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Type: News

Section: Regulations

Beginning Dec.1, 2023, domestically produced toothpaste must be notified with the provincial-level drug supervision and administration department in the jurisdiction of the notification applicant before being marketed and sold.

China National Medical Products Administration Updates Toothpaste Regulations

Beginning Dec.1, 2023, domestically produced toothpaste must be notified with the provincial-level drug supervision and administration department in the jurisdiction of the notification applicant before being marketed and sold.

As reported in 2022, the lawsuit follows the release of findings published in the Journal of the National Cancer Institute associating hair straightening product use with incident uterine cancer. The study did highlight the fact that Black women could be disproportionately affected, as 60% of the 33,947 total participants who reported using hair straighteners self-identified as Black women.

Hair Relaxer-Cancer Lawsuits Will Move Forward

Earlier this year, racial justice organization Color of Change urged consumers to sign a petition demanding that Target, ShopRite, Giant, Food Lion and other major retailers remove "toxic" products such as lye relaxers and hair dyes from shelves.

The FDA does not intend to enforce the requirements related to cosmetic product facility registration and cosmetic product listing for an additional six months after the December 29, 2023, deadline.

FDA Delays MoCRA Enforcement by 6 Months

The U.S. Food and Drug Administration (FDA) announced it will delay the enforcement of facility registration and product listing requirements under MoCRA for six months after the Dec. 29, 2023, deadline to give the industry "sufficient time" to submit.

While the concerns expressed over these materials are not specific to cosmetics, and only two are currently listed as cosmetic ingredients, it is worth noting the potential safety issues of these materials as well as the likelihood of the bans initiated in California to spread nationwide.

California Bans 4 Food Additives, FDA Proposes Same for BVO Emulsifier

On Oct. 7, 2023, the State of California banned four food and beverage additives reportedly linked to health issues: potassium bromate, propyl paraben, Red Dye No. 3 and brominated vegetable oil (BVO). The FDA may follow suit with BVO.

October was the deadline but it came and went without a MOCRA portal to show for it.

FDA to Industry: Review SLP Guides, Gather Data Until MOCRA Portal Launches

October was the deadline but it came and went without a MOCRA portal to show for it. As the industry waits, the FDA advised members to continue collecting data and reviewing guidance documents — including the latest one for Structured Product Labeling.

Requirements range from creating an adverse event reporting system, and maintaining current and complete safety substantiation records, to ensuring facilities are registered with the FDA and more.

[poll results] How prepared are you for MOCRA requirements?

The Modernization of Cosmetics Regulation Act (MOCRA) goes in to effect on Dec. 29, 2023, giving the U.S. Food and Drug Administration increased authority over cosmetics. Are you ready for it? We want to know - please take our 1-click poll.

According to the company, the tool can save organizations hours in time typically spent on regulatory and retailer standards review.

Cosmex AI Takes Regulatory Compliance for Cosmetics to the Next Level

Those who were wondering how artificial intelligence (AI) might take cosmetic product development to the next level now have their answer. Cosmex AI can scan 30,000+ ingredients to instantly indicate if a product complies with regulators or retailers.

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.

According to the European Environmental Bureau, this indicates the commission 'bows to chemical and farm industry pressure yet again.'

EC Delays REACH Yet Again, 'Abandoning' Chemical Reform

The European Commission's 2024 Work Program was recently rolled out with a glaring omission — REACH provisions, "backtracking on its pledges made under the 2020 Chemicals Strategy for Sustainability," per the EU Observer. This was not the first time.

The ICCS is a global initiative focused on the adoption of animal-free assessments of cosmetics and its ingredients for human health and environmental safety.

Inolex and CTPA Join ICCS, Further Promote Animal-free Testing Methods

The ICCS is a global initiative focused on the adoption of animal-free assessments of cosmetics and its ingredients for human health and environmental safety.

The three-judge appeals panel reportedly wrote that 'the lower court failed to fulfill its 'gatekeeping role' of assessing whether the plaintiffs’ experts based their testimony on sound science.'

$223 M Talc Verdict Against J&J Overturned on 'Junk Science'

According to NJBiz, in an Oct. 3 ruling, a federal appeals court overturned a $223 million jury award and ordered a new trial because the awarding jurors were allowed to hear "improper scientific testimony" linking J&J's talc-based products to cancer.

For certain 'leave-on' cosmetic products, per the new restriction, due to their low contribution to the overall emissions of microplastics, as well as the potentially large impact on the cosmetics industry, the agency's committee for socio-economic analysis considered two additional measures as appropriate alternatives to the ban.

European Commission Adopts Measures Restricting Intentional Microplastics

The measures will prohibit the sale of microplastics and of products to which microplastics have been added intentionally and that release those microplastics when used.

All updates were effective immediately upon release except the revised test methods, which are scheduled to come into force on March 1, 2024.

China Updates: Benzene Limit, 19 Test Method Revisions, Benvitimod/Tapinarof Ban

China’s National Medical Products Administration (NMPA) recently issued Notice No. 41, limiting benzene impurities in cosmetics, revising five and adding 14 test methods, and banning the tapinarof skin treatment for psoriasis.

'Eleven states and 44 countries already slammed the door shut on new animal testing for cosmetics. In fact, the U.S. is essentially the only country in the North America that hasn’t passed legislation to end it.” said Sara Amundson, president of the Humane Society Legislative Fund.

US Moves a Step Closer to Banning Cosmetics Animal Testing

“Cosmetics testing on animals is cruel, unnecessary, and outdated, and Congress should finally put a stop to it."

Nanomaterials Data Submission Request Uk Adobe Stock 616588391

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.

J&J, in the meantime, is suing four doctors who published studies linking talc-based personal care and cancer based on 'junk science,' per Reuters.

J&J's Second Talc-related Bankruptcy Attempt Denied

For a second time this year, the courts have ruled against Johnson & Johnson's (J&J's) appeal to file for bankruptcy under the subsidiary LTL Management to settle talc-related suits.

The draft guidance is intended to help ensure the safety of cosmetic products that many consumers use day-to-day. The FDA is accepting comments on the draft guidance until Sept. 7.

FDA Issues Draft Guidance for Cosmetics Company Product Registration and Submission

The draft guidance is intended to help ensure the safety of cosmetic products that many consumers use day-to-day. The FDA is accepting comments on the draft guidance until Sept. 7.

The EC's roadmap will include legislative and non-legislative actions to further reduce animal testing and aim to ultimately move to an animal-free regulatory system under chemicals legislation.

European Commission to Expedite Phasing Out of Animal Testing

Responding to the ECI, the EC provided a comprehensive overview of the EU's legislative and policy framework for animal testing and proposed creating a "roadmap" to further reduce animal testing.

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