{"id":34567,"date":"2025-06-06T12:00:02","date_gmt":"2025-06-06T16:00:02","guid":{"rendered":"https:\/\/advisory.avalerehealth.com\/?p=34567"},"modified":"2025-06-20T17:53:08","modified_gmt":"2025-06-20T21:53:08","slug":"acnu-provides-a-new-fda-approval-pathway-for-prescription-to-otc-drugs","status":"publish","type":"post","link":"https:\/\/advisory.avalerehealth.com\/insights\/acnu-provides-a-new-fda-approval-pathway-for-prescription-to-otc-drugs","title":{"rendered":"ACNU Provides a New FDA Approval Pathway for Prescription-to-OTC Drugs"},"content":{"rendered":"<p><b><span data-contrast=\"auto\">Previous FDA Policy Delineating Prescription and OTC Status<\/span><\/b><span data-ccp-props=\"{}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">Prior to the Additional Condition for Non-prescription Use (ACNU) final rule, FDA regulations only allowed prescription (Rx) drug products to be either fully (\u201cfull Rx-to-over-the-counter [OTC] switch\u201d) or partially (\u201cpartial Rx-to-OTC switch\u201d; e.g., only specific strengths or indications) changed to non-prescription marketing status. This meant that a single product could not be simultaneously designated as a prescription and non-prescription product for all use cases.\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">To switch a product to non-prescription status, sponsors would have had to demonstrate that the drug product was both efficacious and safe to use in a non-prescription setting and that the label contained sufficient information for consumers to use the drug safely and effectively without a healthcare professional\u2019s supervision. The FDA provided guidance documents on <\/span><a href=\"https:\/\/www.fda.gov\/media\/75626\/download?attachment\"><span data-contrast=\"none\">label comprehension studies<\/span><\/a><span data-contrast=\"auto\"> and <\/span><a href=\"https:\/\/www.fda.gov\/files\/drugs\/published\/Self-Selection-Studies-for-Nonprescription-Drug-Products.pdf\"><span data-contrast=\"none\">self-selection studies<\/span><\/a><span data-contrast=\"auto\"> for nonprescription drug products.\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">This prior regulatory paradigm limited access to products as either prescription or<\/span> <span data-contrast=\"auto\">nonprescription. This has been particularly impactful for certain classes of drugs for which availability via prescription <\/span><i><span data-contrast=\"auto\">and <\/span><\/i><span data-contrast=\"auto\">nonprescription could be considered safe and valuable.\u00a0\u00a0\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><b><span data-contrast=\"auto\">Provisions of the ACNU Final Rule\u00a0<\/span><\/b><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">On December 23, 2024, the FDA issued a\u202f<\/span><a href=\"https:\/\/www.federalregister.gov\/documents\/2024\/12\/26\/2024-30261\/nonprescription-drug-product-with-an-additional-condition-for-nonprescription-use?mkt_tok=MTU4LUxVTy03OTMAAAGX4ddHpUyLnnFkHuzQpqyCtBNm6nAU4xCnzATC-sLv1yVFv2rLP-pozrtCaC5DWTvX8b5OuivyEF1f-IbIeQ\"><span data-contrast=\"none\">final rule<\/span><\/a><span data-contrast=\"auto\">\u202fto broaden the types of prescription drug products that consumers can purchase OTC, and allow a drug to be marketed with both prescription and non-prescription status. The rule went into effect May 27, 2025, after its original implementation date of January 27, 2025, was postponed twice.<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">The final rule offers manufacturers an approval pathway for a non-prescription drug with ACNU by allowing flexibility when labeling alone cannot convey the necessary information for consumer self-selection or appropriate actual use. Manufacturers would need to submit a new drug application (NDA) or an abbreviated new drug application (ANDA) detailing how the ACNU is operationalized and includes consumer studies. The ACNU would need to demonstrate a \u201cmeaningful difference\u201d between the prescription drug product and its non-prescription counterpart.\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">If the ACNU is accepted as a reasonable mechanism for consumer self-selection, it would be sufficient to account for a \u201cmeaningful difference\u201d between the prescription drug and its non-prescription counterpart <\/span><i><span data-contrast=\"auto\">without <\/span><\/i><span data-contrast=\"auto\">any differences in the drug attributes (e.g., strength).<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><b><span data-contrast=\"auto\">Strategic Considerations for Manufacturers<\/span><\/b><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">Manufacturers will need to carefully plan early if they intend to market their products with both prescription and non-prescription status.<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">If a consumer is unable to appropriately self-identify for use of the product based solely on the label, manufacturers can propose a variety of different ACNU methods to bridge any gap between insufficient labeling and appropriate self-selection. For example, manufacturers can propose that before purchasing the nonprescription drug product, consumers would need to take a questionnaire on a display screen at a pharmacy kiosk or via an automated telephone response system. Consumers will know there is an extra step required before purchasing the drug product from the label. Manufacturers will need to consider what data is needed to show the safety of the drug product when offered OTC with an ACNU, and what ACNU methodology will be accepted by the FDA to ensure consumer adherence, proper self-selection, and clear labeling.<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">There are multiple downstream market access implications, including market share and volume changes, pricing approaches, payer coverage determination, and consumer decision making.\u00a0 Even if a manufacturer is not planning to submit an ACNU non-prescription application for their drug product, manufacturers will want to carefully observe potential market dynamic shifts for an entire class of drugs if one of the products does receive ACNU non-prescription marketing status. Drug classes that may be affected include antihistamines, analgesics, topical pain or itchiness relief creams, acid reducers, oral contraceptives, and potentially other drugs for common chronic diseases.\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><b><span data-contrast=\"auto\">Potential for Added Demand to Pharmacists<\/span><\/b><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">Approval of an ACNU product also has implications for pharmacies, especially if the ACNU product or state law requires intervention by the dispensing pharmacy, such as storing the product behind the counter to facilitate counseling by a pharmacist or requiring a survey to be administered by a pharmacist. Pharmacies will want to consider if there will be an added burden for pharmacists to administer these drugs, if infrastructure changes will need to be made, and if every pharmacy will be providing access to these products.<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><b><span data-contrast=\"auto\">How Relevant Parties Can Prepare for Coming Changes<\/span><\/b><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">The ACNU pathway has the potential to optimize patient access to drugs via two distinct routes associated with unique costs and health plan coverage. Manufacturers, payers, and pharmacies will need to thoroughly consider the various impacts on their organizations when determining the value of the ACNU pathway.\u00a0<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">Avalere Health\u2019s regulatory, payer, and market access experts can help interested parties make informed decisions regarding utilization of this new pathway, as well as with execution of strategies. To discuss how Avalere Health can help industry stakeholders navigate this new approval pathway, <\/span><a href=\"https:\/\/pages.avalere.com\/Keep-In-Touch.html?_gl=1*3hmxv3*_gcl_au*MTk0MTgyMTE3OS4xNzQ1ODY2NDUwLjc2NDkxNDcwNC4xNzQ4NDY3NTkwLjE3NDg0Njc2MDg.*_ga*NzQ4NjQ1Mjc2LjE3NDUzMzE4NzQ.*_ga_1LKSE3H6ZT*czE3NDg0NzA0MzgkbzEyJGcxJHQxNzQ4NDcwNDYyJGozNiRsMCRoMA..\"><span data-contrast=\"none\">connect with us<\/span><\/a><span data-contrast=\"auto\">.<\/span><span data-ccp-props=\"{&quot;335551550&quot;:6,&quot;335551620&quot;:6}\">\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Previous FDA Policy Delineating Prescription and OTC Status\u00a0 Prior to the Additional Condition for Non-prescription Use (ACNU) final rule, FDA regulations only allowed prescription (Rx) drug products to be either fully (\u201cfull Rx-to-over-the-counter [OTC] switch\u201d) or partially (\u201cpartial Rx-to-OTC switch\u201d; e.g., only specific strengths or indications) changed to non-prescription marketing status. This meant that a&hellip;<\/p>\n","protected":false},"author":28,"featured_media":33279,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[3],"tags":[],"content-categories":[891],"class_list":["post-34567","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-insights","content-categories-fda-regulatory-pathways","entry","has-media"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>ACNU Provides a New FDA Approval Pathway for Prescription-to-OTC Drugs | Avalere Health Advisory<\/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:\/\/advisory.avalerehealth.com\/insights\/acnu-provides-a-new-fda-approval-pathway-for-prescription-to-otc-drugs\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ACNU Provides a New FDA Approval Pathway for Prescription-to-OTC Drugs | Avalere Health Advisory\" \/>\n<meta property=\"og:description\" content=\"Previous FDA Policy Delineating Prescription and OTC Status\u00a0 Prior to the Additional Condition for Non-prescription Use (ACNU) final rule, FDA regulations only allowed prescription (Rx) drug products to be either fully (\u201cfull Rx-to-over-the-counter [OTC] switch\u201d) or partially (\u201cpartial Rx-to-OTC switch\u201d; e.g., only specific strengths or indications) changed to non-prescription marketing status. This meant that a&hellip;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/advisory.avalerehealth.com\/insights\/acnu-provides-a-new-fda-approval-pathway-for-prescription-to-otc-drugs\" \/>\n<meta property=\"og:site_name\" content=\"Avalere Health Advisory\" \/>\n<meta property=\"article:published_time\" content=\"2025-06-06T16:00:02+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-06-20T21:53:08+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/advisory.avalerehealth.com\/wp-content\/uploads\/2024\/10\/33205-1-RosalieHoyle-400x600-1.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"600\" \/>\n\t<meta property=\"og:image:height\" content=\"400\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Leah Keller\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@avalerehealth\" \/>\n<meta name=\"twitter:site\" content=\"@avalerehealth\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Leah Keller\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"4 minutes\" \/>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"ACNU Provides a New FDA Approval Pathway for Prescription-to-OTC Drugs | Avalere Health Advisory","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/advisory.avalerehealth.com\/insights\/acnu-provides-a-new-fda-approval-pathway-for-prescription-to-otc-drugs","og_locale":"en_US","og_type":"article","og_title":"ACNU Provides a New FDA Approval Pathway for Prescription-to-OTC Drugs | Avalere Health Advisory","og_description":"Previous FDA Policy Delineating Prescription and OTC Status\u00a0 Prior to the Additional Condition for Non-prescription Use (ACNU) final rule, FDA regulations only allowed prescription (Rx) drug products to be either fully (\u201cfull Rx-to-over-the-counter [OTC] switch\u201d) or partially (\u201cpartial Rx-to-OTC switch\u201d; e.g., only specific strengths or indications) changed to non-prescription marketing status. 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Prior to joining Avalere, Leah conducted policy research and analysis on federal healthcare issues such as Medicaid coverage and payment, commercial insurance coverage and access, healthcare reform, and ACA implementation at the Guttmacher Institute, a thinktank focused on advancing reproductive health and rights. Prior, Leah coordinated data collection, analysis, and publications for George Washington University\u2019s Center for Social Well-Being and Development. Leah holds an MPH in maternal and child health from George Washington University and a BA in anthropology from St. Mary\u2019s College of Maryland.","url":"https:\/\/advisory.avalerehealth.com\/author\/lkelleravalere-com"}]}},"_links":{"self":[{"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/posts\/34567","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/users\/28"}],"replies":[{"embeddable":true,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/comments?post=34567"}],"version-history":[{"count":3,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/posts\/34567\/revisions"}],"predecessor-version":[{"id":34635,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/posts\/34567\/revisions\/34635"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/media\/33279"}],"wp:attachment":[{"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/media?parent=34567"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/categories?post=34567"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/tags?post=34567"},{"taxonomy":"content-categories","embeddable":true,"href":"https:\/\/advisory.avalerehealth.com\/wp-json\/wp\/v2\/content-categories?post=34567"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}