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07 Label and refrigerate Mark the vial with the concentration and reconstitution date
IV administration also introduces risks that oral supplementation does not: Contamination or excessive endotoxin exposure Sterility and compounding failures Infusion reactions Venous irritation or infection Dosing errors Additional cost and clinical complexity The FDA has reported adverse events among patients who received injectable compounded glutathione made with an unsuitable dietary ingredient
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This illustration depicts a liposome encapsulating glutathione and its mechanism of penetrating the epidermis and dermis to deliver antioxidants
Beyond 500mcg, the risk-benefit ratio becomes less favorable
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