A Study to Evaluate Safety and Health Benefits of Basis™ Among Elderly Subjects.

Inclusion Criteria: * Males or females 60 to 80 (inclusive) years of age * Body Mass Index (BMI) must be 18 to 35 kg/ m2 (±1 kg/m2) * •Be able to make scheduled office visits 4 times during the study * Willing to follow the instructions and complete multiple study questionnaires and assessments * Agrees to avoid taking Vitamin B3 (Niacin, Nicotinic acid or niacinamide) supplements or multivitamins 14 days prior to randomization and for the duration of the study period * Healthy otherwise as determined by laboratory results and medical history * Has given voluntary, written, informed consent to participate in the study Exclusion Criteria: * History of any significant chronic disease or any clinically active illness within 3 months of study entry, including any history of renal or liver impairment, any endocrine, inflammatory, cardiovascular, gastro-intestinal, neurological, psychiatric, neoplastic or metabolic disease. Clinical significance of disease will be assessed by the Qualified Investigator and eligibility determined. * Significant or untreated medical disorders including recent myocardial ischemia or infarction, unstable angina, uncontrolled hypertension, AIDS, malignancy, epilepsy, and recent cerebrovascular disease * Subjects with or who have recently experienced a traumatic injury, infections or undergone surgery * Subjects with history of pellagra or niacin deficiency * Taking lipid lowering drugs * Use of natural health products containing Nicotinamide riboside within 14 days prior to randomization and during the course of the study * History of or current diagnosis of any cancer (except for successfully treated basal cell carcinoma) diagnosed less than 5 years prior to screening. Volunteers with cancer in full remission more than 5 years after diagnosis are acceptable * Has participated in any clinical trial with an investigational medicinal product within the past three months prior to the first dose in the current study * Unstable medical conditions * Alcohol use \>2 standard alcoholic drinks per day * History of alcoholism or drug abuse within 1 year prior to screening * History of significant allergies * Allergy or sensitivity to any of the investigational product ingredients * Use of medicinal marijuana * Clinically significant abnormal laboratory results at screening * Individuals who are cognitively impaired and/or who are unable to give informed consent * Any other condition which in the Investigator's opinion may adversely affect the participant's ability to complete the study or its measures or which may pose significant risk to the participant