US FDA MoCRA Cosmetic Registration | XPRO America
U.S. COSMETIC REGULATORY SUPPORT

US FDA MoCRA Cosmetic Registration Prepare your cosmetic business for applicable U.S. FDA requirements.

The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) introduced important requirements for many cosmetic businesses. XPRO America can help you understand the process and organize information for applicable cosmetic facility registration and product listing obligations.

Types of MoCRA Support

Support needs vary according to your role, products, facility activities, and applicable exemptions. Common areas to review include:

Cosmetic facility registration
Cosmetic product listing
Responsible person information
Product and ingredient details
Facility and business information review
Renewal and update planning

Why MoCRA Compliance Matters

Understand applicable obligations

Identify which registration, listing, and information requirements may apply to your business.

Keep records organized

Prepare consistent facility, responsible person, and cosmetic product information for review.

Plan for updates

Build a process for reviewing changes to facilities, responsible persons, and marketed products.

Support business readiness

Respond more confidently to compliance questions from partners, retailers, and importers.

Advantages of Guided MoCRA Assistance

Clearer Steps
A structured view of the information and tasks to review.
Organized Records
Help arranging facility and product information.
Update Planning
Make follow-up reviews and applicable updates easier to track.

Important Regulatory Note

Requirements and exemptions depend on the business, facility, product, and role involved. MoCRA registration or product listing is not FDA approval, certification, or endorsement. This page provides general information, not legal advice; confirm current requirements with FDA guidance or a qualified regulatory professional.

Frequently Asked Questions

What does MoCRA stand for?

MoCRA stands for the Modernization of Cosmetics Regulation Act of 2022, which changed aspects of the U.S. FDA's cosmetics regulatory framework.

Are facility registration and product listing the same?

No. Facility registration concerns an eligible facility, while product listing concerns cosmetic products marketed in the United States. Different requirements and exemptions may apply.

Does every cosmetic business have the same obligations?

No. Requirements depend on the business's role, activities, products, and applicable statutory exemptions.

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