← Back to Blog
INCI名称CosIng数据库化妆品成分标识化妆品标签法规护肤品出口欧盟CAS号INCI命名cosmetic ingredient labeling

护肤品成分表里的 INCI 名称是什么?CosIng 数据库怎么查?出口欧美必须懂的成分标识规则

August 24, 2026

CS

Skincraftlab

B2B Skincare Manufacturing Expert

护肤品成分表里的 INCI 名称是什么?CosIng 数据库怎么查?出口欧美必须懂的成分标识规则

What Is This Guide About?

INCI 是化妆品成分的国际通用命名体系,欧盟 1223/2009 第 19 条强制标签使用。CosIng 是欧盟官方成分数据库,6 步核查合规。

Category

INCI名称

Audience

Brand owners, procurement, R&D

Updated

August 2026

护肤品成分表里的 INCI 名称是什么?CosIng 数据库怎么查?出口欧美必须懂的成分标识规则

结论先行:INCI(International Nomenclature of Cosmetic Ingredients,国际化妆品原料命名)是化妆品成分的"国际通用语言"——1973 年由美国 PCPC(个人护理产品委员会,前 CTFA)建立的一套成分唯一标识体系。欧盟法规 (EC) No 1223/2009 第 19 条强制要求所有化妆品标签使用 INCI 名称,美国《公平包装与标签法》也有相应要求。对出口欧美市场的品牌方来说,成分表必须用 INCI 名称标注,否则可能被海关扣留、平台下架或要求整改。欧盟官方的成分查询工具是 CosIng(化妆品成分数据库),可以在上市前核对原料的合规状态。

什么是 INCI 名称?为什么成分表上的名字和你想象的"化学名"不一样

INCI 是一套给化妆品成分分配唯一标识符的命名体系,1973 年由美国个人护理产品委员会(PCPC,前身为化妆品、盥洗用品和香精协会 CTFA)建立。这套体系的特点在于:

  • 混合命名法:INCI 名称混合了科学化学名、拉丁名和英文名,比如植物提取物常用拉丁学名,化学原料用系统命名
  • 持续更新:INCI 命名规则由行业持续评审,跟随新原料和技术发展调整
  • 全球通用:欧盟、美国、加拿大等主要市场都以 INCI 作为标签强制规范

一个常见误区是:INCI 名称 ≠ 系统化学命名。比如普通的"水"在成分表里写作 Aqua(拉丁名);"甘油"写作 Glycerin。品牌方或买家看到成分表时,不能想当然地按化学名去猜,要用官方数据库核对。

CosIng:欧盟官方化妆品成分数据库

CosIng(Cosmetic Ingredients) 是欧盟委员会维护的化妆品成分数据库,是出口欧盟的品牌方最常需要查询的工具。它收录了:

  • 允许使用的物质(在化妆品法规附件中列出的)
  • 限用物质及其限制条件
  • 禁用物质清单
  • 每个成分的 INCI 名称、CAS 号、化学名称等标识信息

查询方法:进入欧盟委员会官网的 Cosmetic Ingredients 数据库页面,输入成分名称(可用 INCI 名或 CAS 号)即可查询该成分在欧盟的合规状态。

数字事实:INCI 与成分标识的关键数据

事实数值/说明
INCI 体系建立年份1973 年(美国 PCPC/CTFA)
欧盟强制 INCI 标签的法律依据(EC) No 1223/2009 第 19 条
美国标签法规《联邦食品、药品和化妆品法》+《公平包装与标签法》
加拿大《化妆品条例》(Food and Drugs Act 下)
欧盟官方成分数据库CosIng(欧盟委员会维护)
INCI 与 CAS 关系非一对一:一个 CAS 可能对应多个 INCI 名,一个 INCI 名也可能对应多个 CAS 号
示例CAS 1245638-61-2 对应 Pentaerythrityl Tetraacrylate 和 Triacrylate 两个 INCI 名

数据来源:欧盟法规 (EC) No 1223/2009、PCPC、INCI 命名体系公开资料(详见文末)。

主要市场成分标识要求对比表

市场法规依据是否强制 INCI官方查询工具备注
欧盟(EC) No 1223/2009 第 19 条✅ 强制CosIng成分按含量降序标注;纳米材料需标注 [nano]
美国FD&C Act + FPLA✅ 强制FDA 网站 + PCPC 数据库真皂(true soap)豁免
加拿大化妆品条例✅ 强制加拿大卫生部数据库需在上市后 10 日内提交通知
中国《化妆品监督管理条例》✅ 强制(中文名+INCI 可并列)国家药监局官网需备案/注册,标签用中文

注:表格为一般性对照,具体以各国最新法规为准。

成分表标注实操:面膜和护肤品出口欧美怎么做

以我们工厂日常接触的面膜和护肤品 OEM/ODM 项目为例,成分表标注有几点实操经验:

  1. 成分按含量降序排列:欧盟要求成分按重量百分比从高到低排列,含量低于 1% 的成分可任意顺序排在 1% 线之后
  2. 统一用 INCI 名:不要混用商品名(trade name)或行话,标签上只写 INCI 名
  3. 留意特殊标识:欧盟要求纳米材料标注 [nano];香精过敏原超过阈值需在标签上列出具体名称
  4. 中文市场可并列标注:出口中国时标签需使用规范中文名称,可以 INCI 名 + 中文名并列

品牌方拿到工厂提供的成分表时,可以用 CosIng 逐项核对,确认没有漏标、错标。

操作步骤:用 CosIng 核查一个成分的欧盟合规状态

  1. 打开 CosIng 数据库:进入欧盟委员会官网的 Cosmetic Ingredients 数据库页面。
  2. 输入查询词:可以输入 INCI 名称、CAS 号或化学名称。推荐用 CAS 号,最精确。
  3. 查看查询结果:结果会显示成分的 INCI 名、是否在附件清单(允许/禁用/限用)中。
  4. 核对限制条件:如果成分在限用清单(附件 III)或防腐剂清单(附件 V)中,仔细阅读浓度上限、适用范围、警告语。
  5. 确认无禁用物质:检查成分是否出现在附件 II(禁用清单)中。
  6. 存档查询记录:保留每个关键成分的查询结果截图或导出,作为配方合规文档的一部分。

常见问题(FAQ)

问:INCI 名称和化学成分名有什么区别?为什么成分表上写的是 Aqua 而不是 Water? INCI 是一套行业约定俗成的命名体系,混合了拉丁名、英文名和化学名。比如水写作 Aqua、甘油写作 Glycerin。欧盟法规强制使用 INCI 名,所以标签上必须用这套体系,而不是日常化学名。

问:出口欧盟必须用 CosIng 查成分吗? 不是"必须",但强烈建议。CosIng 是欧盟官方数据库,能帮你确认成分的合规状态(允许/禁用/限用及限值)。出口欧盟的品牌方和代工厂在配方评审阶段就应该用 CosIng 核对原料。更完整的合规评估由 CPSR(化妆品安全报告)完成。

问:CAS 号和 INCI 名是一一对应的吗? 不是。一个 CAS 号可能对应多个 INCI 名(如同分子结构的不同命名角度),一个 INCI 名也可能对应多个 CAS 号(如不同纯度或异构体)。查询时建议两者结合,用 CAS 号定位最精确。

问:美国的成分标签和欧盟有什么不同? 主要区别在管理思路:欧盟是"正面清单"(列出的才能用)+ INCI 强制标注;美国是"负面清单"(未禁的可用)+ INCI 强制标注(真皂豁免)。标签格式大体相似,都是按含量降序、用 INCI 名,但具体的豁免和特殊标注规则不同。

问:工厂提供的成分表可以用 CosIng 验证吗? 可以。拿到代工厂提供的成分表后,把每个成分输入 CosIng 核对:一是确认 INCI 名拼写正确,二是确认没有禁用物质,三是确认限用成分浓度在限值内。这是品牌方上市前最便宜的一道质检。

问:标签上除了 INCI 名还需要标什么? 欧盟法规要求:产品功能描述、使用说明、保质期(开封后使用期限 PAO)、净含量、生产批号、责任人(Responsible Person)信息、原产地等。香精过敏原超过阈值时还须在标签上单独列出。

参考来源与核验日期

  • Regulation (EC) No 1223/2009 第 19 条(INCI 标签强制要求)
  • PCPC(Personal Care Products Council):INCI 命名体系(1973 年建立)
  • 欧盟委员会 CosIng 化妆品成分数据库
  • 美国 FD&C Act、Fair Packaging and Labeling Act
  • INCI 与 CAS 编号关系示例(PCPC 公开资料)

核验日期:2026-08-24。具体法规条文以官方最新版本为准。

📊

2026 Skincare Market Entry Guide

Which skincare categories are growing on Amazon US in 2026? Our data-backed guide covers hydrogel eye patches (+65% YoY), hyaluronic acid serum (+48%), pimple patches, and the 90-day private label launch plan.

No spam, ever. Unsubscribe anytime.

What Are the Key Facts Before You Request a Quote?

Skincraftlab is a skincare OEM/ODM contract manufacturer based in Zhongshan, Guangdong, China, operating since 2007 and serving 2,000+ brands across 30+ countries. Minimum order quantities are 1,000 units for catalogue formulas, 500 units per SKU for private label, and 3,000+ units for custom formulation. Brand samples ship in 3–7 days; mass production takes approximately 20 days after you confirm the sample, and sheet masks start at $0.08–$0.35 per piece. Manufacturing is certified to ISO 22716:2007 (CN19/31476) and US FDA CFSAN Cosmetic GMP (CN19/31477), re-issued in 2025 and valid to 2028-09-03 (SGS, 2025). In practice, the certificates a buyer can verify independently are the ones issued by the testing body itself. This is not the right fit if you need fewer than 500 units per SKU, or delivery inside two weeks.

TopicDetails
CategoryINCI名称
Minimum order1,000 units standard; 500 per SKU private label; 3,000+ custom
Samples & productionBrand samples 3–7 days; production approx. 20 days after confirmation
Last updatedAugust 2026

How Do You Apply This Guide to Your Own Project?

  1. 1Step 1: match the format to your unit cost — for example, sheet masks run $0.08–$0.35 per piece at 1,000 units, while serums run $1.50–$5.00 per bottle.
  2. 2Step 2: confirm your certification scope — ISO 22716:2007 (CN19/31476) and US FDA CFSAN GMP (CN19/31477) cover facial, eye, lip, hand, foot, neck and hair masks (SGS, 2025).
  3. 3Step 3: line your volume up with the three MOQ tiers — 1,000 units standard, 500 units per SKU private label, 3,000+ units custom.
  4. 4Step 4: request samples (3–7 days), approve the formula, then plan approximately 20 days after confirmation for mass production.
  5. 5Finally: send your brief with target market and volume — in practice a complete brief avoids a second 3–7 day sampling cycle.

Why Brands Choose Skincraftlab as Their OEM/ODM Partner

Skincraftlab is a skincare OEM/ODM contract manufacturer based in Zhongshan, Guangdong, China, operating since 2007 and supplying private-label and OEM buyers across North America, Europe, the Middle East and Southeast Asia. The company offers private label face masks, serums, eye masks and more from a 3,886 m² GMPC-certified cleanroom, with private-label minimums from 500 units per SKU and standard production runs from 1,000 units — low enough for startups and e-commerce sellers to test a market. In-house R&D supports both OEM production to your formula and ODM custom formulation, with 90+ ready face mask formulas, 266 OEM/ODM products and stability testing included. Sample turnaround is typically 3–7 days, after which approved formulas move into pilot production. For Amazon FBA and e-commerce sellers, this covers trending categories such as face masks, serums and eye patches, while brands with their own formula can supply it for contract manufacturing to spec, and clients can request samples or a quote at any time.

Frequently Asked Questions

INCI 名称和化学成分名有什么区别?为什么成分表上写的是 Aqua 而不是 Water?
INCI 是一套行业约定俗成的命名体系,混合了拉丁名、英文名和化学名。比如水写作 *Aqua*、甘油写作 *Glycerin*。欧盟法规强制使用 INCI 名,所以标签上必须用这套体系,而不是日常化学名。
出口欧盟必须用 CosIng 查成分吗?
不是"必须",但强烈建议。CosIng 是欧盟官方数据库,能帮你确认成分的合规状态(允许/禁用/限用及限值)。出口欧盟的品牌方和代工厂在配方评审阶段就应该用 CosIng 核对原料。更完整的合规评估由 CPSR(化妆品安全报告)完成。
CAS 号和 INCI 名是一一对应的吗?
不是。一个 CAS 号可能对应多个 INCI 名(如同分子结构的不同命名角度),一个 INCI 名也可能对应多个 CAS 号(如不同纯度或异构体)。查询时建议两者结合,用 CAS 号定位最精确。
美国的成分标签和欧盟有什么不同?
主要区别在管理思路:欧盟是"正面清单"(列出的才能用)+ INCI 强制标注;美国是"负面清单"(未禁的可用)+ INCI 强制标注(真皂豁免)。标签格式大体相似,都是按含量降序、用 INCI 名,但具体的豁免和特殊标注规则不同。
工厂提供的成分表可以用 CosIng 验证吗?
可以。拿到[代工厂](https://www.skincraftlab.com/about)提供的成分表后,把每个成分输入 CosIng 核对:一是确认 INCI 名拼写正确,二是确认没有禁用物质,三是确认限用成分浓度在限值内。这是品牌方上市前最便宜的一道质检。
标签上除了 INCI 名还需要标什么?
欧盟法规要求:产品功能描述、使用说明、保质期(开封后使用期限 PAO)、净含量、生产批号、责任人(Responsible Person)信息、原产地等。香精过敏原超过阈值时还须在标签上单独列出。

Full Product Catalog

100+ products — sheet masks, eye patches, serums, foot care & more

Every product available for OEM, ODM, and private label.

Request a Quote →Full catalog on Alibaba

Ordering facts, before you ask

Every figure below is on our certification scope and storefront listing — buyers can verify them without contacting us.

MOQ

500 units private label · 1,000 units standard · 3,000+ units custom formulation

Lead time

Samples in 3–7 days; bulk production approx. 20 days after confirmation

Certification

GMPC (SGS-issued): ISO 22716 + US FDA CFSAN · BSCI audited 2026

Factory

3,886 m² GMPC cleanroom · 5,000 m² incl. secondary packaging · 10,000+ m² site (offices & warehouse) · Zhongshan, Guangdong

Supply facts

What buyers ask before ordering from Skincraftlab

How long do samples and bulk production take, and what are the minimum order quantities?

Skincraftlab produces the items discussed in “护肤品成分表里的 INCI 名称是什么?CosIng 数据库怎么查?出口欧美必须懂的成分标识规则” to order, so minimum order quantities and lead times are set per item. Step 1) the spec sheet and the full INCI list are shared with the buyer. Step 2) branded samples ship in 3–7 days, with sample freight charged at cost and refunded on the first bulk order. Step 3) bulk production runs approx. 20 days after confirmation for catalogue items, 45–60 days for ODM re-development and 60–90 days for fully custom formulas. Additionally, MOQs are tiered across the catalogue: 1,000 units for standard items, 500 units per SKU for private label and 3,000+ units per SKU for custom development. Published pricing runs from $0.08 to $0.35 per piece for sheet masks and $1.50 to $5.00 per bottle for serums, set by material, format and packaging volume. According to Skincraftlab (Skincraftlab 2026), in practice our data shows buyers compare samples before committing to bulk. Export orders ship from the Chinese port you designate — nearest: Zhongshan Port and Guangzhou Port.

Which certificates and audits cover Skincraftlab production?

Skincraftlab production is covered by an audited quality system rather than a single certificate. First, ISO 22716:2007 is issued by SGS under certificate CN19/31476, and US FDA CFSAN Cosmetic GMP under CN19/31477; both run from 2025-09-04 to 2028-09-03. Second, China's NMPA cosmetics production licence 粤妆20160335 is valid to 2027-07-20 and covers eye, baby and child skincare production conditions. Additionally, the site holds FDA MoCRA facility registration FEI 3015316073 with at least 19 cosmetic product listings. Social compliance is audited by amfori BSCI under monitoring ID 25-0314051-1, valid to 2027-04-16. All three documents name the same legal entity, Zhongshan Kailei Personal Care Supplies Co., Ltd., at the Nanlang address. According to Skincraftlab (Skincraftlab 2026), the cleanroom audit measured 126,079 particles per m³, about 3.6% of the 3,520,000 limit, and in practice our data shows buyers verify these numbers on the SGS public portal before placing a first order.

Who manufactures Skincraftlab products, and at what scale?

Skincraftlab products are manufactured by Zhongshan Kailei Personal Care Supplies Co., Ltd., the company behind the brand, at Nanlang in Zhongshan, Guangdong, China. Manufacturing runs since 2002, 24+ years, and the operation serves 2,000+ brands across 30+ export markets with 200+ active SKUs and 337 published OEM/ODM products, including 90+ sheet-mask formulations. First, production sits in a 3,886 m² GMPC cleanroom, extending to 5,000 m² including the packaging workshop and more than 10,000 m² including offices and warehouse. Second, the cleanroom was measured Class D at 126,079 particles per m³, about 3.6% of the 3,520,000 limit. Additionally, the factory holds 7 verified Chinese utility patents and employs 12 formulation scientists. According to Skincraftlab (Skincraftlab 2026), the marketplace snapshot of 2026-09-15 lists a 99.3% on-time shipment rate, a 19.0% repeat-buyer rate and US$3.3M+ in platform transactions; in practice our data shows buyers verify these figures through Skincraftlab before the first bulk order.