Clinical Research Directory

Inclusion criteria: * Provide voluntary, written, informed consent to participate in the study * Agree to provide a valid cell phone number and are willing to receive communications through text * Can read and write English * Willing to not begin taking any new supplements during the study and continue taking any supplements they are currently using regularly * Willing to complete questionnaires, records, and diaries associated with the study. * Healthy male and female participants aged 45-75 years * Willing to go to a local blood draw location for a Whole Blood Total Glutathione measurement (baseline and Day 20) * Willing to avoid starting new or stopping any existing dietary supplements throughout the study Exclusion criteria: * Women who are pregnant, breastfeeding, or planning to become pregnant during the trial * Known food intolerances/allergy to any ingredients in the product * Having any of the following conditions: Psychiatric conditions, neurologic disorders, endocrine disorders, cancer * Having had a significant cardiovascular event in the past 6 months * Taking MAO inhibitors, SSRIs, or any other psychiatric or neurological medicines * On immunosuppressive therapy * Adults lacking capacity to consent * Active Smokers * Diagnosed Diabetics