Holder
The named legal entity must match the company being evaluated.
Verified Manufacturing Proof
Skincare Manufacturing Certifications
Review Rixin’s cosmetic manufacturing certifications and facility registration by exact holder, location, scope, responsible body, record number, stated validity, and limitations. Each record should be matched to the entity, facility, product direction, and target-market requirements of your project.
Record review
Certification Proof Should Be Specific
A logo alone does not show whether a record applies to your project. Confirm the named legal entity, facility, scope, responsible body, record number, and validity or renewal conditions. Also distinguish third-party certification from facility registration or social audit. None of these records automatically approves a formula, product, label, claim, or market launch.
Facility
The address must match the proposed manufacturing location.
Scope
The scope must cover the relevant manufacturing activity.
Status
Dates, surveillance, renewals, and current standing require verification.
Third-party certification
Current Cosmetic Manufacturing Certifications
These documents identify Zhuhai RiXin Cosmetics Co., Ltd. as the holder and apply only to the location, scope, and conditions stated on each certificate.
ISO 22716:2007 Cosmetics Good Manufacturing Practices
- Record type
- Third-party certification
- Certificate holder
- Zhuhai RiXin Cosmetics Co., Ltd.
- Certified location
- 2–6/F, Rixin Building, No. 1 Futian Road, Xiangzhou District, Zhuhai City, Guangdong Province, China
- Certified scope
- General liquid manufacturing for hair-care and cleansing products, skincare liquids and gels; and cream-and-lotion manufacturing for skincare, cleansing, and hair-care products, as stated on the certificate
- Certification body
- DEKRA Testing and Certification (Shanghai) Ltd. / Hangzhou DEKRA Certification Co., Ltd.
- Certificate number
- DH2025GMP(B)0107
- Certificate period shown
- September 21, 2025 to September 20, 2028
- Continued-validity condition
- The certificate states that annual surveillance audits are required
ISO 22716 addresses production, control, storage, and shipment of cosmetics. The certificate supports review of the stated manufacturing scope; it does not certify every product or replace project-level assessment.
Cosmetic Good Manufacturing Practice Certification
- Record type
- Third-party certification
- Certificate holder
- Zhuhai RiXin Cosmetics Co., Ltd.
- Certified location
- 2–6/F, Rixin Building, No. 1 Futian Road, Xiangzhou District, Zhuhai City, Guangdong Province, China
- Certified scope
- General liquid, gel, cream, and lotion manufacturing categories for the skincare, cleansing, and hair-care products stated on the certificate
- Certification body
- DEKRA Testing and Certification (Shanghai) Ltd. / Hangzhou DEKRA Certification Co., Ltd.
- Certificate number
- DH2025GMP(D)0107
- Certificate period shown
- September 21, 2025 to September 20, 2028
- Continued-validity condition
- The certificate states that annual surveillance audits are required
This record supports review of the GMP system and scope shown. It is not a guarantee of safety, efficacy, compliance, retailer acceptance, or market authorization.
Registration record
U.S. Cosmetic Facility Registration
U.S. FDA Cosmetic Facility Registration
- Record type
- Facility Registration — Not a Certification
- Registered facility
- Zhuhai Rixin Cosmetics Co., Ltd.
- Facility address shown
- No. 1 Futian Road, Zhuhai, Guangdong, China 519000
- Business type shown
- Manufacturer
- FEI
- 3037703203
- Reference date shown on the available third-party document
- November 8, 2025
- Current status
- Must be confirmed against the active registration record before publication
FDA does not issue certificates for cosmetic facility registrations or product listings. Registration is not FDA approval, certification, or endorsement, and it does not establish that a specific product, formula, label, or claim complies with U.S. requirements.
Scope and limitations
What These Records Do—and Do Not—Establish
Depending on the record, the documents may show that a named entity and facility were reviewed against a stated manufacturing-practice scheme, or that facility information was registered under an applicable framework. They do not establish finished-product approval, safety, efficacy, stability, package compatibility, claim substantiation, label acceptance, import authorization, retailer approval, or compliance in every market. Project-level testing, documentation, and market review remain separate.
Connected capability
Review Certifications With the Relevant Capability
Manufacturing Facility
Review the facility, production areas, equipment, operations, filling, and traceability connected to the certified location.
View the Manufacturing FacilityQuality, Testing & Documentation
Review project-specific checks, tests, specifications, reports, and documents not established by facility certifications.
Review Quality and DocumentationProject Requirements
Define the product, market, quantity, packaging, claims, retailer requirements, and required certification or audit program.
Prepare Project RequirementsProject Qualification
Review Certification Requirements for Your Project
Share your product category, market, quantity, retailer or importer requirements, required records, and timeline. We will review which manufacturing certifications, facility records, project documents, and additional checks are relevant.