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Section: Regulations > Regional

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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.

Not everyone in this photo should be using anti-aging skin care.

Gen Alpha Anti-aging Skin Care Ban Under Consideration in California

California's legislature is seeking to "prohibit the sale or delivery to a person under 13 years of age of an over-the-counter skin care product or cosmetic product advertised to address skin aging..."

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Asia-Pacific Regulatory Update: Toothpaste, TEA, Ingredient Amendments, Labeling, Vietnam’s Overhaul, PFAS and More

This article explores new cosmetic ingredient identifications and adjustments in the Asia-Pacific regions. China, Taiwan, South Korea, Indonesia, Malaysia, Vietnam and New Zealand regulatory changes throughout 2023 and into 2024 are discussed.

The session will cover topics such as INCI, GMPs, MoCRA, product safety and more.

PCPC to Unravel Misinformation, MoCRA, Claims Testing and More at NYSCC Suppliers' Day

During NY SCC Suppliers' Day, to be held May 1-2, 2024, at the Javits Center in NY, the Personal Care Products Council (PCPC) will host a separately ticketed session on cosmetic regulation on May 2. Topics will include INCI, GMPs, MoCRA, safety and more.

Cyclic silicones and microplastics face bans under REACH but both contribute to the aesthetics and performance of color cosmetics.

How Cyclic Silicone and Microplastic Bans Impact Color Cosmetic Formulating

Cyclic silicones and microplastics face bans under REACH but both contribute to the aesthetics and performance of color cosmetics. This article describes these bans and what replacing them means for color cosmetic formulating.

Notable changes in the Asia-Pacific region include adjustments to cosmetic ingredient technical standard and cosmetic pre-market management.

Asia-Pacific Regulatory Update: Children’s Cosmetics, Toothpaste, Personalized Products, Ingredients, E-commerce and More

Notable changes in the Asia-Pacific region include adjustments to cosmetic ingredient technical standards and cosmetic pre-market management.

'The most polluting industries, pharmaceuticals and cosmetics, will be required to pay at least [80%] of the cost for micropollutant removal...'

Europe's Wastewater Measure to Apply 'Polluter Pays' Fee for Microplastics, PFAS

The directive will require the removal of more nutrients and micropollutants from urban wastewater, particularly those from "toxic pharmaceuticals and cosmetics."

PFAS have been used in cosmetics such as nail polish, shaving cream, foundation, lipstick and mascara to make products more durable, spreadable or water-resistant.

New Zealand to Ban PFAS 'Forever Chemicals' from Cosmetics

As a part of several updates made to the Cosmetic Products Group Standard, the New Zealand Environmental Protection Agency announced the decision to ban PFAS on Jan. 30, 2024; the ban will go into effect on Dec. 31, 2026.

The #mydentity Guy Tang Reflect line of liquid demi permanent hair dyes is being recalled for potential contamination with nitrosamines.

Correction: Hair Products Recalled, Grande Cosmetics Settles and Sephora/Target 'Clean' Beauty Suits Continue

This roundup of products in "hot water" includes recalls on a hair dye and shampoo, Grande Cosmetics' settlement and a look at the latest "clean" beauty suits against Sephora and Target.

Xforms is just one digital option available for creating an SPL file with cosmetic product facility registration and product listing information. Two additional electronic options are available.

FDA Debuts Digital SPL Xforms, Paper Forms for Cosmetics Facility, Product Submissions

The FDA has rolled out Structured Product Labeling (SPL) Xforms, a digital tool, and downloadable PDF forms to register cosmetic product facilities and list products, as mandated by MoCRA.

“We are excited to welcome Emily back to lead our legal team and guide our industry’s legal and regulatory strategies,” said Tom Myers, PCPC’s president and CEO. “Her diverse and extensive expertise will be instrumental in navigating our industry’s complex legal and regulatory landscape, enhancing our support to member companies.”

The Personal Care Products Council Names VP Legal and Regulatory Affairs and General Counsel

Manoso previously worked as PCPC’s associate general counsel and staff counsel and has served as a trail attorney for the U.S. Department of Justice.

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FDA Opens Cosmetics Direct Registration Portal for MoCRA

Cosmetics Direct is an FDA Structured Product Labeling authoring tool that, according to the FDA, features user-friendly data entry forms.

A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.

FDA Releases Update to Ongoing Activities Related to Serious Adverse Event Reporting for MoCRA

A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.

According to the European Commission's Safety Gate, numerous products, ranging from soaps and fragrances, to body care, shampoo, bath milk and others, have been flagged for the present of the fragrance allergen butylphenyl methylpropional.

Recall Alert: L'Oreal's Mizani, J&J's Clean & Clear, Marcelle's 40+ Cream and Others

Globally, within the past couple of months, numerous cosmetic product recalls have been issued for microbe contamination and fragrance allergens, among other contaminants. Following is a roundup.

'I think the biggest game-changer about [MoCRA's] ... requirement for GMPs is how it changes what it means to be adulterated,' Brandi Reinbold, senior manager of global certification for NSF International, said in this sponsored videocast. Register now to watch and learn more. It's free.

[video] GMP Standards to Meet MOCRA and Retailer Mandates of the Future

While the enforcement of MoCRA has been delayed until July 1, 2024, this is no time to rest on our laurels. As this sponsored video from NSF International explains, there's much to do and it will take time. Register now to watch and learn how to prepare.

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.

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.

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