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FDA Launches Real-Time Adverse Event Reporting Dashboard for Cosmetic Products | Customs & International Trade Law Blog

FDA Launches Real-Time Adverse Event Reporting Dashboard for Cosmetic Products | Customs & International Trade Law Blog


On September 12, 2025, the U.S. Meals and Drug Administration (FDA) introduced the launch of the FDA Adversarial Occasion Reporting System (FAERS) Public Dashboard for Beauty Merchandise. The system is an interactive software designed to facilitate the general public’s capability to look and discover real-time antagonistic occasion knowledge on beauty merchandise. By way of the software, customers can search and look at studies utilizing search phrases, together with the product identify. Customers can even obtain knowledge units and report listings. The FDA will replace the software every day to make sure it consists of the latest submissions.

The dashboard consists of critical antagonistic occasion studies submitted by accountable individuals for beauty merchandise underneath necessities established by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA), in addition to voluntary antagonistic occasion studies submitted to the FDA by healthcare professionals, shoppers, salon professionals, cosmetologists, and others. 

This announcement follows a latest launch of real-time reporting of antagonistic occasion and medicine errors knowledge for medication and therapeutic biologics. 

Within the announcement, the FDA said these real-time reporting instruments are a part of the company’s dedication to transparency and offering larger perception into the protection and regulation of the merchandise shoppers use every single day. Notice: Experiences on this dashboard haven’t been verified by the FDA, and their publication doesn’t point out thon the FDA has concluded the product precipitated the antagonistic occasion. 

Diaz Commerce Regulation supplies help with FDA pre-compliance in addition to help in efficiently navigating FDA enforcement actions. For help with cosmetics compliance necessities, required registration, reporting, or different FDA issues, contact us at 305-456-3830 or data@diaztradelaw.com.

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