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Section: Regulations > Regional

The Future of Hair Dyes Under the New EU Regulation: A Discussion

The “recast” of the 1976 Cosmetics Directive was intended to make things simpler, but does it? This article reviews and comments on the EU’s regulatory position on hair dyes, as of the first half of 2013.

BASF Micronized UV Filter Added to Annex VI of EU Cosmetics Regulation

BASF's Tinosorb A2B (INCI: Tris-biphenyl Triazine) has been added to Annex VI (the positive list) of the EU Cosmetics Regulation (EC) No. 1223/2009.

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UK Seeks Data, Reports on Testing the Safety of Nanomaterials in Cosmetics

The UK's Office for Product Safety and Standards (OPSS) is calling for data and any scientific information related to assessing the safety of nanomaterials in cosmetics.

The “Period After Opening” in the Jungle of EU Product Labeling

In the EU, a newly required “Period After Opening” designation on product labels has re-focused consumer information to address both a product’s safety and its functional performance over time. This has implications for consumers and for product testers.

'REACH must not be used to circumvent the Cosmetics Regulation and render the cosmetics testing and marketing bans meaningless.'

Unilever + 484 Stakeholders Urge EU Officials: Uphold Cosmetic Animal Testing Ban

In an open letter from the industry, Unilever and some 484 additional industry stakeholders pressed European lawmakers to uphold the animal testing ban for cosmetics.

While the company stands by its science, it is ending the global sales of baby powder containing mineral starch and switching to a formula based on corn starch,

$18.8 M Payout in J&J Talc Lawsuit Could Upset Settlement Offer

The ruling could sway individuals in the tens of thousands of other cases to also pursue claims in front of a jury, pressuring the judge overseeing the settlement case.

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FCA President and CEO Testifies Against Tariffs

The Fragrance Creators Association (FCA) notes that the tariffs, while aiming to promote U.S. manufacturing, would negatively impact American business and consumers while providing no additional benefit to the U.S. economy.

REACH and In Vitro Alternatives: Phototoxicity Testing

This is the third column in a continuing discussion regarding the new REACH regulations and their impact on chemical testing. The first appeared in December 2007 and discussed dermal corrosive potential testing; the second, in February 2008, covered dermal irritancy potential testing.

2005 Preservatives Use: Frequency Report and Registration

The U.S. Food and Drug Administration (FDA) compiles frequency of use data from registrations submitted through the Voluntary Cosmetic Registration Program (VCRP). Here, a review of the latest preservative data collected is presented as well as a discussion of the importance of the registration program.

Lead, Aluminum and Parabens: Myths in Cosmetics

Cosmetic companies comply with strict ingredient regulations and stay abreast of the latest scientific studies to ensure that their products are safe and efficacious. Yet, rumors still abound about cosmetic companies intentionally including toxic chemicals. This column looks into those myths, separating fact from fiction.

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ICMAD and PBA Support the Safe Cosmetics Modernization Act

Both organizations cited “enhanced consumer protection for cosmetics through stronger procedures and reporting requirements” as the reasoning behind their support.

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Momentive and Azelis Partner for Personal Care Down Under

“With [Azelis’] strong, technically-driven sales model we are confident we will further grow business together and deliver many innovative solutions answering to today’s and tomorrow’s market trends.”

Asia-Pacific Update: Hong Kong Regulations and ‘Green’ Awareness

In Hong Kong, cosmetic safety assurance is viewed as being part of the product manufacturing process, and reasonable safety will result from all the necessary production processes being followed. This update is a short review of the rules for manufacturing and selling cosmetic products in Hong Kong.

The FDA reminded consumers to check its blacklist of hand sanitizers they should not use due to methanol content, insufficient active ingredient or false and misleading/unproven claims.

FDA on Hand Sanitizers, Topical Irritation Testing and Biosimilars

Recent FDA activities include education for consumers on hand sanitizers and biosimilars, and guidance for testing the irritation/sensitization potential of topicals in relation to abbreviated new drug applications. Following is a roundup.

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New Age of Sustainable Sunscreens: Formulating for Modern Sun Care Trends

Sunscreen developers are faced with fast-moving trends, environmental considerations and regulatory hurdles. This column describes ingredients and methods to create environmentally friendly products while addressing key skin concerns.

Regulatory Review: Regulations in Chemicals, Sunscreen Labeling and Nanotechnology

There have been several changes in regulations that will impact global formulations. The most important one concerns chemicals in the European Union (EU). In addition, steps towards evaluating the safety of nanomaterials have been made by US regulatory bodies.

Regulatory Review: European Union and US OTC Drug Updates

The European Union (EU) issued the latest Adaptations to Technical Progress (ATP) on April 17, 2007. This ATP prohibited several ingredients and severely restricted an important preservative.

Canadian Environmental Protection Act and Its Personal Care Implications

Canadian Environmental Protection Act and its personal care implications.

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