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On February 6, 2026, however, the FDA’s approach appeared to shift with an announcement that it would be taking steps to restrict GLP-1 active pharmaceutical ingredients (APIs) that continue to be used in non–FDA-approved compounded products, as well as to combat “misleading direct-to-consumer advertising and marketing.” Unequivocally, the FDA warned: “Entities engaged in the manufacture, distribution, or marketing of unapproved compounded GLP-1 products should be aware that failure to adequately address any violations may result in legal action without further notice, including, without limitation, seizure and injunction.” The FDA specifically named Hims & Hers, a popular and outspoken telehealth provider that advertises compounded GLP-1 products, in the announcement

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Keep Records: Retain all receipts and any additional documentation required by your FSA plan for reimbursement, including the prescription and a reimbursement form