Probiotic Research On Safety, Palatability, Efficacy and Receptivity

Inclusion Criteria: * Non-pregnant and non-lactating * English speaking with the ability to give informed consent * 18-40 years of age (inclusive) * Women who are biologically female * Willing and able to agree to the requirements and lifestyle restrictions of this study * Able to understand and read the questionnaires in English and carry out all study-related procedures * Located in the greater Ottawa area and a resident of Ontario Exclusion Criteria: * Individuals who are lactating, pregnant, or planning to become pregnant during the study * Individuals who are not maintaining adequate birth control measures * Adequate birth control measures include any option that will adequately prevent pregnancy including: contraceptives, lifestyle choices, complete abstinence, or as a result of other medical methods, procedures, or conditions * Have a known sensitivity, intolerability, or allergy to any of the study products or their excipients * Are using vitamin and mineral supplements containing B vitamins * Intake of a B-vitamin-containing micronutrient supplement or probiotic product in the previous 4 weeks * Expecting to change diet and exercise regimen in the next 4 weeks * Have planned surgery during the course of the study * Use of investigational product(s) in another research study within 30 days prior to the baseline visit or during the study duration * Taking probiotics during the study period * More than 2 alcoholic beverages per day throughout the duration of the study * Known medical history of specific conditions including: Gastrointestinal disorders: celiac disease, ulcerative colitis, and Crohn's disease; Gastric cancer and gastric polyps; Inflammatory bowel diseases; Helicobacter pylori infection; Gastrectomy, duodenal bypass, bariatric surgery