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Section: Regulations > Safety

With an increase in sustainability, consumer focus and particularities from consumers about health concerns, the press release from PASS furthers the discussion of regulations in sunscreen and other application products.

PASS Weighs in on NAS Report Finding Insufficient Data for Sunscreen Bans

Responding to increased interest in sustainability and consumer health concerns, the Public Access to SunScreens (PASS) Coalition released a statement responding to recent NAS findings and furthering the discussion of regulations in sunscreens.

The company announced in 2020 that it would stop selling the baby powder in the United States and Canada.

Report: J&J Ending Sales of Talc-based Baby Powder in 2023

Reuters reports that J&J faces about 38,000 lawsuits from consumers claiming the products caused cancer due to contamination with asbestos. J&J continues to deny the allegations.

'...There is currently insufficient relevant and reliable scientific data to conduct realistic ERAs and there is not enough scientific data to support sunscreen ingredient bans,' wrote the Personal Care Products Council (PCPC).

PCPC on NAS Report: 'Not Enough Data to Ban Sunscreens'

The Personal Care Products Council has released a statement responding to the National Academy of Sciences Report, "Review of Fate, Exposure, and Effects of Sunscreens in Aquatic Environments and Implications for Sunscreen Usage and Human Health."

Revisions include adding “special cosmetics” and “cosmetics using new ingredients” to the key categories of sampling testing.

China Revises Cosmetic Sampling Testing Rules, Calls for Comments

The measures will focus on testing in children’s cosmetics, special cosmetics and cosmetics containing new ingredients. Measures are open to public comment through July 14, 2022.

Patient applying psoriasis relief cream

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.

'I’m glad we were able to work in this legislation to ensure the FDA can, at long last, provide meaningful oversight to cosmetics and dietary supplements.'

US Senate Bill to Strengthen Cosmetic Oversight Advances

Among other changes, the bill would make the FDA's Voluntary Cosmetic Registration Program mandatory.

The UK and EU have made robust regulatory changes due to recently trending ingredient concerns. Updated guidances for lilial, DHA and cyclic silicones are outlined here, along with other regional updates.

European Regulatory Update: UK and EU Ingredient Management

The UK and EU have made robust regulatory changes due to recently trending ingredient concerns. Updated guidances for lilial, DHA and cyclic silicones are outlined here, along with other regional updates.

Henkel is conducting this voluntary recall with the knowledge of the U.S. Food and Drug Administration.

Henkel Recalls Alterna Bond Repair Leave-in Heat Protection Spray

Henkel has so far received no reports of harm or injury in connection with this product.

The company responded stating its entire sun-care range is free of the two ingredients that are harmful toward reefs: oxybenzone and octinoxate.

Bondi Sands 'Reef Friendly' Sunscreen Hit with Class Action Suit

The class action suit in the United States alleges the company's sunscreens claim to be "reef friendly" while they are harmful to the environment.

As the first quarter of 2022 came to a close, several regulatory changes were announced in the Asia-Pacific region. Following is an overview, which includes ingredient restrictions, claims guidelines, adverse reactions and more.

Asia-Pacific Regulatory Update: GMPs, Safety, Ingredient Restrictions, Claims and More

As the first quarter of 2022 came to a close, several regulatory changes were announced in the Asia-Pacific region. Following is an overview, which includes ingredient restrictions, claims guidelines, adverse reactions and more.

The FDA has received reports of serious side effects including skin rashes, facial swelling and discoloration from the use of skin brighteners containing hydroquinone.

FDA Flags 12 Companies for Illicit Hydroquinone-containing Skin Brighteners

The products contain the active drug hydroquinone, rendering them unapproved over-the-counter (OTC) drugs rather than cosmetics.

China's National Institutes for Food and Drug Control (NIFDC) plans to introduce a more systematic and comprehensive standard consistent with the current industry situation.

China Drafts 2022 Safety and Technical Standard for Cosmetics

This draft will supersede the 2015 edition, which includes the overarching technical standards for cosmetics safety supervision and testing in China. Public comments will be accepted through April 30, 2022.

The plaintiffs claim the product is a misbranded drug that can cause serious side effects due to its isopropyl cloprostenate content. (Note: Depiction only; not the actual product).

Rodan + Fields to Pay Out $38 M in Lash Boost Settlement

Rodan + Fields will pay $38 million to settle several class action suits against its Lash Boost serum. The plaintiffs claim the product's labeling misleads consumers and its isopropyl cloprostenate content makes it subject to FDA oversight.

The CTPA and the U.K. cosmetic industry wants to promote the use of new approach methodologies (NAMs) as alternatives to animal testing for these vital safety requirements under other chemicals legislation, especially UK Reach.

CTPA Convenes to Progress the Use and Regulatory Acceptance of Animal Testing Alternatives

The CTPA and the U.K. cosmetic industry wants to promote the use of new approach methodologies (NAMs) as alternatives to animal testing for these vital safety requirements under other chemicals legislation, especially UK Reach.

The bacterium typically poses little medical risk to healthy individuals but could affect those with health issues such as weakened immune systems.

Kao USA Recalls Jergens Ultra Healing Moisturizer Over Microbe Concerns

Kao USA has issued a voluntary recall of specific lots of its Jergens brand Ultra Healing Moisturizer over the possible presence of Pluralibacter gergoviae.

Forty-seven percent of the products tested reportedly contained more than the permitted level of mercury.

ZMWG Reports Mercury Findings in Skin Care, Raises Public Alarm

The Zero Mercury Working Group (ZMWG), comprising 110+ global public interest and NGO health organizations, recently published findings that 129 of some 271 skin brightening products it tested contain high levels of mercury. This has raised public alarm.

Health Canada has issued recalls for three personal care products since January 2022, two for microbial contamination, and the third for potential benzene.

Health Canada Recalls Bioderma Micellar Water, Brut Deo, Equate Oral Rinse

In recent months, Health Canada has recalled Bioderma Sensibio H2O Micellar Water and Equate Dry Mouth Oral Rinse due to microbial contamination. Also, Unilever's Brut Classic Aerosol Spray deodorant was recalled for potential benzene content.

The inner packaging of a serum and product kit containing said serum listed SPF when the product has no SPF.

FDA Flags Color Additive, SPF and Contaminant Offenses, Urges 'Recall Readiness'

In recent months, the U.S. Food and Drug Administration (FDA) reported six voluntary recalls for an impermissible color additive, mislabeled SPF and several contaminants. It also urged companies to be "recall ready" and provided final guidance to do so.

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