Cosmetic Labeling : US FDA vs. EU | CosmeReg- eu importing hand sanitizer conply with cosmetics regulation 1223 2009 ,EU Cosmetic Labeling Requirements . EU requires for the cosmetic companies who intend to place a cosmetic product on the EU market to comply with EU cosmetic regulations. Article 19 of the EU cosmetic regulation explains the rules for a compliant cosmetic label. Mandatory information for a cosmetic labelNew EU Cosmetic Regulation Requirements | Microchem LaboratoryAs of July 11, 2013, the previous Cosmetics Directive has been replaced with the new European Union (EU) Cosmetic Regulation 1223/2009. The new regulation's intent is to ensure that the health of consumers' is protected and that EU agencies are well informed of the composition, labeling, and safety of cosmetic and personal care products marketed within the EU.



What Is A Cosmetic Product? | SGS

EU: falls under the scope of cosmetics, as defined in (EC) 1223/2009 Cosmetic Regulation; USA: OTC drug product, with permitted active ingredients for sunscreen function defined in 21 CFR Part 352 (subpart B). This applies whether the product is purely a sunscreen, or has sunscreen as a secondary function

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Europe - Information on Cosmetic Packaging Materials in ...

Information on Cosmetic Packaging Materials in the Context of the EU Cosmetics Regulation EC 1223/2009 This document identifies a set of useful information from packaging/material suppliers that supports the assessment of the impact of the packaging on the safety of the cosmetic product contained therein.

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Europe - Information on Cosmetic Packaging Materials in ...

Information on Cosmetic Packaging Materials in the Context of the EU Cosmetics Regulation EC 1223/2009 This document identifies a set of useful information from packaging/material suppliers that supports the assessment of the impact of the packaging on the safety of the cosmetic product contained therein.

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Hand Sanitiser Regulations - - Explained - - Medic Pro Limited

Typically, a hand sanitiser falls into one or both of the following regulations: Regulation (EC) No 1223/2009 for Cosmetics; Regulation (EU) No 528/2012 for Biocides . How to comply with hand sanitiser regulations . Follow the step by step guide to help you comply with applicable regulations for hand sanitisers: Step 1: Collate information on ...

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Cosmetics and biocides in the EU - The Science Group

1. Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products. 2. Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products. 3. Borderline between Directive 98/8/EC concerning the ...

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EU Regulation 1223/2009 Responsible Person services sell ...

Stringent requirements for Cosmetic companies to sell products in Europe and other countries are being strictly enforced! EU RP-Responsible Person - EU Regulation 1223/2009. EU Regulation 1223/2009, which went into effect July 2013, mandates that all products being sold in the European Union must comply with this regulation.

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EU Regulation 1223/2009 Responsible Person services sell ...

Stringent requirements for Cosmetic companies to sell products in Europe and other countries are being strictly enforced! EU RP-Responsible Person - EU Regulation 1223/2009. EU Regulation 1223/2009, which went into effect July 2013, mandates that all products being sold in the European Union must comply with this regulation.

Get Price

New EU Cosmetic Regulation Requirements | Microchem Laboratory

As of July 11, 2013, the previous Cosmetics Directive has been replaced with the new European Union (EU) Cosmetic Regulation 1223/2009. The new regulation's intent is to ensure that the health of consumers' is protected and that EU agencies are well informed of the composition, labeling, and safety of cosmetic and personal care products marketed within the EU.

Get Price

Is CE Mark required for Hand Sanitizers to be sold in Europe

I had a look into this -and this is definitely a grey area. Disinfectants for the medical field can be considered as an accessory to a medical device and labelled with a CE-mark awarded by a Notified Body in accordance with the Directive 93/42/EEG.

Get Price

New EU Cosmetic Regulation Requirements | Microchem Laboratory

As of July 11, 2013, the previous Cosmetics Directive has been replaced with the new European Union (EU) Cosmetic Regulation 1223/2009. The new regulation's intent is to ensure that the health of consumers' is protected and that EU agencies are well informed of the composition, labeling, and safety of cosmetic and personal care products marketed within the EU.

Get Price

Is CE Mark required for Hand Sanitizers to be sold in Europe

I had a look into this -and this is definitely a grey area. Disinfectants for the medical field can be considered as an accessory to a medical device and labelled with a CE-mark awarded by a Notified Body in accordance with the Directive 93/42/EEG.

Get Price

EU Regulation 1223/2009 Responsible Person services sell ...

Stringent requirements for Cosmetic companies to sell products in Europe and other countries are being strictly enforced! EU RP-Responsible Person - EU Regulation 1223/2009. EU Regulation 1223/2009, which went into effect July 2013, mandates that all products being sold in the European Union must comply with this regulation.

Get Price

New EU Cosmetic Regulation Requirements | Microchem Laboratory

As of July 11, 2013, the previous Cosmetics Directive has been replaced with the new European Union (EU) Cosmetic Regulation 1223/2009. The new regulation's intent is to ensure that the health of consumers' is protected and that EU agencies are well informed of the composition, labeling, and safety of cosmetic and personal care products marketed within the EU.

Get Price

Hand Sanitiser Regulations - - Explained - - Medic Pro Limited

Typically, a hand sanitiser falls into one or both of the following regulations: Regulation (EC) No 1223/2009 for Cosmetics; Regulation (EU) No 528/2012 for Biocides . How to comply with hand sanitiser regulations . Follow the step by step guide to help you comply with applicable regulations for hand sanitisers: Step 1: Collate information on ...

Get Price

Is CE Mark required for Hand Sanitizers to be sold in Europe

I had a look into this -and this is definitely a grey area. Disinfectants for the medical field can be considered as an accessory to a medical device and labelled with a CE-mark awarded by a Notified Body in accordance with the Directive 93/42/EEG.

Get Price

EU Regulation 1223/2009 Responsible Person services sell ...

Stringent requirements for Cosmetic companies to sell products in Europe and other countries are being strictly enforced! EU RP-Responsible Person - EU Regulation 1223/2009. EU Regulation 1223/2009, which went into effect July 2013, mandates that all products being sold in the European Union must comply with this regulation.

Get Price

Europe - Information on Cosmetic Packaging Materials in ...

Information on Cosmetic Packaging Materials in the Context of the EU Cosmetics Regulation EC 1223/2009 This document identifies a set of useful information from packaging/material suppliers that supports the assessment of the impact of the packaging on the safety of the cosmetic product contained therein.

Get Price

Cosmetic Labeling : US FDA vs. EU | CosmeReg

EU Cosmetic Labeling Requirements . EU requires for the cosmetic companies who intend to place a cosmetic product on the EU market to comply with EU cosmetic regulations. Article 19 of the EU cosmetic regulation explains the rules for a compliant cosmetic label. Mandatory information for a cosmetic label

Get Price

Is CE Mark required for Hand Sanitizers to be sold in Europe

I had a look into this -and this is definitely a grey area. Disinfectants for the medical field can be considered as an accessory to a medical device and labelled with a CE-mark awarded by a Notified Body in accordance with the Directive 93/42/EEG.

Get Price

Cosmetics and biocides in the EU - The Science Group

1. Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products. 2. Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products. 3. Borderline between Directive 98/8/EC concerning the ...

Get Price

Cosmetic Labeling : US FDA vs. EU | CosmeReg

EU Cosmetic Labeling Requirements . EU requires for the cosmetic companies who intend to place a cosmetic product on the EU market to comply with EU cosmetic regulations. Article 19 of the EU cosmetic regulation explains the rules for a compliant cosmetic label. Mandatory information for a cosmetic label

Get Price

Cosmetics and biocides in the EU - The Science Group

1. Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products. 2. Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products. 3. Borderline between Directive 98/8/EC concerning the ...

Get Price

What Is A Cosmetic Product? | SGS

EU: falls under the scope of cosmetics, as defined in (EC) 1223/2009 Cosmetic Regulation; USA: OTC drug product, with permitted active ingredients for sunscreen function defined in 21 CFR Part 352 (subpart B). This applies whether the product is purely a sunscreen, or has sunscreen as a secondary function

Get Price

What Is A Cosmetic Product? | SGS

EU: falls under the scope of cosmetics, as defined in (EC) 1223/2009 Cosmetic Regulation; USA: OTC drug product, with permitted active ingredients for sunscreen function defined in 21 CFR Part 352 (subpart B). This applies whether the product is purely a sunscreen, or has sunscreen as a secondary function

Get Price