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Its defining pharmacological characteristic relative to its predecessors (GHRP-2, GHRP-6) is its selectivity: at doses exceeding 200-fold the GH-release ED, ipamorelin does not stimulate significant release of adrenocorticotropic hormone (ACTH), cortisol, prolactin, FSH, LH, or TSH, in animal studies

Our products are cosmetic personal-care items for external use and are not intended to diagnose, treat, cure or prevent any disease

Be "along for the journey" as customers cycle on and off medications, rather than committing everything to one demographic that might shrink next year

Do not apply the powder directly to the skin or scalp