International Nomenclature of Cosmetic Ingredients (INCI)
A standardized system of ingredient naming developed by the Personal Care Products Council (formerly CTFA), used worldwide for cosmetic ingredient labeling. INCI names are required on product labels in the EU, US, Canada, and most other regulated markets.
The International Nomenclature of Cosmetic Ingredients (INCI) is the internationally recognized naming system for cosmetic ingredients. Originally developed by the Cosmetic, Toiletry, and Fragrance Association (CTFA, now the Personal Care Products Council) in the 1970s, INCI provides a standardized, language-independent way to identify cosmetic ingredients on product labels.
INCI names are assigned based on established chemical nomenclature rules: chemical ingredients typically use modified IUPAC names, botanical ingredients use the Latin binomial (genus and species) followed by the plant part and extract type, and some ingredients retain traditional names (e.g., "Aqua" for water in EU labeling, "Water" in US labeling).
The use of INCI names on cosmetic product labels is mandatory in the EU (Article 19 of EC 1223/2009), the US (21 CFR 701.3), Canada (C.R.C. c.869), and most other regulated markets. Ingredients must be listed in descending order of concentration, with ingredients at concentrations below 1% listed in any order after those above 1%.
The authoritative reference for INCI names is the International Cosmetic Ingredient Dictionary and Handbook, published by the Personal Care Products Council. The EU's CosIng database also provides INCI names for ingredients regulated under EC 1223/2009.
Related Terms
CosIng
The European Commission's official database of cosmetic ingredients (Cosmetic Ingredient database). CosIng contains information on substances and ingredients used in cosmetic products, including INCI names, CAS numbers, restrictions, and references to EC 1223/2009 annexes.
RegulationEU Cosmetics Regulation (EC 1223/2009)
The primary European Union law governing cosmetic products, establishing requirements for safety assessment, CPNP notification, responsible person designation, ingredient restrictions (Annexes II-VI), labeling, and post-market surveillance across all EU/EEA member states.
Regulation21 CFR Part 700
The section of the US Code of Federal Regulations containing FDA regulations specific to cosmetic products, including prohibited ingredients, required warning statements, and labeling requirements. Parts 700-740 collectively govern cosmetics.
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