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In vivo studies of substances used in the cosmetic industry
Cosmetic producers are obliged to guarantee the safety and stability of their products. The current legal regulations are based on the European Union Directive (1223/2009) of 30 November 2009. The main aim of the directive is to formulate criteria of safety of a cosmetic product and requirements tha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969411/ https://www.ncbi.nlm.nih.gov/pubmed/27512349 http://dx.doi.org/10.5114/ada.2016.60607 |
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author | Igielska-Kalwat, Joanna Gościańska, Joanna Witkowska, Beata Nowak, Izabela |
author_facet | Igielska-Kalwat, Joanna Gościańska, Joanna Witkowska, Beata Nowak, Izabela |
author_sort | Igielska-Kalwat, Joanna |
collection | PubMed |
description | Cosmetic producers are obliged to guarantee the safety and stability of their products. The current legal regulations are based on the European Union Directive (1223/2009) of 30 November 2009. The main aim of the directive is to formulate criteria of safety of a cosmetic product and requirements that it must meet to be placed on the market. A new cosmetic product is subjected to thorough investigation prior to its introduction on the market. It should be studied not only with respect to its safety, but also with respect to its effectiveness declared by the producer. The studies are performed in vivo, by the contact or epidermal patch tests on the human skin. |
format | Online Article Text |
id | pubmed-4969411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-49694112016-08-10 In vivo studies of substances used in the cosmetic industry Igielska-Kalwat, Joanna Gościańska, Joanna Witkowska, Beata Nowak, Izabela Postepy Dermatol Alergol Review Paper Cosmetic producers are obliged to guarantee the safety and stability of their products. The current legal regulations are based on the European Union Directive (1223/2009) of 30 November 2009. The main aim of the directive is to formulate criteria of safety of a cosmetic product and requirements that it must meet to be placed on the market. A new cosmetic product is subjected to thorough investigation prior to its introduction on the market. It should be studied not only with respect to its safety, but also with respect to its effectiveness declared by the producer. The studies are performed in vivo, by the contact or epidermal patch tests on the human skin. Termedia Publishing House 2016-06-17 2016-06 /pmc/articles/PMC4969411/ /pubmed/27512349 http://dx.doi.org/10.5114/ada.2016.60607 Text en Copyright © 2016 Termedia Sp. z o.o http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Review Paper Igielska-Kalwat, Joanna Gościańska, Joanna Witkowska, Beata Nowak, Izabela In vivo studies of substances used in the cosmetic industry |
title | In vivo studies of substances used in the cosmetic industry |
title_full | In vivo studies of substances used in the cosmetic industry |
title_fullStr | In vivo studies of substances used in the cosmetic industry |
title_full_unstemmed | In vivo studies of substances used in the cosmetic industry |
title_short | In vivo studies of substances used in the cosmetic industry |
title_sort | in vivo studies of substances used in the cosmetic industry |
topic | Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969411/ https://www.ncbi.nlm.nih.gov/pubmed/27512349 http://dx.doi.org/10.5114/ada.2016.60607 |
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