Quality · United States

MoCRA: US FDA cosmetic facility registration

Our Huzhou plant holds a US FDA cosmetic facility registration under MoCRA, number 3016013680. MoCRA, the Modernization of Cosmetics Regulation Act of 2022, requires every facility that makes cosmetics for the US market to register with the FDA. Registration is a listing, not an approval: the FDA does not certify cosmetic factories.

US FDA cosmetic facility registration certificate for the YFF plant

What MoCRA asks of the factory

Under MoCRA, a facility that manufactures or processes cosmetics for sale in the US must register with the FDA and keep the registration current. Our plant is registered; the number is 3016013680. The registration certificate was issued through Registrar Corp on 4 November 2025 and can be confirmed through 31 December 2026.

What MoCRA asks of the brand

The brand owner named on the label, called the responsible person, lists each product with the FDA, keeps safety substantiation, reports serious adverse events, and puts a US contact on the label. We supply the formula data and facility number needed for the product listing, and the SDS, IFRA document and allergen declaration for the safety file.

Words to use, and words to avoid

CorrectIncorrect
US FDA cosmetic facility registration under MoCRAFDA certified, FDA approved
Registered facility, number 3016013680FDA certificate of approval

Using the right words matters when your buyer's compliance team reads your pack or your website.

GMP for the US market

Separately, SGS has assessed the plant against the US FDA cosmetic GMP guidelines. That statement is a third-party assessment, not an FDA inspection, and the statement itself says so. Details are on the quality page.

Questions buyers ask

Is the plant registered with the FDA?

Yes. It holds a US FDA cosmetic facility registration under MoCRA, number 3016013680.

Does registration mean FDA approval?

No. The FDA does not approve or certify cosmetic factories. Registration means the facility is listed with the FDA as MoCRA requires.

Who lists the product with the FDA?

Product listing is the responsibility of the brand owner whose name is on the label, the responsible person under MoCRA. We supply the formula data they need and our facility registration number.

Does the label need anything new under MoCRA?

MoCRA adds requirements such as a domestic contact for adverse event reports on the label. Your US responsible person or regulatory adviser confirms the full label wording.

Last updated . Reviewed by Tang Guoqiang, OEM/ODM Sales Manager at YFF Cosmetics.

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