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Section: Regulations > Regional

Initially designated as drugs in the U.S., sunscreens have been stifled under regulations and bureaucracy. This article reviews how it came to this, where current regulations stand and proposes a few “pipe dream” solutions.

Sunscreens and Pipe Dreams for their Regulation in the US

Initially designated as drugs in the U.S., sunscreens have been stifled under regulations and bureaucracy. This article reviews how it came to this, where current regulations stand and proposes a few “pipe dream” solutions.

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Health Canada Updates Hotlist Ingredients: Colorants, Benzophenone, Talc and More

Concerns including adverse developmental and maternal effects were cited for the four ingredients added. Five amendments also were made, updating the hotlist for the first time since 2022. This follows a recent recall over henna cones containing phenol.

Voluntary Registration of Cosmetics and 2007 Frequency of Preservative Use

This report details recent trends in preservative use based on VCRP data submitted to the FDA by manufacturers. The author encourages companies to participate in this program to build credibility for self-regulation and to protect their own business interests.

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6 Sanitizer Offenses, Color Additives and Cosmetic Registrations: FDA Update

The U.S. Food and Drug Administration recently issued updates regarding color additives certification, voluntary cosmetic registrations and hand sanitizer violations.

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Methanol Content and How to Test for it: FDA Guidance

The U.S. Food and Drug Administration has outlined a policy for companies to test alcohol (ethanol) or isopropyl alcohol for hazardous methanol content prior to their use in hand sanitizer products.

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Cosmetovigilance and Safety Assessment in the World of Active Ingredients

It can be deduced from today's scientific literature that countless ingredients have been developed with the intent to alter the structure and function of human skin. This raises important questions in terms of how these products should be regulated and what types of safety standards they should be held to.

Testing Tactics: REACH and In vitro Alternatives: Skin Irritation Testing

Welcome back to a continuing discussion regarding the new Registration, Evaluation and Authorization of Chemicals (REACH) regulation and its impact on chemical testing. It is the purpose of this series of articles to provide an overview of these existing validated in vitro methods, as well as new methods that are being considered for validation.

Testing Tactics: REACH and In vitro Alternatives: Skin Irritation Testing

Welcome back to a continuing discussion regarding the new Registration, Evaluation and Authorization of Chemicals (REACH) regulation and its impact on chemical testing. It is the purpose of this series of articles to provide an overview of these existing validated in vitro methods, as well as new methods that are being considered for validation.

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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[video] Import Violations, Personalized Plasma Skin Care and Partnerships: Editor Picks

This week's top picks from Cosmetics & Toiletries include the Greenbrier International/Dollar Tree import violation, SoME— a personalized skin care collection which incorporates plasma and new partnership with Clariant and Plant Advanced Technologies (PAT).

EU Regulation No. 1223/2009 Part 2: Prohibited Ingredients, Definitions and More

In total, EC No. 1223/2009, often called the Recast or the 8th Amendment, is comprised of a preamble with 71 parts (justification), 40 articles (replacing the old 15) and 10 annexes (replacing the old nine).

Cosmetics Registration in California and the FDA's Electronic-only Drug Registration

The stars where poorly aligned on June 15, 2009, when California finally issued its registration procedure and forms for the California Safe Cosmetics Act of 2005. At the same time, the US Food and Drug Administration (FDA) moved to an electronic-only filing system for drug registrations. These two changes have created significantly more work for the personal care industry—and with questionable benefits.

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Pick and Choose—Balancing Sunscreen Benefits: Sun Protection or Vitamin D?

It’s well-known that over-exposure to UV light is harmful to the body, yet it is vital for production of essential vitamin D. Understanding the balance between the benefits of sun protection and vitamin D synthesis is not yet well understood.

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PCPC/FDA Briefing: VOCs, CBD, PFAs, Talc and the Safe Cosmetics Act

VOCs, CBD, 1,4-dioxane, talc, transparency, PFAs, formaldehyde, allergens and the Safe Cosmetics Act are among the top current areas of focus for the PCPC and FDA. These and other topics were discussed during the PCPC's virtual summit, held May 11-13, 2021.

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.

Voluntary Registration of Cosmetics and 2007 Frequency of Preservative Use

This report details recent trends in preservative use based on VCRP data submitted to the FDA by manufacturers. The author encourages companies to participate in this program to build credibility for self-regulation and to protect their own business interests.

The U.S. Hemp Roundtable said the FDA’s comments signal 'the new year may offer some promise for the long-awaited regulation of hemp-derived extracts such as CBD.'

FDA to Explore CBD, Hemp Regulations for Food and Supplements

The U.S. Food and Drug Administration (FDA) is exploring whether legal cannabis is safe in food or supplements and expects to make recommendations in the coming months for regulating such products. Could this translate to cosmetics?

A letter from the FDA to Valisure, dated Dec. 5, 2022, highlighted 'methodological deficiencies' and 'analytic descrepancies' in the company's testing.

FDA, Unilever and GSK Challenge Valisure's Benzene Findings, Test Methods

The FDA recently raised concerns over the test methods of Valisure, the Connecticut-based lab whose reports over benzene in sunscreen and dry shampoo products from Unilever, GSK and others have prompted recalls and class action suits.

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