Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 ... (32009R1223)
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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)
- 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)
- CHAPTER I
- SCOPE, DEFINITIONS
- Article 1
- Scope and objective
- Article 2
- Definitions
- CHAPTER II
- SAFETY, RESPONSIBILITY, FREE MOVEMENT
- Article 3
- Safety
- Article 4
- Responsible person
- Article 5
- Obligations of responsible persons
- Article 6
- Obligations of distributors
- Article 7
- Identification within the supply chain
- Article 8
- Good manufacturing practice
- Article 9
- Free movement
- CHAPTER III
- SAFETY ASSESSMENT, PRODUCT INFORMATION FILE, NOTIFICATION
- Article 10
- Safety assessment
- Article 11
- Product information file
- Article 12
- Sampling and analysis
- Article 13
- Notification
- CHAPTER IV
- RESTRICTIONS FOR CERTAIN SUBSTANCES
- Article 14
- Restrictions for substances listed in the Annexes
- Article 15
- Substances classified as CMR substances
- Article 16
- Nanomaterials
- Article 17
- Traces of prohibited substances
- CHAPTER V
- ANIMAL TESTING
- Article 18
- Animal testing
- CHAPTER VI
- CONSUMER INFORMATION
- Article 19
- Labelling
- Article 20
- Product claims
- Article 21
- Access to information for the public
- CHAPTER VII
- MARKET SURVEILLANCE
- Article 22
- In-market control
- Article 23
- Communication of serious undesirable effects
- Article 24
- Information on substances
- CHAPTER VIII
- NON-COMPLIANCE, SAFEGUARD CLAUSE
- Article 25
- Non-compliance by the responsible person
- Article 26
- Non-compliance by distributors
- Article 27
- Safeguard clause
- Article 28
- Good administrative practices
- CHAPTER IX
- ADMINISTRATIVE COOPERATION
- Article 29
- Cooperation between competent authorities
- Article 30
- Cooperation regarding verification of product information files
- CHAPTER X
- IMPLEMENTING MEASURES, FINAL PROVISIONS
- Article 31
- Amendment of the Annexes
- Article 32
- Committee procedure
- Article 33
- Glossary of common ingredient names
- Article 34
- Competent authorities, poison control centres or assimilated entities
- Article 35
- Annual report on animal testing
- Article 36
- Formal objection against harmonised standards
- Article 37
- Penalties
- Article 38
- Repeal
- Article 39
- Transitional provisions
- Article 40
- Entry into force and date of application
- ANNEX I
- COSMETIC PRODUCT SAFETY REPORT
- PART A – Cosmetic product safety information
- 1. Quantitative and qualitative composition of the cosmetic product
- 2. Physical/chemical characteristics and stability of the cosmetic product
- 3. Microbiological quality
- 4. Impurities, traces, information about the packaging material
- 5. Normal and reasonably foreseeable use
- 6. Exposure to the cosmetic product
- 7. Exposure to the substances
- 8. Toxicological profile of the substances
- 9. Undesirable effects and serious undesirable effects
- 10. Information on the cosmetic product
- PART B – Cosmetic product safety assessment
- 1. Assessment conclusion
- 2. Labelled warnings and instructions of use
- 3. Reasoning
- 4. Assessor's credentials and approval of part B
- Preamble to Annexes II to VI
- ANNEX II
- LIST OF SUBSTANCES PROHIBITED IN COSMETIC PRODUCTS
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