September 2024 Cosmeservice Newsletter
Navigating the realm of cosmetic regulations? We have the most recent industry updates. Let's set out on this journey together!
Fragrance allergens at cosmetic products: The MoCRA update and more
As highlighted in our recent webinar, the United States is still pending the release of the draft regulation on fragrance allergens required by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). The FDA has yet to establish a definitive timeline for these regulations, including the mandatory disclosure of fragrance allergens in cosmetic labeling.
Meanwhile, California has moved ahead, requiring disclosure of any EU-listed fragrance allergens from January 1, 2024, under The Cosmetic Fragrance and Flavor Ingredient Right to Know Act—though this information will only be available online, affecting consumer access.
In response to similar EU directives, Canada now mandates that the initial 24 fragrance allergens be listed on product labels when concentrations exceed specified limits. This requirement will expand after August 1, 2026, to include all allergens, with full compliance required by August 1, 2028.
Cosmetovigilance: Secure your cosmetics once on the market.
Cosmetovigilance is a crucial system in the cosmetic industry, focusing on the rigorous monitoring of product safety after they reach the market. This system is vital for the early detection and management of any adverse effects that could arise from cosmetic use. It operates through the thorough collection, evaluation, and interpretation of safety data, ensuring that any potential risks to consumers are quickly addressed.
The core aim of cosmetovigilance is to boost consumer protection by continuously assessing the safety profiles of cosmetics throughout their market lifecycle. This includes a detailed analysis of incident reports, consumer feedback, and scientific research to identify any safety concerns.
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The enforcement of cosmetovigilance protocols mandates companies to undertake necessary corrective actions, such as product reformulation, issuing safety alerts, or product recalls. Such measures not only protect public health but also enhance consumer trust in cosmetic products.
PIF, All You Need to Know!
The Product Information File (PIF) is a crucial document in the cosmetics industry, serving as a comprehensive record that validates the safety, efficacy, and regulatory compliance of cosmetic products. This extensive collection of data goes beyond mere bureaucracy; it is foundational to ensuring consumer safety and maintaining product integrity.
The PIF is meticulously assembled with precise information, covering the qualitative and quantitative makeup of the cosmetic product, its physical, chemical, and microbiological characteristics, efficacy details, and a thorough safety assessment. This assessment, a critical element of the PIF, is performed by a certified safety assessor and scrutinizes the toxicological profiles, chemical structures, and consumer exposure levels of ingredients.
The process of creating and updating the PIF is dynamic, adapting to changes in product development, scientific advances, and regulatory modifications. It is imperative that the PIF be maintained in a readily accessible format as specified by regulatory authorities, particularly within the European Union, and updated continually to reflect any alterations in product formulation or regulatory requirements.
Don't forget to visit our blog to keep up with the latest cosmetic regulatory news!