New FDA portal features and reminders aim to help facilities meet MoCRA registration renewal deadlines.
What did the FDA announce about cosmetic facility registration in February 2026?
On February 11, 2026, the U.S. Food and Drug Administration (FDA) announced updates to its Cosmetics Direct electronic submission portal and supporting materials to help cosmetic product facilities prepare for their required biennial registration renewal under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA).
The updates include:
- A dashboard displaying facility registration status and renewal dates
- Automated renewal reminders sent to registered facilities
- Updated instructions, user guides, and tutorials for submitting registrations and renewals
These enhancements are intended to improve compliance visibility and reduce the risk of missed deadlines.
What is MoCRA and who must register with the FDA?
The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) created new regulatory requirements for cosmetic manufacturers and processors, including:
- Facility registration with the FDA
- Cosmetic product listing requirements
- Safety substantiation obligations
- Adverse event reporting
- Biennial renewal of facility registrations
MoCRA applies to:
- U.S. cosmetic manufacturers and processors
- Foreign cosmetic facilities that manufacture or process products imported into the United States
When do cosmetic facility registrations need to be renewed?
MoCRA requires cosmetic facilities to renew their FDA registration every two years.
Companies that registered during the initial MoCRA implementation period should now begin preparing for their first renewal cycle.
Missing a renewal deadline could create compliance risks that may affect import operations.
How do the new FDA portal updates help companies comply?
The updated Cosmetics Direct system introduces several practical improvements:
- Real-time visibility into facility registration status
- Clear identification of upcoming renewal deadlines
- Automated reminders to prevent missed submissions
- Improved instructions and tutorials for users
These features are designed to reduce administrative burden and improve compliance accuracy for industry stakeholders.
Does this affect cosmetic importers and foreign manufacturers?
Yes. Importers should pay close attention.
If a foreign manufacturer or processor supplying products to the U.S. market fails to maintain a valid FDA registration:
- Shipments may face regulatory scrutiny
- Entry delays or holds could occur
- Compliance liability may extend to the importer
Importers should confirm that all overseas cosmetic suppliers:
- Are properly registered with FDA
- Understand renewal deadlines
- Maintain accurate facility information
What should cosmetic companies do now to prepare for renewal?
Companies should consider taking the following steps:
- Confirm current facility registration status in Cosmetics Direct
- Verify renewal dates and responsible personnel
- Review FDA guidance materials and updated tutorials
- Coordinate with regulatory and supply chain partners
- Maintain documentation supporting compliance
Early preparation can help avoid disruptions once renewal deadlines approach.
How Alba Can Help
For companies importing cosmetics or working with international manufacturers, regulatory alignment is critical.
Alba’s compliance specialists can assist with:
- Supplier verification and due diligence
- Import compliance strategy
- Regulatory risk assessments
- Supply chain coordination
If you have questions about how MoCRA requirements may impact your imports, Ask Alba™.
