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) .