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Indeed, CDER Acting Director Michael Davis reinforced the policy point publicly on X, emphasizing that compounded GLP1 products are not FDAapproved and have not undergone the rigorous review for safety, efficacy, and manufacturing quality that is required for drugs approved through the new drug application (NDA) or abbreviated new drug application (ANDA) pathways.[3] This is now the third major set of warning letters in less than a year with the majority aimed at telehealth marketing of compounded GLP-1 products: September 2025: roughly 80 warning letters and 40 untitled letters March 2026: 30 warning letters June 2026: 25 warning letters The Claims FDA Is Targeting As in earlier rounds, the June 2026 letters appear highly standardized and focus on consumerfacing promotion of compounded GLP-1 products
Joint and Soft-Tissue Research Applications The 99 Purity Peptides product page positions KLOW specifically for "joint and soft-tissue recovery blend" research models of chronic joint stress, tendon and ligament overload, and long-term soft-tissue wear
Address the Underlying Issue If the reason is addressable, work with your provider
(Going caffeine free with Thesis removes both the caffeine and L-theanine content from the blends, unfortunately.) Generally, participants in studies are given about 2.5mg/kg of L-theanine, meaning a person who weighs 150lb would take 170mg of L-theanine
& Bisanti, L
: BPC-157 ()
