tags

United States
Cosmetics
Minnesota Announced Second Extension of PFAS Products Reporting Deadline to September 15, 2026

On April 15, 2026, the Minnesota Pollution Control Agency (MPCA) announced a second extension of the initial PFAS products reporting deadline, moving it from July 1, 2026 to September 15, 2026. Upon completion of the initial report, subsequent annual reports are due each February 1. Manufacturers unable to meet the deadline may apply for a single 90-day extension (to December 14, 2026).

Panoramic Analysis: Current Regulatory Status and Compliance Challenges of Exosome Cosmetics Worldwide

Globally, the regulatory landscape for exosome cosmetics exhibits significant variability. This article systematically reviews the management measures, regulations, and ethical standards concerning exosome cosmetics in various countries/regions, including the United States, the European Union, Japan, South Korea, Taiwan, and mainland China. It explores the context of compliance and prohibitions, as well as their impact on industry development, providing comprehensive global regulatory compliance guidance for cosmetic companies.

U.S. FDA Launches New Adverse Event Monitoring System

On March 11, 2026, the U.S. Food and Drug Administration (FDA) launched a new unified platform for analyzing adverse event reports, known as the FDA Adverse Event Monitoring System (AEMS). This initiative marks a significant milestone in the agency’s mission to modernize and enhance transparency regarding the safety of regulated products.On March 11, 2026, the U.S. Food and Drug Administration (FDA) launched a new unified platform for analyzing adverse event reports, known as the FDA Adverse Event Monitoring System (AEMS). This initiative marks a significant milestone in the agency’s mission to modernize and enhance transparency regarding the safety of regulated products.

Regulatory Trends and Compliance Strategies for PFAS in Cosmetics

Per- and polyfluoroalkyl substances (PFAS) are increasingly becoming a focal point of global concern due to their potential long-term impacts on the environment and human health. As a class of synthetic chemicals characterized by high stability and widespread applications, PFAS are facing increasingly stringent regulatory scrutiny in the cosmetics sector. This article explores the physicochemical properties and potential health risks of PFAS, and systematically reviews the evolving global regulatory landscape related to their use in cosmetics. It aims to help cosmetic enterprises gain a comprehensive understanding of regulatory requirements, mitigate compliance risks, enhance product safety, and strengthen competitiveness in international markets.

US FDA Launches Real-Time Adverse Event Reporting Dashboard for Cosmetic Products

On September 12, 2025, the U.S. Food and Drug Administration (FDA) announced the launch of the FDA Adverse Event Reporting System (FAERS) Public Dashboard for Cosmetic Products, an interactive tool designed to facilitate the public’s ability to query real-time adverse event data on cosmetic products. The user-friendly platform allows users to download report listings or data sets, with reports being updated daily to include the most recent submissions.

United States Notifies New Regulation Restricting Formaldehyde in Cosmetics, Effective September 28, 2025

This regulation restricts the manufacture, sale, and distribution of cosmetic products in the state of Washington that contain intentionally added formaldehyde or formaldehyde releasers. The objective is to reduce consumer exposure to formaldehyde through the use of cosmetic products, due to its known health risks. The regulation will enter into force on September 28, 2025.

Regulatory Updates on Global Cosmetics-Europe & Americas Overview (First Half of 2025)

This article reviews and summarizes the latest international cosmetic regulatory developments in the first half of 2025, with a focus on the European and American markets. It covers key updates from the EU, the UK, the US, Canada, and other relevant countries and regions. The aim is to help enterprises stay informed of regulatory changes, ensure compliant product launches, and enhance global market competitiveness.