The Effects of a Novel Nutritional Product on Nutrient Gaps and Gut Health in Active Adults

Inclusion Criteria: * Provide voluntary signed and dated informed consent. * Be in good health as determined by medical history and routine blood chemistries. * \> 1 year of resistance training experience (minimum of 2 days per week of resistance training session with free weights) * Age between 18 and 40 yr (inclusive). * Subject agrees to maintain existing dietary and physical activity patterns throughout the study period. * Subject is willing and able to comply with the study protocol. Exclusion Criteria: * History of unstable or new-onset cardiovascular/cardiorespiratory, liver, or renal conditions. * History of diabetes or endocrine disorder. * History of use of medications or dietary supplements known to confound the study or its endpoints. * Alcohol consumption (more than 2 standard alcoholic drinks per day or more than 10 drinks per week) or drug abuse or dependence within the past 6 months. * Current smokers or smoking within the past month. * History of hyperparathyroidism or an untreated thyroid condition. * History of malignancy in the previous 5 years except for non-melanoma skin cancer (basal cell cancer or squamous cell cancer of the skin). * Prior gastrointestinal bypass surgery (Lapband), etc. * Other known gastrointestinal or metabolic conditions that might impact nutrient absorption or metabolism, e.g., short bowel syndrome, Irritable bowel syndrome (IBS), diarrheal illnesses, history of colon resection, gastro paresis, Inborn-Errors-of-Metabolism (such as PKU). * Chronic inflammatory condition (e.g., rheumatoid arthritis, Crohn's, ulcerative colitis, Lupus, HIV/AIDS, etc.). * Previous medical diagnosis of asthma, gout, or fibromyalgia. * Pregnant women, women trying to become pregnant, women less than 120 days postpartum or nursing women. * Known sensitivity to any ingredient in the test formulations as listed in the product label. * Currently participating in another research study with an investigational product or have been in another research study in the past 30 days. * Any other conditions that, in the opinion of the medical staff, could confound the primary endpoints or place the subject at increased risk of harm if they were to participate.