A Clinical Study to Assess the Effect of a Supplement on Digestive Health, Overall Well-being, and Participant Experience.

Inclusion Criteria: * Male or female. * Aged 18-65 years. * Willing to comply with study requirements. * No known allergies to the ingredients listed in the product. * Self-reported mild digestive issues (e.g., occasional bloating, stomach discomfort, occasional constipation, or occasional diarrhea). * Generally healthy - do not live with any uncontrolled chronic disease . Exclusion Criteria: * Pre-existing chronic conditions that would prevent adherence to the protocol, including oncological and psychiatric disorders. * Known severe allergic reactions that require an Epi-Pen. * Women who are pregnant, breastfeeding, or attempting to conceive. * History of severe diagnosed digestive disorders (e.g., IBS, IBD, Crohn's disease) or gastrointestinal-tract surgeries. * Unwillingness to follow the study protocol. * Invasive medical procedure within the last three weeks or planning one during the study period. * History of substance abuse. * Current participation or planning to participate in another research study. * Regular consumption of probiotics, fiber, or prebiotic supplements within 3 weeks of the study. * Regular intake of medications that may interfere with the study or study product (e.g., anticoagulants, laxatives, sedatives, beta-blockers, anti-acids) .