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Registrar

Assistance with U.S. FDA Regulations

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Cosmetics

Cosmetics


Register with the U.S. Food and Drug Administration

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Cosmetics companies have a legal responsibility to ensure the safety of their products. Adherence to Good Manufacturing Practice (GMP) helps reduce the risk that a cosmetic product will be misbranded or adulterated. Registrar Corp’s Cosmetri is a software solution that empowers cosmetic and personal care businesses by streamlining operations, accelerating product development and maintaining compliance with industry regulations and GMP.

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Cosmetri by Registrar Corp

Labeling and
Ingredient Review

Labeling errors are one of the leading causes of FDA detentions. Registrar Corp helps companies modify their cosmetic labeling to comply with FDA regulations. Registrar Corp provides revised graphic files ready to be printed or edited, and a report that details the regulations, compliance guides, warning letters, import alerts, and other guidance documents from FDA.

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Certain cosmetic companies intending to sell in the state of California, USA are required to report ingredients in their products that may cause cancer, birth defects, or other reproductive harm. Registrar Corp helps companies determine which ingredients in their products may be subject to this requirement and reports them to California.

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California Safe
Cosmetics Act Reporting

MoCRA Requirements for Cosmetics 

Under the Modernization of Cosmetics Regulations Act of 2022 (MoCRA), cosmetics companies must comply with new regulations, including mandatory facility registration, product listing, adherence to GMPs, and much more. Registrar Corp helps cosmetic companies prepare for MoCRA’s extensive requirements.  

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Color Additive
Regulations

A cosmetic color additive is any dye, pigment, or other substance that can impart color to a cosmetic product. Cosmetic color additives are regulated by FDA.

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Detention Assistance

Companies shipping products to the United States may find their shipments subject to Detention Without Physical Examination (“DWPE”) by FDA. Products subject to DWPE are held at the port of entry while FDA performs additional scrutiny, testing, and analysis. Delays from DWPE may be lengthy for businesses anxious to deliver products on schedule.

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    FDA has cancelled thousands of registrations that were not properly renewed or did not include
    an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.

    Notice: Medical Device and Drug establishments that did not renew their FDA registrations in   must re-register.


    Get Help Now

    FDA-registered facilities must renew their registrations by December 31,  

    Medical Device and Drug establishments must renew their registrations by December 31,  

    Renew Now

    Reminder

    The U.S. Food and Drug Administration (FDA) requires that all registered food, medical device, and drug facilities renew their FDA registration between October 1 and December 31,

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    Notice

    The U.S. FDA Registration Renewal period CLOSED on December 31,

    If you did not renew by the deadline, you must re-register with FDA.

    Re-register or verify that your registration was renewed for :

    Re-Register
    Verify

    Limited Time Offer

    Get 18 Months of Registration and U.S. Agent service for the price of 12 when you sign up today.

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