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菲律宾禁止将双酚A(BPA)用作婴儿喂养用品的婴儿奶瓶和吸管杯

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放大字体缩小字体2019-09-26 08:48:20 来源9a href="https://ww2.fda.gov.ph/index.php/issuances-2/cosmetic-laws-and-regulations-pertaining-to-all-regulated-cosmetic-products/cosmetic-fda-circular/612189-fda-circular-no-2019-004-ban-of-bisphenol-a-bpa-from-infant-feeding-bottles-and-sippy-cups-as-child-care-" target="_blank" rel="nofollow">菲律宾食品药品管理局浏览次数9span id="hits">15651
核心提示:法规要求禁止制造、进口和分销含有双酚A(BPA)的婴儿奶瓶和吸管杯;给予所有相关企业六?)个月时间从市场上召回所有含有BPA的婴儿奶瓶和吸管杯;制造商、贸易商、进口商、分销商或批发商有责任对其产品进行召回,以确保将含有双酚A的婴儿奶瓶和吸管杯从市场上撤下,且以后不再出售;违禁产品的制造商、进口商?或分销商应在给定的淘汰期限后一?)个月进行清点并向FDA提交报告;违禁产品的制造商、进口商?或分销商应根据FDA批准的环境和自然资源?环境管理局(DENR-EMB)规则和法规,制定处置计划、/div>
发布单位
菲律宾食品药品管理局
菲律宾食品药品管理局
发布文号 FDA Circular No.2019-004
发布日期 暂无 生效日期 2019-10-09
有效性状?/th> 废止日期 暂无
属?/th> 法规 专业属?/th> 产品及原斘/td>
备注 本法规涵盖作为含BPA的儿童护理产品的婴儿奶瓶和吸管杯以及从事生产、进口、出口、销售、出售、分发、捐赠、转让以及在适用的情况下的用途的场所 测试、促销、广告或赞助包含BPA的任何育儿用品。本法规制定的目的是为了保护儿童健康,尽可能减少接触该物质、/td>
I. RATIONALE

Consistent with the 1987 Philippine Constitution as a declared policy of the State to protect and promote the right to health of the Filipino people and instill health consciousness among them, Republic Act (RA) No. 9711, otherwise known as the Food and Drug Administration (FDA) Act of 2009, and its Implementing Rules and Regulations, the FDA hereby imposes a ban on Bisphenol A (BPA) in infant feeding bottles and sippy cups as child care article products.

II. SCOPE

This Circular shall cover infant feeding bottles and sippy cups as child care article products containing BPA and the establishments that are engaged in the manufacture, importation, exportation, sale, offer for sale, distribution, donation, transfer, and where applicable, the use, testing, promotion, advertising, or sponsorship of any child care articles containing BPA.

III. GENERAL INFORMATION

Bisphenol A (BPA) is an industrial chemical that is widely used as a monomer in the manufacture of polycarbonate (PC); a clear, hard plastic used in many consumer products including feeding bottles and sippy cups. Relevant epidemiological studies have shown that BPA affect the development of the nervous, immune and reproductive system and considered as endocrine disruptors which can alter the hormonal system of the human body. Extensive use of BPA in manufacturing products that come in contact with food increases the risk of exposure to this compound, mainly through the digestive tract.

Over the years, concerns have been raised about BPAs effect on human health, especially when it is used in food contact materials (FCM) and articles such as feeding bottles and sippy cups. In 2008, Canada first proposed the prohibition of polycarbonate baby bottles that contains BPA which came into force in 2010. And in 2011, the European Union (EU) along with China are among the countries which banned the manufacture including the importation of PC baby bottles with BPA.

In the Joint Food and Agriculture Organization and World Health Organization (FAO/WHO) Expert Meeting held on November 2010, the toxicological and health aspects of BPA was reviewed. The expert panels concluded that dietary exposure estimates are generally higher for infants (0-6 months) fed using PC baby bottles with the mean of 2.4 pg/kg body weight per day. This is due to migration of BPA from PC baby bottles when filling the bottle with boiling water, adding milk formula and leaving the bottle to cool down.

Thus, this Circular is issued by the FDA to better protect the health of the children and better reduce exposure to these substances.

IV. POLICIES AND GUIDELINES

  1. The manufacture, importation and distribution of infant feeding bottle and sippy cups containing Bisphenol A (BPA) shall not be allowed.
  2. All concerned establishments shall be given six (6) months phase-out period to recall from the market all infant feeding bottles and sippy cups containing BPA.
  3. It shall be the responsibility of the manufacturer, trader, importer, distributor or wholesaler to conduct recall of their products to ensure that infant feeding bottles and sippy cups containing BPA, are removed from the market and shall no longer be made available to the market after the phase-out period.
  4. The manufacturer, importer and/or distributor of the banned products shall conduct inventory and submit a report to the FDA one (1) month after the given phase-out period.
  5. The manufacturer, importer and/or distributor of the banned products shall prepare a disposal plan in accordance with Department of Environment and Natural Resources- Environmental Management Bureau (DENR-EMB) rules and regulation subject to FDA approval.

V. PENALTY CLAUSE

Any establishment found to be in violation of the provisions of this issuance shall be subjected to sanctions and penalties as prescribed under RA 9711 and its IRR.

VI. EFFECTIVITY

This Circular shall take effect thirty (30) days after publication in two (2) newspapers of general circulation and submission of a copy hereof to the Office of the National Registry of the University of the Philippines Law Center.

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