance industry to mitigate sensitization and assure the safety of its products.

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Symrise Supports the Amazon with Biodiversity and Sustainability

Symrise is a supporter of biodiversity in the Amazon region and has developed a project to improve the value chain for farmers and cooperatives, in addition to researching materials from the area for fragrance and personal care products.

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