Mocra

The Modernization of the Cosmetics Regulation Act 2022

MoCRA Product Listing

MoCRA Resource Navigation

Upate to US MoCRA

US FDA announces enforcement discretion delay until July 2024 for Product Listing and Facility Registration

9th November 2023

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Latest MoCRA Guidance

A full and practical guide on understanding MoCRA
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MoCRA Timeline

A summary of key dates to include in your MoCRA Plan
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MoCRA Support Services for Brand Owners

Services for Brands that require MoCRA support
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MoCRA Support Services for Manufacturers, Packers and Fillers

Information and services for Manufacturers, Packers and Fillers that require MoCRA support
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MoCRA Training

Learn more about Delphic HSE MoCRA webinars and other training options
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Safety Substantiation for the US under MoCRA

MoCRA requires that the RP ensures, and maintains records to support, the safety of each Cosmetic Product
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MoCRA Product Listing

MoCRA requires for the RP to submit a ‘Listing’ for each Cosmetic Product
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Ask an Expert

If you require any further assistance, please contact our team of MoCRA experts
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Frequently Asked Questions about MoCRA

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Non-MoCRA Support

To learn more about other Delphic HSE global services
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MoCRA requires for the Responsible Person submit a ‘Listing’ for each Cosmetic Product that is available on the market in the USA under their name. Such a Product Listing will require the following information to be submitted (Sec. 607, (c), (4)):

  • The Facility Registration Number of each Facility where the Cosmetic Product is Manufactured or Processed.
  • The name and contact number of the Responsible Person
  • Name for the Cosmetic Product, as it appears on the label
  • Applicable Cosmetic Category(ies) for the Cosmetic Product
  • List of Ingredients, including any
    1. Fragrances
    2. Flavors
    3. Colors
  • Product Listing Number, if one has been previously assigned during Listing

The deadline for Product Listing is the 29th December 2023 for every Cosmetic Product that is currently available in the USA.

Following this date, the Responsible Person must list any new Cosmetic Products that enter the USA Market within 120 days of Marketing such product. MoCRA also requires that Responsible Person’s update their Product Listings every year (Sec. 607, (c), (2)).

labelling
Safety substantiation
labelling

How can Delphic HSE help?

Delphic HSE has a dedicated global team, trained and ready to formally list the product on behalf of our clients. The formal registration, on behalf of the Responsible Person, can also be supported through our registered US Agent. Delphic HSE has now registered our office based in Nevada (Delphic HSE Solutions US).

While the registration of the Product is important, of greater importance is to ensure that the Product is safe and the pack, the data, and the documentation is compliant. In the event where Delphic HSE has NOT previously provided safety and/or compliance work on the product being listed, Delphic HSE can provide a recommended Compliance Summary. This Compliance Summary will include:

  • A summary of Product Listing and formal certificate/registration number
  • A summary of the Product data that has been provided to Delphic HSE
  • Recommendations on future actions, based on the data that we have received

IMPORTANT – Please note, the above Compliance Summary will not be a substitute for a formal product safety and compliance review. These services can be provided, by Delphic HSE, separately or in addition to the Product Listing Service. The Compliance Summary should be considered as a guide on current observations and future compliance recommendations.

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