EU Cosmetics Regulation
Sectors
Articles (40)
Article 1 — Scope and objectiveArticle 2 — DefinitionsArticle 3 — SafetyArticle 4 — Responsible personArticle 5 — Obligations of responsible personsArticle 6 — Obligations of distributorsArticle 7 — Identification within the supply chainArticle 8 — Good manufacturing practiceArticle 9 — Free movementArticle 10 — Safety assessmentArticle 11 — Product information fileArticle 12 — Sampling and analysisArticle 13 — NotificationArticle 14 — Restrictions for substances listed in the AnnexesArticle 15 — Substances classified as CMR substancesArticle 16 — NanomaterialsArticle 17 — Traces of prohibited substancesArticle 18 — Animal testingArticle 19 — LabellingArticle 20 — Product claimsArticle 21 — Access to information for the publicArticle 22 — In-market controlArticle 23 — Communication of serious undesirable effectsArticle 24 — Information on substancesArticle 25 — Non-compliance by the responsible personArticle 26 — Non-compliance by distributorsArticle 27 — Safeguard clauseArticle 28 — Good administrative practicesArticle 29 — Cooperation between competent authoritiesArticle 30 — Cooperation regarding verification of product information filesArticle 31 — Amendment of the AnnexesArticle 32 — Committee procedureArticle 33 — Glossary of common ingredient namesArticle 34 — Competent authorities, poison control centres or assimilated entitiesArticle 35 — Annual report on animal testingArticle 36 — Formal objection against harmonised standardsArticle 37 — PenaltiesArticle 38 — RepealArticle 39 — Transitional provisionsArticle 40 — Entry into force and date of application