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.

The dashboard is dedicated exclusively to reports of cosmetic product adverse events, making the data easier to search. It includes serious adverse event reports submitted by responsible persons for cosmetic products under requirements established by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA), as well as voluntary adverse event reports submitted to the FDA by healthcare professionals, consumers, salon professionals, cosmetologists and others. The FAERS dashboard contains adverse event reports for cosmetic products, such as moisturizers, shampoos, conditioners, hair dyes and tattoos.

Users can search and view reports using various search terms including the product name and adverse event term. Additionally, users can filter and sort results by different criteria, such as severity level of the adverse event, date or report type. This comprehensive search capability ensures that users can efficiently locate the specific information they need from the database.

Our Services

• The United States Agent;
• The United States FDA Cosmetic Facility Registration;
• The United States FDA Cosmetic Product Listing;
• The United States FDA OTC Drug Registration;
• The United States Color Additive Batch Certification;
• The United States Cosmetic/OTC Drug Labeling Review; and
• International Cosmetic Ingredient Name (INCI) Application.

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Further Information

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