{"id":427,"date":"2026-06-04T09:59:06","date_gmt":"2026-06-04T01:59:06","guid":{"rendered":"https:\/\/www.wanbonet.com.cn\/274_apexcs\/?p=427"},"modified":"2026-07-24T13:45:15","modified_gmt":"2026-07-24T05:45:15","slug":"fda-registration-basics-for-food-facilities","status":"publish","type":"post","link":"https:\/\/www.wanbonet.com.cn\/274_apexcs\/resources\/fda-registration-basics-for-food-facilities\/","title":{"rendered":"U.S. Cosmetic Compliance After MoCRA"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"427\" class=\"elementor elementor-427\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-59d64f50 e-con-full e-flex e-con e-parent\" data-id=\"59d64f50\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-22898f66 e-con-full e-flex e-con e-child\" data-id=\"22898f66\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-2704245e elementor-widget elementor-widget-text-editor\" data-id=\"2704245e\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>The Modernization of Cosmetics Regulation Act of 2022 expanded federal requirements for cosmetic businesses. Depending on the company\u2019s role and available exemptions, cosmetic facilities may need FDA registration and responsible persons may need to list marketed cosmetic products.<\/p><p>\u00a0<\/p><p>Cosmetic companies should maintain adequate safety substantiation, report serious adverse events, keep required records, and ensure the product is not adulterated or misbranded. Product identity and intended use matter: claims that treat disease or affect body structure or function may cause a cosmetic to be regulated as a drug.<\/p><p>\u00a0<\/p><p>Imported cosmetics are subject to FDA review at entry and must meet the same legal standards as domestic products. The importer should verify ingredient restrictions, color additive requirements, English labeling, net quantity, business identification, warning statements, and claim language.<\/p><p>\u00a0<\/p><p>Because cosmetic rules and implementation guidance continue to evolve, businesses should periodically reassess registration, listing, labeling, and recordkeeping obligations rather than relying on a one-time review.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-21adfc0 e-con-full e-flex e-con e-child\" data-id=\"21adfc0\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t<div class=\"elementor-element elementor-element-59707a03 elementor-widget elementor-widget-text-editor\" data-id=\"59707a03\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><strong>APEX CS practical takeaway: <\/strong>Confirm the product-specific regulatory pathway before production, testing, labeling, or shipment. Requirements vary by device design, intended use, claims, market channel, and final configuration.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Understand facility registration, product listing, safety substantiation, adverse-event, and labeling considerations.<\/p>\n","protected":false},"author":1,"featured_media":361,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center 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center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[27,31],"tags":[],"class_list":["post-427","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-resources","category-fda-compliance-updates"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>U.S. Cosmetic Compliance After MoCRA - APEX Compliance &amp; Supply LLC<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.wanbonet.com.cn\/274_apexcs\/resources\/fda-registration-basics-for-food-facilities\/\" \/>\n<meta property=\"og:locale\" content=\"zh_CN\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta 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