The "Measures for the Administration of Cosmetics Registration and Filing" have been reviewed and adopted by the 14th Bureau Meeting of the State Administration for Market Regulation in 2020 on December 31, 2020, and are hereby promulgated and will come into force as of May 1, 2021.

 

Measures for the administration of cosmetics registration and filing

(Promulgated by Order No. 35 of the State Administration for Market Regulation on January 7, 2021)

Chapter I General rules

Article 1 In order to regulate the registration and filing of cosmetics and ensure the quality and safety of cosmetics, these Measures are formulated in accordance with the Regulations on the Supervision and Administration of Cosmetics.

Article 2 These Measures shall apply to the registration, filing and supervision of cosmetics and new raw materials within the territory of the People's Republic of China.

Article 3 The registration of cosmetics and cosmetics new raw materials refers to the activities in which the applicant for registration submits an application for registration in accordance with legal procedures and requirements, and the drug regulatory department examines the safety and quality controllability of the cosmetics and cosmetics new raw materials applied for registration and decides whether to approve the application.

The filing of cosmetics and cosmetics new raw materials refers to the activities in which the filing person submits information indicating the safety and quality controllability of cosmetics and cosmetics new raw materials in accordance with legal procedures and requirements, and the drug regulatory department files the submitted information for reference.

Article 4 The State applies registration management to special cosmetics and new raw materials of cosmetics with high risk, and archival management to ordinary cosmetics and other new raw materials of cosmetics.

Article 5 The State Drug Administration shall be responsible for the registration and filing administration of special cosmetics, imported general cosmetics and new raw materials for cosmetics, and shall guide and supervise the work related to the filing of cosmetics undertaken by the drug regulatory departments of provinces, autonomous regions and municipalities directly under the Central Government. The State Drug Administration may entrust drug regulatory departments of provinces, autonomous regions and municipalities directly under the Central Government with corresponding capabilities to implement the registration and administration of imported general cosmetics.

The cosmetic Technical review agency of the State Drug Administration (hereinafter referred to as the technical review agency) is responsible for the technical review of the registration of special cosmetics and cosmetics new raw materials, the technical verification of imported ordinary cosmetics and cosmetics new raw materials after filing, and the evaluation of the use and safety report of new cosmetic raw materials.

The National Drug Administration administrative matters acceptance service agency (hereinafter referred to as the acceptance agency), audit and inspection agency, adverse reaction monitoring agency, information management agency and other professional and technical institutions, undertake the registration acceptance, on-site verification, adverse reaction monitoring, information construction and management required for the registration and filing management of cosmetics.

Article 6 The drug regulatory departments of provinces, autonomous regions and municipalities directly under the Central Government shall be responsible for the record administration of domestic ordinary cosmetics within their respective administrative areas, and shall implement the record administration of imported ordinary cosmetics in the name of the State Drug Administration within the entrusted scope, and assist in the on-site verification of the registration of special cosmetics.

Article 7 Registrants and recordholders of cosmetics and cosmetics new raw materials shall fulfill the obligations of product registration and recordkeeping according to law, and be responsible for the quality and safety of cosmetics and cosmetics new raw materials.

The registrant or recordholder of cosmetics and new raw materials shall, when applying for registration or filing, comply with the requirements of relevant laws, administrative regulations, mandatory national standards and technical norms, and be responsible for the authenticity and scientific nature of the materials submitted.

Article 8 Where the registrant or record holder is outside China, an enterprise legal person within China shall be designated as the responsible person within China. The domestic responsible person shall perform the following obligations:

(1) Handle the registration and filing of cosmetics and cosmetics new raw materials in the name of the registrant or recordholder;

(2) Assist registrants and recordholders to carry out adverse reaction monitoring of cosmetics and safety monitoring and reporting of new raw materials of cosmetics;

(3) Assist registrants and recordholders in implementing the recall of cosmetics and cosmetics new raw materials;

(4) In accordance with the agreement with the registrant and the recordholder, undertake the corresponding quality and safety responsibility for the cosmetics and new raw materials of cosmetics put on the domestic market;

(5) Cooperate with the supervision and inspection work of the drug regulatory department.

Article 9 The drug regulatory department shall, within 5 working days from the date on which cosmetics and new raw materials of cosmetics are approved for registration and the filing is completed, publish the relevant information on the registration and filing management of cosmetics and new raw materials of cosmetics to the public for public inquiry.

Article 10 The State Medical Products Administration shall strengthen the construction of information technology and provide facilitation services for registrants and record holders.

Cosmetics and cosmetics new raw materials registrants and recordholders apply for registration and record filing through the cosmetics and cosmetics new raw materials registration information service platform (hereinafter referred to as the information service platform) in accordance with regulations.

The State Medical Products Administration has formulated a catalogue of used cosmetic raw materials, which is updated in a timely manner and disclosed to the public for the convenience of enterprises.

Article 11 The drug regulatory department may establish an expert consultation mechanism to listen to the opinions of experts on important issues in the process of technical review, on-site verification, supervision and inspection, and give play to the technical support role of experts.

 

Chapter II Cosmetics new raw materials registration and record management

Section 1 Registration and filing of new cosmetic raw materials

Article 12 Natural or artificial raw materials first used in cosmetics in China shall be new raw materials for cosmetics.

Adjusting the purpose of use, safe use of cosmetic raw materials, etc., shall apply for registration and record in accordance with the requirements for new raw materials registration and record keeping.

Article 13 To apply for registration of new cosmetic raw materials with anti-corrosion, sunscreen, coloring, hair coloring, freckle whitening functions, the application materials shall be submitted in accordance with the requirements of the State Drug Administration. The accepting institution shall, within 5 working days from the date of receipt of the application, complete the formal examination of the application materials and deal with them according to the following circumstances:

(1) If the application does not need to be registered according to law, it shall make a decision to reject the application and issue a notice of rejection;

(2) If the application does not fall within the scope of the functions and powers of the State Drug Administration according to law, it shall make a decision to reject the application, issue a notification of rejection, and inform the applicant to apply to the relevant administrative organ;

(3) Where the application materials are not complete or do not conform to the prescribed form, a notice of correction shall be issued to inform the applicant of all the contents to be corrected at one time, and if the applicant fails to notify the applicant within the time limit, the application shall be accepted from the date of receipt of the application materials;

(4) Where the application information is complete and meets the requirements of the prescribed form, or the applicant submits all the supplementary materials as required, the application for registration shall be accepted and a notice of acceptance shall be issued.

The acceptance institution shall, within 3 working days after accepting the registration application, transmit the application materials to the technical review institution.

Article 14 The technical review institution shall, within 90 working days from the date of receiving the application materials, organize the technical review in accordance with the requirements of the technical review, and deal with the following situations:

(1) If the application information is true and complete, can prove the safety and quality control of raw materials, and meets the requirements of laws, administrative regulations, mandatory national standards and technical specifications, the technical review agency shall make the review conclusion that the technical review has passed;

(b) the application information is not true, can not prove the safety of raw materials, quality control, does not meet the requirements of laws, administrative regulations, mandatory national standards and technical specifications, the technical review agency shall make the technical review fails to pass the review conclusion;

(3) If the applicant needs to supplement the information, it shall inform all the contents that need to be supplemented at one time; The applicant shall provide supplementary information within 90 working days as required, and the review time limit shall be recalculated after the technical review institution receives the supplementary information; If the supplementary information is not provided within the prescribed time limit, the technical review institution shall make the review conclusion that the technical review is not passed.

Article 15 If the conclusion of the technical review is not passed, the technical review institution shall inform the applicant and explain the reasons. If the applicant has any objection, it may apply for a review within 20 working days from the date of receiving the conclusion of the technical review. The content of the review is limited to the original application items and application materials.

The technical review institution shall make the review conclusion within 30 working days from the date of receiving the review application.

Article 16 The State Drug Administration shall, within 20 working days from the date of receipt of the technical review conclusions, review the legality, standardization and integrity of the technical review procedures and conclusions, and make a decision on whether to grant registration.

The acceptance agency shall, within 10 working days from the date of the SDA's decision on administrative approval, issue the registration certificate of new cosmetic raw materials to the applicant or the decision not to register.

Article 17 Before the technical review agency makes a technical review conclusion, the applicant may file an application for withdrawal of registration. In the process of technical review, if suspected of providing false information or there are safety problems with new raw materials of cosmetics, the technical review agency shall handle it according to law, and the applicant shall not withdraw the application for registration.

Article 18 The recordholder of new cosmetic raw materials shall complete the filing after submitting the materials as required by the State Drug Administration.

 

Section II Safety monitoring and reporting

Article 19 A safety monitoring system shall be implemented for new cosmetic raw materials that have been registered and completed the filing. The period of safety monitoring shall be 3 years, counting from the date of obtaining registration or completing the filing of cosmetics using new raw materials for the first time.

Article 20 Within the period of safety monitoring, the registrant and record holder of new cosmetic raw materials may use the new cosmetic raw materials to produce cosmetics.

Cosmetic registrants and recordholders use new raw materials to produce cosmetics, and the relevant cosmetics shall be confirmed by the registrant and recordholder of new raw materials through the information service platform when applying for registration and handling the record.

Article 21 The registrant and record holder of new cosmetic raw materials shall establish a safety risk monitoring and evaluation system for new cosmetic raw materials after they are listed, conduct follow-up research on the safety of new cosmetic raw materials, and conduct continuous monitoring and evaluation on the use and safety of new cosmetic raw materials.

The registrant and record holder of new cosmetic raw materials shall summarize and analyze the use and safety of new cosmetic raw materials within 30 working days before the completion of each year of safety monitoring of new cosmetic raw materials, and form an annual report to the State Drug Administration.

Article 22 If the following circumstances are found, the registrant and record holder of the new raw materials of cosmetics shall immediately carry out research and report to the technical review institution:

(A) other countries (regions) found that the use of similar raw materials caused serious adverse reactions to cosmetics or group adverse reactions;

(2) The cosmetic laws, regulations and standards of other countries (regions) raise the standards for the use of the same raw materials, increase the use of restrictions or prohibit the use;

(3) Other situations related to the safety of new cosmetic raw materials.

If there is evidence that there are safety problems with new raw materials of cosmetics, the registrant and record holder of new raw materials of cosmetics shall take immediate measures to control risks and report to the technical review agency.

Article 23 Cosmetics registrants and recordholders who use new raw materials to produce cosmetics shall timely report the use and safety of new raw materials to the registrants and recordholders of new raw materials.

In the event of adverse reactions or safety problems that may be related to new cosmetic raw materials, the cosmetic registrant or recordholder shall immediately take measures to control risks, notify the registrant or recordholder of new cosmetic raw materials, and report to the drug regulatory department of the province, autonomous region or municipality directly under the Central Government in accordance with regulations.

Article 24 The drug regulatory department of a province, autonomous region or municipality directly under the Central Government shall, after receiving a report on cosmetic adverse reactions or safety problems caused by the use of new cosmetic raw materials, organize research and analysis, and consider that new cosmetic raw materials may cause human injury or endanger human health and other safety risks, shall take measures to control the risks in accordance with relevant provisions. And immediately feedback to the technical review body.

25th technical review institutions received provincial, autonomous region, municipality directly under the central Government of the drug regulatory department or registrants of new cosmetic raw materials, the feedback or report, should be combined with adverse reaction monitoring institutions annual adverse reaction statistical analysis results of cosmetics assessment, it is considered that by adjusting the technical requirements of new cosmetic raw materials can eliminate safety risks, It may propose suggestions for adjustment and report them to the State Drug Administration; If it is considered that there are safety problems, it shall be reported to the State Drug Administration for cancellation of registration or cancellation of the record. The SDA shall make a decision without delay.

Article 26 Three years after the expiration of the safety monitoring of new cosmetic raw materials, the technical review institution shall put forward to the State Drug Administration whether the new cosmetic raw materials meet the safety requirements.

For new cosmetic raw materials with safety problems, the State Drug Administration shall cancel the registration or cancel the record; If there are no safety problems, the State Drug Administration shall incorporate them into the catalogue of used cosmetic raw materials.

27th safety monitoring period is ordered to suspend the use of new raw materials of cosmetics, cosmetics registrants, record holders should be suspended at the same time, the use of the new raw materials of cosmetics cosmetics.

 

Chapter III cosmetics registration and filing management

Section 1 General requirements

Article 28 Cosmetics registration applicants and record holders shall meet the following conditions:

(1) Enterprises or other organizations established according to law;

(2) there is a quality management system suitable for applying for registration and filing cosmetics;

(3) Have the ability to monitor and evaluate adverse reactions.

Where the registration applicant applies for the registration of special cosmetics for the first time or the filing person for the record of ordinary cosmetics for the first time, it shall submit the certification materials that it meets the requirements of the preceding paragraph.

Article 29 Cosmetics registrants and recordholders shall, in accordance with laws, administrative regulations, mandatory national standards, technical specifications and registration and recordkeeping management provisions, carry out cosmetic development, safety assessment, registration and recordkeeping inspection, and submit registration and recordkeeping materials in accordance with the requirements of the cosmetic registration and recordkeeping materials specification.

Article 30 The registrant and recordholder of cosmetics shall select the raw materials that meet the requirements of laws, administrative regulations, mandatory national standards and technical specifications for the production of cosmetics, and be responsible for the safety of the raw materials used. Cosmetics registrants and recordholders shall, when applying for registration and filing, clarify the source of raw materials and relevant information about raw material safety through the information service platform.

Article 31 Where a cosmetics registrant or record holder entrusts the production of cosmetics, domestic cosmetics shall, when applying for registration or filing, be confirmed by the cosmetics manufacturer through the information service platform; Imported cosmetics shall be submitted by the registrant and recordholder of cosmetics with relevant materials of entrusted relationship.

Article 32 A cosmetic registrant or recordholder shall clarify the standards for the implementation of the product and submit them to the drug regulatory department when applying for registration or filing.

Article 33 The applicant for cosmetics registration and the recordholder shall entrust the inspection institution that has obtained the qualification recognition and meets the needs of the inspection work for cosmetics registration and recordkeeping to conduct the inspection in accordance with the requirements of the mandatory national standards, technical specifications and the inspection provisions for registration and recordkeeping.

 

Section 2 Record management

Article 34 Before ordinary cosmetics are listed or imported, the filing person shall complete the filing after submitting the filing materials through the information service platform as required by the State Drug Administration.

Article 35 Where the imported ordinary cosmetics that have been filed are to be imported at ports other than the administrative areas of the provinces, autonomous regions and municipalities directly under the Central Government where the responsible person is located, the contact information of the import ports and customs clearance procedures shall be supplemented through the information service platform.

Article 36 For ordinary cosmetics that have been put on record, the name of the product shall not be changed without good reason. Efficacy claims should not be altered without sufficient scientific evidence.

Ordinary cosmetics that have been filed may not change the product formula at will, except for minor changes in the product formula due to changes in raw material sources and other reasons.

Where the change of the address of the recordholder or the domestic responsible person leads to the change of the recordkeeping administration department, the recordholder shall re-record.

Article 37 The recordholder of ordinary cosmetics shall report annually to the drug supervisory and administrative department responsible for the recordkeeping administration the production and import, as well as the compliance with laws and regulations, mandatory state standards and technical norms.

Where the registered product is no longer produced or imported, the recordholder shall promptly report to the drug regulatory department that undertakes the recordkeeping administration to cancel the recordkeeping.

 

Section 3 Registration Management

Article 38 Before the production or import of special cosmetics, the applicant for registration shall submit application materials in accordance with the requirements of the State Drug Administration.

Where the registration procedures and time limits for special cosmetics are not specified, the provisions of these Measures on the registration of new raw materials for cosmetics shall apply.

Article 39 The technical review institution shall, within 90 working days from the date of receiving the application materials, organize the technical review in accordance with the requirements of the technical review, and deal with it according to the following circumstances:

(a) the application information is true and complete, can prove the product safety and quality control, product formulation and product implementation standards are reasonable, and in line with the current laws, administrative regulations, mandatory national standards and technical specifications requirements, to make the technical review passed the review conclusion;

(b) the application information is not true, can not prove the product safety and quality control, product formulation and product implementation standards are unreasonable, or does not meet the current laws, administrative regulations, mandatory national standards and technical specifications, the technical review fails to pass the review conclusion;

(3) If the applicant needs to supplement the information, it shall inform all the contents that need to be supplemented at one time; The applicant shall provide supplementary information within 90 working days as required, and the review time limit shall be recalculated after the technical review institution receives the supplementary information; If the supplementary information is not provided within the prescribed time limit, the technical review institution shall make the review conclusion that the technical review is not passed.

Article 40 The State Drug Administration shall, within 20 working days from the date of receiving the technical review conclusions, review the legality, standardization and integrity of the technical review procedures and conclusions, and make a decision on whether to grant registration.

The acceptance institution shall, within 10 working days from the date when the SDA makes the decision on administrative approval, issue the cosmetic registration certificate or the decision not to register to the applicant. Cosmetic registration certificate is valid for 5 years.

Article 41 Where the registration items of special cosmetics that have been registered change, the SDA shall implement classified management according to the impact of the changes on the safety and efficacy of the products:

(A) does not involve the safety, efficacy claims change, the registrant shall promptly to the State drug Administration for record;

(2) changes in matters involving safety, as well as substantial changes in the production process, efficacy claims, etc., the registrant shall file an application for product registration change with the State Drug Administration;

(3) Where the product name, formula, etc., has changed and constitutes a new product in essence, the registrant shall apply for registration again.

Article 42 Where a registered product is no longer produced or imported, the registrant shall take the initiative to apply for cancellation of the registration certificate.

 

Section 4 Renewal of Registration Certificate

Article 43 Where a special cosmetic registration certificate needs to be renewed upon expiration, the registrant shall apply for renewal of registration 90 to 30 working days before the expiration of the product registration certificate, and undertake to meet the requirements of mandatory national standards and technical specifications. The registrant shall be responsible for the authenticity and legality of the materials submitted and the commitments made.

If the application for renewal of registration is not submitted within the time limit, the application for renewal of registration will not be accepted.

Article 44 The acceptance institution shall conduct a formal review of the application materials within 5 working days after receiving the application for renewal of registration, and accept those that meet the requirements, and issue a new registration certificate to the applicant within 10 working days from the date of acceptance. The validity period of the registration certificate shall be recalculated from the day following the expiration date of the original registration certificate.

Article 45 The drug regulatory department shall supervise the application materials and commitments of special cosmetics that have been renewed for registration, and shall revoke the registration certificate of special cosmetics according to law if it is found through supervision and inspection or technical review that there is no compliance with compulsory national standards and technical norms.

 

Chapter IV Supervision and administration

Article 46 The drug regulatory department shall, in accordance with the provisions of laws and regulations, supervise and inspect the activities related to the registration and filing of registrants and recordholders, and may, when necessary, conduct extended inspections of the units involved in the registration and recordkeeping activities, and the relevant units and individuals shall cooperate and shall not refuse to inspect or conceal the relevant information.

Article 47 In the process of registered technical review, the technical review institution may notify the examination and verification institution to carry out on-site verification as needed. The domestic on-site verification shall be completed within 45 working days, and the overseas on-site verification shall be implemented in accordance with the relevant regulations on overseas verification. The time spent on on-site verification is not included in the review time limit.

The registration applicant shall cooperate with the on-site verification work, and if sampling inspection is required, the sample shall be provided as required.

Article 48 After obtaining the registration certificate of special cosmetics, the registrant shall upload the label pictures of the products on the market to the information service platform for public inquiry before the products are put on the market.

Article 49 The registration certificate of cosmetics shall not be transferred. Where the principal qualification of the original registrant is cancelled due to legal reasons such as enterprise merger or division, and the registrant is changed to a newly established enterprise or other organization, it shall apply for change of registration in accordance with the provisions of these Measures.

After the change, the registrant shall comply with the provisions of these Measures on registrants, and bear the quality and safety responsibility for the products that have been listed.

Article 50 If, according to the development of scientific research, the understanding of the safety of cosmetics and cosmetics raw materials has changed, or there is evidence that cosmetics and cosmetics raw materials may be defective, the drug regulatory department responsible for registration and filing administration may order the registrant or filing person of cosmetics and cosmetics new raw materials to carry out a safety reassessment. Or directly organize related raw material enterprises and cosmetics enterprises to carry out safety reassessment.

Reassessment results show that cosmetics, cosmetics raw materials can not guarantee safety, by the original registration department to cancel the registration, the record department to cancel the record, by the drug regulatory department under The State Council will be prohibited for the production of cosmetics raw materials into the catalogue of raw materials, and announced to the public.

Article 51 According to the development of scientific research, monitoring and evaluation of cosmetic safety risks, it is found that there are safety risks in cosmetic raw materials, and the safety risks can be eliminated by setting the scope and conditions of use of raw materials, the scope and conditions of restricted use of raw materials should be clearly defined in the catalogue of used cosmetic raw materials.

Article 52 If the drug regulatory department responsible for registration and filing management is unable to contact the registrant, filing person or domestic responsible person through registration and filing information, it may list the registrant, filing person or domestic responsible person as a key object of supervision on the information service platform, and announce it through the information service platform.

Article 53 The drug supervisory and administrative department shall implement risk classification and classification management according to the filing person, the domestic responsible person, the operation of the quality management system of the cosmetic manufacturing enterprise, the supervision after filing, and the supervision and inspection of the product after listing.

Article 54 Drug regulatory departments, technical review, on-site verification, inspection institutions and their staff shall strictly abide by laws, regulations, rules and relevant provisions of the State Drug Administration to ensure that the relevant work is scientific, objective and fair.

Article 55 Without the consent of the registrant and the recordholder, the drug regulatory department, the professional technical institution, its staff, and the personnel participating in the review shall not disclose the trade secrets, undisclosed information or confidential business information submitted by the registrant and the recordholder, except as otherwise provided by law or involving national security or major social and public interests.

 

Chapter V Legal liability

Article 56 Where a registrant of cosmetics or new raw materials of cosmetics fails to apply for the change registration of special cosmetics or new raw materials of cosmetics in accordance with the provisions of these Measures, the original issuing drug regulatory department shall order it to make corrections, give a warning, and impose a fine of not less than 10,000 yuan but not more than 30,000 yuan.

Cosmetics and cosmetics new raw materials recordholder fails to update the record information of ordinary cosmetics and cosmetics new raw materials in accordance with the provisions of these Measures, the drug regulatory department responsible for the record management shall order correction, give a warning, and impose a fine of more than 5,000 yuan and less than 30,000 yuan.

Cosmetics and cosmetics new raw materials registrants who fail to re-register in accordance with the provisions of these measures shall be punished in accordance with the provisions of Article 59 of the Regulations on the Supervision and Administration of Cosmetics; Where the recordholder of cosmetics and cosmetics new raw materials fails to re-record in accordance with the provisions of these Measures, he shall be punished in accordance with the provisions of the first paragraph of Article 61 of the Regulations on the Supervision and Administration of cosmetics.

Article 57 Any registrant or recordholder of new cosmetic raw materials who violates the provisions of Article 21 of these Measures shall be ordered to make corrections by the drug regulatory department of the province, autonomous region or municipality directly under the Central Government; Whoever refuses to make corrections shall be fined not less than 5,000 yuan but not more than 30,000 yuan.

Article 58 Where the drug regulatory department responsible for the record management finds that the record information of cosmetics and new raw materials of cosmetics does not meet the requirements, it shall order correction within a time limit, and where the record information related to the safety of cosmetics and new raw materials of cosmetics does not meet the requirements, it may also order suspension of sales and use.

For cosmetics and new raw materials that have been put on record but whose information has not been released to the public, the drug supervisory and administrative department responsible for the record management finds that the record information does not meet the requirements, it may order the recordholder to correct and release the record information to the public after meeting the requirements.

Article 59 Where the recordholder exists under the following circumstances, the drug supervisory and administrative department responsible for the recordkeeping shall cancel the recordkeeping of cosmetics and new raw materials:

(1) Submitting false information when filing a record;

(2) the materials that have been filed do not meet the requirements, fail to correct within the prescribed time limit as required, or fail to suspend the sale and use of cosmetics and new raw materials for cosmetics as required;

(3) does not belong to the scope of new raw materials of cosmetics or cosmetics filing.

 

Chapter VI Supplementary Provisions

Article 61 The last process of contacting the contents of cosmetics is a domestic product completed in China, an imported product completed outside China, and a reference import product management completed in Taiwan, Hong Kong and Macao of China.

For a combination product or a combination package product that applies for registration or filing under a product name, where the last process of contact with the contents of any dose is completed abroad, it shall be administered as imported products.

Article 62 Cosmetics and new raw materials of cosmetics shall be numbered according to the following rules after they have been registered or filed for the record.

(1) The registration number rules of new raw materials for cosmetics: national makeup original characters + four years + the number of new raw materials for the record this year.

(2) The registration number rules of new cosmetics raw materials: national cosmetics original note + four annual number + the order number of new cosmetics raw materials registered this year.

(3) Ordinary cosmetics record number rules:

Domestic products: provinces, autonomous regions, municipalities + abbreviation + four years + the number of products registered in the administrative region in this year;

Imported products: National makeup network prepared into the word (the province, autonomous region and municipality where the responsible person is located) + four years + this year's national record product sequence number;

China Taiwan, Hong Kong, Macao products: national makeup network prepared word (the responsible person in the province, autonomous region, municipality directly under the central government referred to) + four years + this year's national record product sequence number.

(4) Special cosmetics registration number rules:

Domestic products: Guocuente + four annual number + the number of registered products in this year;

Imported products: Guocuenjin character + four annual number + the number of registered products in this year;

China Taiwan, Hong Kong, Macau products: national makeup special characters + four years + the number of registered products in this year.

Article 63 These Measures shall come into force as of May 1, 2021.