{"id":252,"date":"2024-01-15T20:49:31","date_gmt":"2024-01-15T20:49:31","guid":{"rendered":"https:\/\/www.libertymanagement.us\/fda-support\/?p=252"},"modified":"2024-01-15T20:49:31","modified_gmt":"2024-01-15T20:49:31","slug":"cosmetic-facility-registration","status":"publish","type":"post","link":"https:\/\/www.libertymanagement.us\/fda-support\/2024\/01\/15\/cosmetic-facility-registration\/","title":{"rendered":"COSMETIC FACILITY REGISTRATION"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">As per MoCRA, owner or operator of a facility that\nmanufactures or processes <a href=\"https:\/\/www.fdahelp.us\/cosmetics.html\">cosmetic\nproducts<\/a> for US distribution must <a href=\"https:\/\/www.libertymanagement.us\/cosmetic-facility-registration\/\">register\nwith FDA<\/a>, whether the facility is located in the US or abroad. Registration\nrequires certain information to be provided to FDA, such as all brand names\nunder which the cosmetic products are manufactured or processed in the facility\nare sold, the product category or categories, and the responsible person for\neach cosmetic product manufactured or processed at the facility. A responsible\nperson is the manufacturer, packer, or distributor of a cosmetic product whose\nname appears on the label.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">A manufacturing facility needs to submit only one <a href=\"https:\/\/www.fdahelp.us\/fda-cosmetic-registration.html\">facility\nregistration<\/a> regardless of whether that facility manufactures or produces\ncosmetic products for themselves or on behalf of multiple responsible persons.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">This requirement excludes certain beauty shops, salons, and\nretailers and establishments that only perform labeling, relabeling, packaging,\nrepackaging, holding, and distributing of cosmetic products.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Facilities that manufactured or processed cosmetic products\non or before December 29, 2022, must register by July 1<sup>st<\/sup>, 2024.\nFacilities that engaged in manufacturing or processing after December 2022 must\nregister within 60 days of first engaging in such activity or by July 1<sup>st<\/sup>,\n2024, whichever is later. <\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Facilities registrations must be renewed biennially.\nRegistration must be updated with new information within 60 days of such a\nchange.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">FDA has launched new submission portal to facilitate\nregistration.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/www.fdahelp.us\/\">Liberty Management Group\nLtd.<\/a> can help you with registration under FDA MoCRA regulations. <\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><em>Namrata <\/em><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><em>Regulatory Consultant<\/em><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><em>support@libertymanagement.us<\/em><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"http:\/\/www.fdahelp.us\">http:\/\/www.fdahelp.us<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>As per MoCRA, owner or operator of a facility that manufactures or processes cosmetic products for US distribution must register with FDA, whether the facility is located in the US or abroad. Registration requires certain information to be provided to FDA, such as all brand names under which the cosmetic products are manufactured or processed &hellip; <a href=\"https:\/\/www.libertymanagement.us\/fda-support\/2024\/01\/15\/cosmetic-facility-registration\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;COSMETIC FACILITY REGISTRATION&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[10,70,64],"class_list":["post-252","post","type-post","status-publish","format-standard","hentry","category-cosmetics-regulations","tag-cosmetic-registration","tag-mocra","tag-register-with-fda"],"_links":{"self":[{"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/posts\/252","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/comments?post=252"}],"version-history":[{"count":1,"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/posts\/252\/revisions"}],"predecessor-version":[{"id":253,"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/posts\/252\/revisions\/253"}],"wp:attachment":[{"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/media?parent=252"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/categories?post=252"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.libertymanagement.us\/fda-support\/wp-json\/wp\/v2\/tags?post=252"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}