Retained EU Law 2009 United Kingdom

Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products (recast) (Text with EEA relevance)

At a glance

What's here

5 compliance obligations

What this Act requires

Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.

s.art004

Responsible person

  • Ensure a responsible person is in place before selling cosmetic products
s.art006

Obligations of distributors

  • Distributors: check cosmetic products before placing on market
s.art007

Identification within the supply chain

  • Supply chain identification for cosmetic products
s.art008

Good manufacturing practice

  • Manufacture cosmetic products in line with good manufacturing practice
s.art023

Communication of serious undesirable effects

  • Report serious cosmetic product side effects to authorities immediately
Browse 38 other sections — procedural / definitional / commencement
s.annex 2 para.1

For the purposes of the Annexes II to VI: ‘Rinse-off...

s.annex viii para.1

This Annex lists the alternative methods validated by the European...

s.art001

Scope and objective

s.art002

Definitions

s.art003

Safety

s.art005

Obligations of responsible persons

s.art005

Obligations of responsible persons established in Northern Ireland

s.art009

Free movement

s.art010

Safety assessment

s.art011

Product information file

s.art012

Sampling and analysis

s.art013

Notification

s.art014

Restrictions for substances listed in the Annexes

s.art015

Substances classified as CMR substances

s.art016

Nanomaterials

s.art017

Traces of prohibited substances

s.art018

Animal testing

s.art019

Labelling

s.art020

Product claims

s.art021

Access to information for the public

s.art022

In-market control

s.art024

Information on substances

s.art025

Non-compliance by the responsible person

s.art026

Non-compliance by distributors

s.art027

Safeguard clause

s.art028

Good administrative practices

s.art029

Cooperation between competent authorities

s.art030

Power to amend Articles

s.art031

Power to amend the annexes

s.art032

Procedure for making regulations

s.art033

Further duties of the Secretary of State

s.art034

Competent authorities, poison control centres or assimilated entities

s.art035

Annual report on animal testing

s.art036

Formal objection against harmonised standards

s.art037

Penalties

s.art038

Repeal

s.art039

Transitional provisions

s.art040

Entry into force and date of application

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