A Clinical Trial to Evaluate the Effects of Super Liver Liquid Drops on Gut Health, Digestive Comfort, and Daily Energy Levels

This is a decentralized (fully virtual), single-group, open-label, prospective clinical trial evaluating the effects of Super Liver Liquid Drops, a liquid botanical dietary supplement, on gut health, digestive comfort, energy levels, and overall well-being over 12 weeks. All 35 enrolled participants will self-administer 2 mL of Super Liver Liquid Drops daily (2 droppers filled to 1 mL each) in the morning with breakfast for the full 12-week intervention period. Participants will complete validated questionnaires and self-reported assessments at Baseline, Week 2, Week 4, Week 8, and Week 12 via the Citruslabs study platform. All study activities will be conducted remotely.

Inclusion Criteria: * Be male or female. * Be aged 30-65 years (inclusive) at the time of enrollment. * Over the past four weeks, has had concerns regarding low energy levels and at least two of the following: Bloating, Digestion, Irregular Bowel movements, Brain fog. * Anyone who is generally healthy - does not live with any uncontrolled chronic disease. * Willing and able to follow the study protocol as described. * Willing to maintain their current diet, exercise routine, and sleep patterns, for the duration of the trial. * If taking other over-the-counter supplements or herbal remedies is willing to maintain this routine without introducing any other new products for the study duration. * Resides in the United States. * Willing to follow the study protocol as described. Exclusion Criteria: * Known allergy or sensitivity to any of the study product ingredients (milk thistle, dandelion, yellow dock, turmeric, ginger, chicory/inulin, berberine). * Known history of severe digestive disorders like acid reflux, Irritable Bowel Syndrome (IBS), Irritable Bowel Disease (IBD), Crohn's disease, or gastrointestinal tract surgeries. * Known history of gallbladder disease or bile duct obstruction. * Has a chronic health condition that could impact participation in this study, such as oncological or psychiatric disorders. * Has a planned surgery in the next 12 weeks. * Currently pregnant, breastfeeding, or planning to become pregnant during the study period. * Known history of substance abuse. * Currently, or was in the past 3 months, a smoker. * Currently participating in or planning to participate in another research study during the study period.