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Registrar Corp, the world’s largest cosmetics compliance firm, created the MoCRA Wizard so you can easily determine which MoCRA requirements apply.
Answer a few short questions and in less than two minutes, you’ll find out how to meet FDA’s new cosmetic compliance standards.
Complete this form to get your results and see how MoCRA will impact your business.
Based on the information you provided, it seems that you may be exempt from MoCRA's Cosmetic Facility Registration and Cosmetic Product Listing requirements. However, if you are a manufacturer, packer, or distributor of a cosmetic product and your name appears on the cosmetic label, you are required to report Report Serious Adverse Events associated with the use of cosmetic products in the United States to FDA within 15 business days.
Additionally, MoCRA will require changes to Cosmetic Labels including disclosure of fragrance allergens to be identified by the FDA and providing a US Address or electronic contact information through which the Responsible Person (or its US Agent) can receive Adverse Event Reports. Please Contact Us for assistance with these requirements or any other US FDA regulations.
Based on the information you provided, you may be exempt from MoCRA's facility registration, product listing, and adverse event reporting requirements.
MoCRA will require changes to cosmetic labels, which include:
Our labeling specialists can assist your company to assure your product labels are compliant when they reach the U.S. market. Contact us to see how we can help you achieve MoCRA compliance the right way.
Based on the answers you provided, your company needs to complete the following to comply with the requirements of the Modernization of Cosmetics Regulation Act of 2022 (MoCRA):
*For more information on each requirement, hold your cursor over the blue 'i' icon next to each requirement.
As your Authorized Agent for FDA Cosmetic Registration and Listings, Registrar Corp will:
As your U.S. Agent for FDA communications, Registrar Corp can:
Login or return to the Novi Connect platform and complete your product listings requirement.
Existing Novi Connect users, complete your product listings in half the time by leveraging your pre-loaded SKUs.
To comply with adverse event requirements, complete Registrar Corp's simple, two-step form.
To register your facility with FDA, complete the simple, two-step form through Registrar Corp, or click below to return to the Novi Connect platform.
To comply with facility registration and U.S. Agent requirements, complete the simple, two-step form through Registrar Corp.
To comply with facility registration and adverse event requirements, complete the simple, two-step form through Registrar Corp.
Existing Novi Connect users, complete your product listings in half the time by lever aging your pre-loaded SKUs.
To comply with facility registration, U.S. Agent, and adverse event requirements, complete the simple, two-step form through Registrar Corp.
Based on the information you provided, it seems that your Facility(s) and Product(s) are not subject to FDA's New MoCRA requirements. Please Contact Us for more information regarding FDA's MoCRA requirements or any other US FDA regulations.
Based on the information you provided, we need some additional information to determine how you may need to comply with FDA's New MoCRA requirements. Please Contact Us to meet with a Regulatory Advisor.
Based on the information you provided, additional details are needed to confirm which FDA MoCRA requirements your company must comply with. Return to the Novi Connect platform and contact mocra@noviconnect.com to learn more.
Click below to return to the Novi Connect platform and complete your product listings requirment.
To comply with facility registration and/or adverse event requirements, complete the simple, two-step form through Registrar Corp.
In certain cases, companies may be exempt from MoCRA requirements based on sales revenue. Our regulatory advisors can help you determine requirements and exemptions.
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