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Published clinical trials report a favorable safety profile for GHK-Cu with low rates of mild observations including localized application site irritation (5%), transient skin redness (3%), and itching (2%)

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What happened was that NMN was being studied as an Investigational New Drug (IND), and as such, it could no longer be designated as a dietary supplement and would need FDA authorization for administration in humans.26 27 The prohibition was subsequently met with a lawsuit that led to a federal court ruling in 2024 that suspended legal proceedings on the case and allowed NMN to continue being sold as a supplement, at least for now

Preparing the injection site involves the following steps: Select a clean, well-lit area for the injection site