A Comprehensive Guide to China's Cosmetic Regulations in 2025
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2025 Annual Overview of Regulatory Dynamics
No | Issuing Authority | Announcement Date | Regulation Content | Effective Date |
1 | NIFDC | 2025/1/22 | NIFDC's Notice on Publicly Soliciting Comments on 9 Testing Methods Including "In Vitro Skin Absorption Test (Draft for Comments)" | Before 2025/2/21 |
2 | NMPA | 2025/1/26 | NMPA Announcement on Issuing Several Provisions Supporting Cosmetic Ingredient Innovation (No. 12, 2025) | 2025/1/26 |
3 | NIFDC | 2025/2/9 | NIFDC Notice on Updating the "Information on the Use of Ingredients in Marketed Products" | 2025/2/9 |
4 | NIFDC | 2025/2/19 | NIFDC's Notice on Publicly Soliciting Comments on "Usage Information for Some Ingredients Included in the International Cosmetic Ingredient Safety Review Data Index (Draft for Comments)" | Before 2025/3/4 |
5 | NIFDC | 2025/3/28 | NIFDC's Notice on Publicly Soliciting Comments on the "Technical Guideline for Updating Cosmetic New Ingredient Filing Information (Draft for Comments)" | Before 2025/4/15 |
6 | NMPA | 2025/4/9 | NMPA Announcement on Issuing the "Measures for the Administration of Cosmetic Safety Risk Monitoring and Evaluation" (No. 37, 2025) | 2025/8/1 |
7 | NIFDC | 2025/4/10 | NIFDC Notice on Issuing the "Usage Information for Some Ingredients Included in the International Cosmetic Ingredient Safety Review Data Index" | 2025/4/10 |
8 | NMPA | 2025/4/29 | NMPA Announcement on Issuing the Supplementary Cosmetic Testing Method for "Determination of Methylprednisolone in Cosmetics" (No. 47, 2025) | 2025/4/29 |
9 | NMPA | 2025/5/6 | NMPA Notice on Incorporating 7 Methods Including the Test Method for Excessive Hard Particles in Toothpaste into the "Safety and Technical Standards for Cosmetics (2015 Edition)" (No. 18, 2025) | 2026/3/1 |
10 | NIFDC | 2025/5/6 | NIFDC Notice on Re-soliciting Suggestions for Cosmetic Standard Project Proposals for 2025 | Before 2025/5/25 |
11 | NIFDC | 2025/5/9 | NIFDC Notice on Launching the Function Module for Synchronized Declaration of Cosmetic New Ingredients and Associated Products | 2025/5/9 |
12 | Guangzhou MPA | 2025/6/5 | Notice of Guangdong Medical Products Administration on Matters Related to Data Migration of the Domestic Toothpaste Filing Information Management Platform | 2025/6/16 |
13 | Jiangxi MPA | 2025/6/16 | Notice of Jiangxi Provincial Medical Products Administration on Issuing the "Administrative Penalty Discretion Benchmark for Drugs, Medical Devices, and Cosmetics in Jiangxi Province" (2025 Revised Edition) | 2025/8/1 |
14 | NMPA | 2025/6/24 | NMPA Announcement on Matters Concerning the Administration of the "Inventory of Used Cosmetic Ingredients" (No. 61, 2025) | 2025/6/24 |
15 | NIFDC | 2025/6/24 | NIFDC Notice on Issuing 2 Technical Guidelines Including the "Guideline for Research and Determination of Safe Use History of Cosmetic New Ingredients (Trial)" | 2025/6/24 |
16 | NIFDC | 2025/6/24 | NIFDC's Notice on Publicly Soliciting Comments on 9 Cosmetic Standards Including "General Principles for Physical and Chemical Testing Methods (Draft for Comments)" | Before 2025/7/15 |
17 | Beijing MPA | 2025/6/27 | Announcement of Beijing Municipal Medical Products Administration on Issuing the "Guidelines for Publishing Cosmetic Advertisements in Beijing" | 2025/6/25 |
18 | NIFDC | 2025/7/3 | NIFDC's Notice on Publicly Soliciting Comments on 3 Cosmetic Standards Including "Human Skin Patch Test Method (Draft for Comments)" | Before 2025/7/21 |
19 | Zhejiang MPA | 2025/7/16 | Notice of Zhejiang Provincial Medical Products Administration on Issuing the "Measures for Credit Evaluation Management of Cosmetic Registrants, Filers, and Contract Manufacturers in Zhejiang Province" | 2025/7/9 |
20 | NMPA | 2025/7/30 | Public Notice by the General Department of NMPA on the 2025 Cosmetic Standard Project Plan | Before 2025/8/7 |
21 | NIFDC | 2025/7/30 | NIFDC's Public Solicitation of Comments on 3 Cosmetic Standards Including "Test Method for Diethylene Glycol in Cosmetics (Draft for Comments)" | Before 2025/8/20 |
22 | NIFDC | 2025/7/31 | NIFDC's Notice on Publicly Soliciting Comments on 6 Guiding Principles Including the "Technical Guiding Principle for Research on Hair Dye Cosmetics (Trial) (Draft for Comments)" | Before 2025/8/15 |
23 | NMPA | 2025/8/21 | Notice of the General Department of NMPA on Issuing the 2025 Cosmetic Standard Project Plan | 2025/8/21 |
24 | NMPA | 2025/8/29 | NMPA Announcement on Incorporating 5 Methods Including the Bovine Corneal Opacity and Permeability Test Method into the Safety and Technical Standards for Cosmetics | 2026/3/1 |
25 | NIFDC | 2025/9/5 | NIFDC's Notice on Publicly Soliciting Comments on 2 Guiding Principles Including the "Technical Guiding Principle for Research on Anti-hair Loss Cosmetics (Trial) (Draft for Comments)" | Before 2025/9/20 |
26 | NIFDC | 2025/9/15 | NIFDC's Notice on Publicly Soliciting Comments on 18 Cosmetic Standards Including "Microbial Limit for Eye Area Cosmetics, Lip Cosmetics, and Children's Cosmetics (Draft for Comments)" | Before 2025/10/9 |
27 | NMPA | 2025/9/17 | Notice of the General Department of NMPA on Launching the Second Phase Pilot Work for Personalized Cosmetic Services | 2025/10/1 |
28 | NMPA | 2025/9/19 | Public Solicitation of Comments by the General Department of NMPA on "NMPA's Opinions on Deepening Cosmetic Regulatory Reform to Promote High-Quality Industry Development (Draft for Comments)" | Before 2025//10/10 |
29 | NIFDC | 2025/9/24 | NIFDC's Notice on Publicly Soliciting Comments on the "General Technical Rules for Registration and Filing Dossiers of Cosmetic New Ingredients (Draft for Comments)" | Before 2025/10/19 |
30 | NMPA | 2025/9/26 | Public Solicitation of Comments by the General Department of NMPA on "NMPA Announcement on Matters Concerning Toothpaste Filing Management (Draft for Comments)" | Before 2025/10/26 |
31 | NIFDC | 2025/10/14 | NIFDC's Notice on Publicly Soliciting Comments on 6 Cosmetic Standards Including "90-Day Oral Toxicity Test Method (Draft for Comments)" | Before 2025/11/7 |
32 | NMPA | 2025/10/20 | NMPA Notice on Launching Pilot Work for Cosmetic Electronic Labels | 2026/2/1 |
33 | NMPA | 2025/10/20 | NMPA Announces the Inclusion of Three Cosmetic New Ingredients Including Lauroyl Alanine into the "Inventory of Used Cosmetic Ingredients" | 2025/10/20 |
34 | NMPA | 2025/10/20 | Public Notice on the Selection Results of Guidance Varieties for Cosmetic New Ingredient Innovation by the NIFDC | Before 2025/10/24 |
35 | NMPA | 2025/10/31 | NMPA Approves Registration of Two New Cosmetic Ingredients | 2025/10/31 |
36 | NMPA | 2025/11/17 | NMPA's Opinions on Deepening Cosmetic Regulatory Reform to Promote High-Quality Industry Development | 2025/11/17 |
37 | NIFDC | 2025/11/17 | NIFDC's Notice on Publicly Soliciting Comments on 3 Cosmetic Standards Including "Mercury and Its Compounds (Draft for Comments)" | Before 2025/12/12 |
38 | NMPA | 2025/12/1 | Public Solicitation of Comments by the General Department of NMPA on the "Toothpaste Classification Catalog (Draft for Comments)" | Before 2025/12/22 |
39 | NIFDC | 2025/12/11 | NIFDC's Public Solicitation of Comments on 2 Guiding Principles Including the "Technical Guiding Principle for Naming Plant-derived Cosmetic New Ingredients (Draft for Comments)" | Before 2025/12/26 |
40 | NMPA | 2025/12/12 | Notice of the General Department of NMPA on Issuing the Three-Year Action Plan for Improving the Production Quality Management System of Cosmetic Enterprises (2026-2028) | 2025/12/12 |
41 | NIFDC | 2025/12/12 | NIFDC Notice on Soliciting Suggestions for Cosmetic Standard Project Proposals for 2026 | Before 2026/1/15 |
42 | NIFDC | 2025/12/15 | NIFDC Notice on Issuing the "Technical Guideline for Updating Cosmetic New Ingredient Filing Information" | 2025/12/15 |
43 | NIFDC | 2025/12/16 | NIFDC Notice on Issuing 2 Cosmetic Technical Guiding Principles Including the "Technical Guiding Principle for Research on Anti-hair Loss Cosmetics (Trial)" | 2025/12/16 |
44 | NIFDC | 2025/12/19 | NIFDC Notice on Issuing the "Technical Guideline for Cosmetic Ingredient Intended Use (Trial)" | 2026/6/19 |
45 | NMPA | 2025/12/23 | NMPA Announcement on Matters Concerning Toothpaste Filing Management (No. 124, 2025) | 2025/12/1 |
46 | Guangzhou MPA | 2025/12/24 | Announcement of Guangdong Medical Products Administration on Launching Pilot Work for Cosmetic Electronic Labels | 2026/2/1 |
47 | NMPA | 2025/12/24 | Public Solicitation of Comments by the General Department of NMPA on the "Provisions on the Administration of Registration and Filing Dossiers for Cosmetic New Ingredients (Revised Draft for Comments)" | Before 2026/1/25 |
1. Usage Information for Some Ingredients Listed in the International Cosmetic Ingredient Safety Review Data Index
Release Date: April 10, 2025
Issuing Authority: National Institutes for Food and Drug Control (NIFDC)
Key Points Interpretation:
The release of the "Usage Information for Some Ingredients Included in the International Cosmetic Ingredient Safety Review Data Index" is a concrete implementation of the NMPA's Announcement No. 50 of 2024, "Several Measures for Optimizing the Administration of Cosmetic Safety Assessment." This document systematically consolidates the actual usage data of specific ingredients within China's registered/filed products, focusing on those lacking clear safety conclusions or having restricted usage conditions in authoritative international indices. It aims to provide the industry with crucial "localized" safety evidence references, bridging the gap between international data and domestic regulatory requirements. This helps companies obtain more direct and regulator-recognized data support when conducting safety assessments for these ingredients, thereby enhancing the scientific validity and reliability of assessment reports.
2. Full Implementation of the Complete Version of Cosmetic Safety Assessment (Section 5.1)
Implementation Date: May 1, 2025
Issuing Authority: National Medical Products Administration (NMPA)
Key Points Interpretation:
In 2021, the NMPA issued the Technical Guidelines for Cosmetic Safety Assessment (2021 Edition), explicitly requiring companies to submit a complete safety assessment report as compliance documentation. In April 2024, to further optimize administration, the NMPA released the Several Measures for Optimizing the Administration of Cosmetic Safety Assessment. Considering the long R&D cycle for cosmetics, to avoid redundant investment of R&D resources by companies, it allowed cosmetic registrants/filers to continue using a simplified version of the safety assessment report that met the Guidelines requirements when applying for registration or filing until May 1, 2025. This means that from May 1, 2025, onwards, the system for the complete version of the cosmetic safety assessment will be fully implemented. Companies can no longer use the previous simplified reports and must submit the complete assessment materials as stipulated.
3. Tiered Management / Dynamic Update of the Inventory of Used Cosmetic Ingredients
Release Date: June 24, 2025
Issuing Authority: National Medical Products Administration (NMPA)
Key Points Interpretation:
This represents a major reform of the foundational system for ingredient management. The new regulation splits the inventory into "Inventory I" (an optimized version of the original Inventory) and "Inventory II" (cosmetic new ingredients transferred upon completion of their safety monitoring period), achieving differentiated and refined control over new and existing ingredients. The most significant technical adjustment is the removal of the "Maximum Historical Usage in Products" column, emphasizing that companies must complete safety assessments based on scientific evidence rather than simply relying on historical usage levels. Concurrently, the NMPA explicitly stated it will establish a dynamic update mechanism. Future information regarding supplements, errata, etc., for the inventory will be disclosed in real-time via its official website. Companies must proactively monitor this to ensure the timeliness and accuracy of information for the ingredients they use.
4. Guidelines for Research and Determination of Safe Use / Food Use History of New Ingredients
Release Date: June 24, 2025
Issuing Authority: National Institutes for Food and Drug Control (NIFDC)
Key Points Interpretation:
To complement the Several Provisions Supporting Cosmetic Ingredient Innovation, the NIFDC released the Guideline for Research and Determination of Safe Use History of Cosmetic New Ingredients (Trial) and the Guideline for Research and Determination of Safe Food Use History of Cosmetic New Ingredients (Trial). These two guidelines provide specific research pathways, evaluation methods, and determination principles for the most critical "safe history" evidence required in the registration/filing of cosmetic new ingredients. The documents detail how companies can systematically demonstrate the background of an ingredient's safe application in cosmetics or food through literature research, post-market surveillance data, etc. This provides clear technical guidance for new ingredient applications, reducing uncertainty in R&D and registration.
5. NIFDC Simultaneously Solicits Comments on 18 Cosmetic Technical Standards
Release Date: September 15, 2025
Issuing Authority: National Institutes for Food and Drug Control (NIFDC)
Key Points Interpretation:
This large-scale solicitation for comments on standard development and revision involves multiple dimensions, signaling an important round of technical standard upgrades. The proposed changes include: intending to set stricter microbial limits for cosmetics intended for the eye area, lips, and children; intending to tighten the limit for the harmful substance "1,4-dioxane" in cosmetics; intending to add 7 substances including 6-Amino-m-cresol as prohibited components in cosmetics; and re-evaluating and adjusting the usage scope and concentration of salicylic acid, certain permitted preservatives, sunscreens, and hair dyes. These changes directly relate to product formulation compliance, production process control, and finished product quality control strategies.
6. Official Launch of the Second Phase Pilot for Personalized Cosmetic Services
Release Date: September 17, 2025
Issuing Authority: National Medical Products Administration (NMPA)
Key Points Interpretation:
Building on the experience from the initial pilot phase, the NMPA decided to launch a two-year second-phase pilot in 14 provinces/regions/municipalities, including Tianjin, Shanghai, Zhejiang, and Guangdong. This new phase allows filers, within their offline exclusive stores or directly-operated stores, to perform on-site, small-batch simple mixing and filling of two or more already-filed general cosmetics based on consumers' personalized needs. The document clarifies the principles of "demand-oriented, safety-controlled, and orderly regulation" and includes detailed pilot work requirements. It emphasizes that participating companies must integrate the service location into their quality management system and establish dedicated management protocols to ensure quality and safety risks are controlled throughout the personalized service process.
7. Publication of the First Batch of Selected Guidance Varieties for Cosmetic New Ingredient Innovation
Release Date: October 20, 2025
Issuing Authority: National Institutes for Food and Drug Control (NIFDC)
Key Points Interpretation:
This marks the first time the regulatory authority has explicitly offered "one-on-one" innovation guidance and services for the R&D of specific new ingredients in the form of a published list. The list selects 16 ingredient varieties from four strategic directions: "first-to-market, China-specific characteristics, domestic substitution, and green/low-carbon." Selected ingredients will receive proactive intervention and guidance throughout the process. This list not only indicates key R&D directions for ingredient developers but also previews future innovative components available for downstream cosmetic companies. It serves as an important window for observing industry technological frontiers and regulatory support priorities.
8. NMPA Deploys Pilot Work for Cosmetic Electronic Labels
Release Date: October 20, 2025
Issuing Authority: National Medical Products Administration (NMPA)
Key Points Interpretation:
The pilot work will be launched first in six provinces/municipalities—Beijing, Shanghai, Zhejiang, Shandong, Guangdong, and Chongqing—on February 1, 2026, for a duration of three years. The document formally grants legal status to cosmetic electronic labels, defining them as an integral part of the cosmetic label. Concurrently, key technical documents such as the Cosmetic Electronic Label Data Set and the Technical Specification for Cosmetic QR Codes were released, establishing unified requirements for the information content of electronic labels and the generation/use of QR codes. This initiative aims to leverage digital means to address issues with traditional paper labels, such as limited information capacity, difficulty in updating, and inconvenience for elderly readers, representing a significant step towards intelligent and green cosmetic label management.
9. NMPA Releases 24-Point Opinion on Deepening Regulatory Reform to Promote Industry Development
Release Date: November 17, 2025
Issuing Authority: National Medical Products Administration (NMPA)
Key Points Interpretation:
As a guiding document governing cosmetic regulation and industry development for the next five to ten years, the Opinions systematically proposes 24 specific reform measures. Its core lies in balancing high-quality development with a high level of safety. The content covers: encouraging innovation (e.g., supporting new efficacy cosmetics, new product launches, silver economy); optimizing administration (e.g., streamlining registration/filing dossier requirements, sharing efficacy evaluation data, optimizing safety assessment); strengthening supervision (e.g., promoting tiered and classified supervision of enterprises, enhancing "online governance of online activities"); and technical support and international alignment. This document outlines a clear path for regulatory evolution and an industrial development blueprint, forming the top-level design framework that all cosmetic companies must follow when formulating medium- to long-term strategies.
10. NIFDC Releases Technical Guideline for Updating Cosmetic New Ingredient Filing Information
Release Date: December 15, 2025
Issuing Authority: National Institutes for Food and Drug Control (NIFDC)
Key Points Interpretation:
As an important supporting document for implementing the policies supporting ingredient innovation, this guideline provides clear operational procedures for registrants/filers of already-marketed new ingredients to update information. It specifies in detail how companies should submit updated materials when key information such as production processes or quality control requirements changes during the ingredient's safety monitoring period or after its completion. This aims to establish a dynamic archive management system for the entire lifecycle of new ingredients, ensuring the compliance and traceability of post-market changes. It encourages technological innovation and process optimization while strengthening ongoing safety supervision.
2025 Annual Overview of Cosmetic Testing Method Updates
This year's updates to testing methods span multiple areas, including toxicological safety testing, physicochemical testing, and specialized testing for toothpaste. These provide businesses with clearer and more advanced technical tools for product safety assessment and quality control.
No | Issuing Authority | Announcement Date | Testing Method | Effective Date | Status |
1 | NIFDC | 2025/1/22 | In Vitro Skin Absorption Test | / | Draft for Comments |
2 | NIFDC | 2025/1/22 | Bovine Corneal Opacity and Permeability Test | / | Draft for Comments |
3 | NIFDC | 2025/1/22 | Collagen Gel - Eye Irritation Test | / | Draft for Comments |
4 | NIFDC | 2025/1/22 | In Vitro Chemical Method for Skin Sensitization: Kinetic Direct Peptide Reactivity Assay | / | Draft for Comments |
5 | NIFDC | 2025/1/22 | Immunotoxicity Test Method | / | Draft for Comments |
6 | NIFDC | 2025/1/22 | Test Method for 43 Elements Including Lithium in Cosmetics and Toothpaste | / | Draft for Comments |
7 | NIFDC | 2025/1/22 | Test Method for Total Fluoride in Toothpaste | / | Draft for Comments |
8 | NIFDC | 2025/1/22 | Test Method for Diethylene Glycol and Ethylene Glycol in Toothpaste | / | Draft for Comments |
9 | NIFDC | 2025/1/22 | Test Method for Excessive Hard Particles in Toothpaste | / | Draft for Comments |
10 | NMPA | 2025/4/29 | Determination of Methylprednisolone in Cosmetics | 2025/4/29 | Newly Added |
11 | NMPA | 2025/5/6 | Test Method for Excessive Hard Particles in Toothpaste | 2026/3/1 | Newly Added |
12 | NMPA | 2025/5/6 | Test Method for Diethylene Glycol and Ethylene Glycol in Toothpaste | 2026/3/1 | Newly Added |
13 | NMPA | 2025/5/6 | Test Method for Soluble Fluoride and Free Fluoride in Toothpaste | 2026/3/1 | Newly Added |
14 | NMPA | 2025/5/6 | Test Method for Total Fluoride in Toothpaste | 2026/3/1 | Newly Added |
15 | NMPA | 2025/5/6 | In Vitro Skin Sensitization: ARE-Nrf2 Luciferase LuSens Test Method | 2026/3/1 | Newly Added |
16 | NMPA | 2025/5/6 | Test Method for 43 Elements Including Lithium in Cosmetics | 2026/3/1 | Newly Added |
17 | NMPA | 2025/5/6 | Test Method for 43 Elements Including Lithium in Toothpaste | 2026/3/1 | Newly Added |
18 | NIFDC | 2025/6/24 | General Principles for Physical and Chemical Test Methods | / | Draft for Comments |
19 | NIFDC | 2025/6/24 | Test Method for 6 Ingredients Including Cannabidiol (CBD) in Cosmetics | / | Draft for Comments |
20 | NIFDC | 2025/6/24 | Skin Sensitization: Local Lymph Node Assay: BrdU-FCM | / | Draft for Comments |
21 | NIFDC | 2025/6/24 | Toxicokinetics Test Method | / | Draft for Comments |
22 | NIFDC | 2025/6/24 | General Technical Requirements for Biotechnology-derived Ingredients | / | Draft for Comments |
23 | NIFDC | 2025/6/24 | General Technical Requirements for Plant-derived Ingredients | / | Draft for Comments |
24 | NIFDC | 2025/6/24 | Cosmetic Ingredient - Centella Asiatica Extract | / | Draft for Comments |
25 | NIFDC | 2025/6/24 | Cosmetic Ingredient - Copper Tripeptide-1 | / | Draft for Comments |
26 | NIFDC | 2025/6/24 | Cosmetic Ingredient - Acetyl Hexapeptide-8 | / | Draft for Comments |
27 | NIFDC | 2025/7/3 | Human Skin Patch Test Method | / | Draft for Comments |
28 | NIFDC | 2025/7/3 | Human Safety-in-Use Test Method | / | Draft for Comments |
29 | NIFDC | 2025/7/3 | Human Long-term Safety-in-Use Test Method | / | Draft for Comments |
30 | NIFDC | 2025/7/30 | Test Method for Diethylene Glycol in Cosmetics | / | Draft for Comments |
31 | NIFDC | 2025/7/30 | Test Method for 23 Ingredients Including Procaine in Cosmetics | / | Draft for Comments |
32 | NIFDC | 2025/7/30 | Test Method for 129 Ingredients Including 16α-Hydroxyprednisolone in Cosmetics | / | Draft for Comments |
33 | NMPA | 2025/8/29 | Bovine Corneal Opacity and Permeability Test Method | 2026/3/1 | Newly Added |
34 | NMPA | 2025/8/29 | In Vitro Skin Sensitization: Kinetic Direct Peptide Reactivity Assay Method | 2026/3/1 | Newly Added |
35 | NMPA | 2025/8/29 | In Vitro Skin Absorption Test Method | 2026/3/1 | Newly Added |
36 | NMPA | 2025/8/29 | Immunotoxicity Test Method | 2026/3/1 | Newly Added |
37 | NMPA | 2025/8/29 | Oral Mucosal Irritation Test Method | 2026/3/1 | Newly Added |
38 | NIFDC | 2025/10/14 | 90-Day Oral Toxicity Test Method | / | Draft for Comments |
39 | NIFDC | 2025/10/14 | 90-Day Dermal Toxicity Test Method | / | Draft for Comments |
40 | NIFDC | 2025/10/14 | Bacterial Reverse Mutation Test Method | / | Draft for Comments |
41 | NIFDC | 2025/10/14 | In Vitro Mammalian Cell Chromosomal Aberration Test Method | / | Draft for Comments |
2025 Annual Overview of Cosmetic Ingredient-Related Data Updates
This year, cosmetic ingredient management entered a new phase of dynamic adjustment. The Inventory of Used Cosmetic Ingredients established a tiered management system. Simultaneously, the ingredient usage information database supporting safety assessments was continuously enriched and updated.
Announcement Date | Regulation Content | Effective Date | Status |
2025/2/9 | NIFDC Notice on Updating the "Information on the Use of Ingredients in Marketed Products" | 2025/2/9 | Newly Added |
2025/2/19 | NIFDC's Notice on Publicly Soliciting Comments on "Usage Information for Some Ingredients Included in the International Cosmetic Ingredient Safety Review Data Index (Draft for Comments)" | Before 2025/3/4 | Draft for Comments |
2025/4/10 | NIFDC Notice on Issuing the "Usage Information for Some Ingredients Included in the International Cosmetic Ingredient Safety Review Data Index" | 2025/4/10 | Newly Added |
2025/6/24 | NMPA Announcement on Matters Concerning the Administration of the "Inventory of Used Cosmetic Ingredients" (No. 61, 2025) | 2025/6/24 | Newly Added |
2025/10/20 | NMPA Announces the Inclusion of Three Cosmetic New Ingredients Including Lauroyl Alanine into the "Inventory of Used Cosmetic Ingredients" | 2025/10/20 | Newly Added |
2025/10/31 | NMPA Approves Registration of Two New Cosmetic Ingredients | 2025/10/31 | Newly Added |
In 2025, cosmetic regulation deepened towards more refined and comprehensive oversight. From full-chain safety evaluation to tiered ingredient management, the new regulations encourage enterprises to shift their compliance focus towards 'preventive measures' and the construction of evidence throughout the entire process. Looking ahead to 2026, as regulatory intensity continues to strengthen, only by truly embedding compliance as the cornerstone of their development can companies steadily progress within this environment of deepening regulations and seize new market opportunities.
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