A Parallel Study Evaluating the Safety of Lactospore® in Healthy Individuals

Inclusion Criteria: * Male or female ≥18 years of age * If female, subject is not of child bearing potential or female subject of childbearing potential must agree to use a medically approved method of birth control and have a negative urine pregnancy test result. * Healthy as determined by laboratory results and medical history * Normal BMI 18.5 - 29.9 kg/m2 * Has given voluntary, written, informed consent to participate in the study Exclusion Criteria: * Women who are pregnant, breastfeeding, or planning to become pregnant during the course of the trial * Subject has any clinically significant medical conditions * Subject requires the use of prescribed medications (other than birth control) * Use of illicit drugs or history of drug or alcohol abuse with the past 5 years (currently having more than 2 standard alcoholic drinks per day) * Participation in a clinical research trial within 30 days prior to randomization * Clinically significant abnormal laboratory results at screening * Allergy or sensitivity to test product ingredients * 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 subject's ability to complete the study or its measures or which may pose significant risk to the subject