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Type: Article

Section: Regulations > Regional

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Sunscreen Dynamics and the ‘Reef Safe’ Dance

Protection against damaging pollution, toxins and electromagnetic waves of all lengths is at the forefront of consumers’ minds; not to mention regulators’. But what happens when a topical solution to one of these forces is at odds with another?

Net Contents of a Cosmetic: The ‘E’ Mark and Units of Measure

Recently, some European Union member states have expressed concern over the misuse of the Estimated Symbol (℮), often referred to as the “e” mark, on product labels. In addition, some regulators have argued that the International System of Units, known as the metric system, should be used on all product labels to indicate the net contents of a finished product. Both of these concerns have fueled the present column in which the author debates how product labels should indicate the net contents of a cosmetic product. In closing, he comments on the jurisdiction of the CPSC in the United States.

Net Contents of a Cosmetic: The ‘E’ Mark and Units of Measure

Recently, some European Union member states have expressed concern over the misuse of the Estimated Symbol (℮), often referred to as the “e” mark, on product labels. In addition, some regulators have argued that the International System of Units, known as the metric system, should be used on all product labels to indicate the net contents of a finished product. Both of these concerns have fueled the present column in which the author debates how product labels should indicate the net contents of a cosmetic product. In closing, he comments on the jurisdiction of the CPSC in the United States.

Cosmetic Ingredients on the EU’s Dangerous Substances List

The Cosmetics Directive 76/768/EEC was recast as Regulation (EC) No 1223/2009 on Nov. 30, 2009, and this recast will totally repeal the original legislation on July 11, 2013. While the recast still contains a Dangerous Substances List, elements of the list have changed. This column distills some 1,355 pages of regulation down to review the cosmetic ingredients listed.

Asia-Pacific Update: Indonesia Cosmetics

Indonesia is home to approximately 700 cosmetic companies in its 19 provinces. In 2007, total cosmetic production reached 372 tons, with an average 12.5% increase of production from 2003 to 2007.

Companies should review all product labels and update them to include Responsible Person contact information. They should also take stock of any noncompliant inventory and assess the practicability (and cost) of relabeling those products.

How Cosmetics Companies Can Avoid MoCRA Compliance Pitfalls and Litigation

Despite MoCRA’s efforts to clarify and standardize regulations, and even though its requirements have only been in effect for a handful of months, cosmetics companies have already started to encounter pitfalls.

Does Your PIF Comply?

Does your PIF comply? European Regulation (EC) No. 1223/2009 requires that a Product Information File (PIF) be completed and kept updated for each cosmetic product placed on the EU market. What should it contain? Find out here.

Comparatively Speaking: cGMP vs. ISO

Tony O'Lenick draws on the expertise of Joe Albanese of 3V Inc. to discuss the differences between cGMP compliance and ISO certification.

Comparatively Speaking: Cosmetic vs. Cosmeceutical vs. Drug?

The Food, Drug and Cosmetics Act (FD&C Act) defines a cosmetic by its intended use, meaning cleansing, beautifying, promoting attractiveness or altering appearance.

Comparatively Speaking: Color vs. Certified Color

To follow up on the four-part series of "Comparatively Speaking" columns on color that sourced Nick Morante, the color expert continues in this column to discuss the difference between colors and certified colors.

Six Common Criteria for Cosmetic Claims in the EU

In European Cosmetics Regulation No. 1223/2009, the European Commission (EC) has chosen to regulate cosmetic claims in addition to the existing regimes, saying that consumers should be protected from misleading claims concerning efficacy and other characteristics of cosmetic products.

Updates Encouraged for Health Canada's In-Commerce List

Suppliers that export chemicals directly into Canada or that supply ingredients for finished products that are sold in Canada and, therefore, regulated under the Food and Drugs Act (F&DA) in Canada need to ensure that these substances are nominated to the revised In-Commerce List (ICL) in Canada.

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Combing Through Sun and Pollutant Effects on Hair

Trefor A Evans, Ph.D., institute fellow at TRI Princeton and long-time C&T scientific advisor, offers his insights on the latest developments in hair science and what they mean to the cosmetic formulator.

REACH Update: ECHA Urges Companies to Organize SIEFs

In a fact sheet dated Apr. 24, 2009, the ECHA reminded REACH preregistrants that it is urgent to become involved in SIEF activities as soon as possible since deadlines for registration are extremely tight.

Challenges in Creating NPA- and WFM-compliant Natural Formulations

Where does the formulation chemist begin when facing a marketing request for a product stamped with a “natural” label claim? The first step is to identify the certifying organization or government under which the formulation is to be sold, followed by the choice of preservatives. The basic approach to composing natural products is outlined here.

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Here Comes the Sun Protection: ISO Test Methods

Our knowledge of the sun and its effects on skin has increased over the years, including the damaging effects of UVA and UVB light. Testing methods for UVA and UVB rays differ; the following is a review of the testing protocols of the European Union and United Kingdom. (Click through to the Digital Edition)

A Modernization of Cosmetics Regulation Act (MoCRA) Compliance Checklist

Your proactive work to ensure compliance will help the industry move forward, increase consumer trust and loyalty and strengthen your own business.

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European Regulatory Update: Cosmetic Ingredient Changes Coming in 2025-2026

This article looks to changes in 2025-2026 to the status of ingredients in the EU and UK. Examples include nanomaterial and UV filter bans/restrictions, limits on actives, labeling formaldehyde-releasing preservatives and allergens, ecodesign and others.

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