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Because of its potency, IV glutathione must always be administered under medical supervision, following proper assessment, dosing protocols, and safety standards

Aspergillus saitoi and Penicillium roquefortii IFO 5956 contain a bioactive compound (2,3-dihydroxybenzoic acid) with high antioxidant properties

AOD-9604 FDA Approval History At a glance FDA approval status / Never approved for any indication in the United States NDA filing history / No New Drug Application has ever been submitted to FDA Chemical identity / Synthetic peptide corresponding to amino acids 176-191 of human growth hormone, with a tyrosine residue added at the C-terminus Developer / Metabolic Pharmaceuticals Ltd (Melbourne, Australia), now defunct Clinical trial outcome / Phase IIb trial (2007) failed to meet primary efficacy endpoint for obesity FDA compounding status / Placed on Category 2 list

Aiding the bodys detoxification process, it strengthens the immune system and adrenalin synthesis, offering liver support during illness and times of stress