A Study to Assess the Gut Health Effects of Oil Compound on Healthy Adults

Exclusion Criteria

• •Pure vegetarians who do not consume chicken, fish and/or egg.
• •Smokers
• •Presence of unstable, acutely symptomatic, or life-limiting illness.
• •Subjects with uncontrolled hypertension with systolic blood pressure ≥160 and diastolic blood pressure ≥100 mm Hg.
• •Subjects with uncontrolled Type II Diabetes Mellitus with FBG ≥ 126 mg/ dl
• •Neurological conditions causing functional or cognitive impairments.
• •Unwillingness or inability to be randomized to one of two intervention groups.
• •Bilateral hip replacements.
• •History or presence of clinically significant renal, hepatic, endocrine, biliary, gastrointestinal, pancreatic or neurologic disorders that, in the judgment of the Investigator, would interfere with the participant's ability to provide informed consent, comply with the study protocol (which might confound the interpretation of the study results), or put the participant at undue risk.
• •History or presence of Irritable Bowel Syndrome as per Rome IV criteria. \[Diagnostic criteria\* Recurrent abdominal pain on average at least 1 day/week in the last 3 months, associated with two or more of the following criteria:
• •1. Related to defecation.
• •2. Associated with a change in frequency of stool.
• •3. Associated with a change in form (appearance) of stool. \*Criteria fulfilled for the last 3 months with symptom onset at least 6 months prior to diagnosis\]
• •Use of any psychotropic medication within four weeks of screening and throughout the study.
• •Use of antibiotics or signs of active systemic infection at the time of screening. Treatment visits will be rescheduled to the subject to wash off the antibiotic for at least five days prior to any test visit.
• •Subject states they regularly consume supplemental enzymes and are unwilling to stop at least one week prior to screening and throughout the study. Supplemental enzymes may include standalone enzyme supplements, probiotic supplements with enzymes, and any medications containing enzymes.
• •Subject states they regularly consume probiotic, prebiotic, energy and mood enhancing supplements supplements and are unwilling to stop at least one week prior to screening and throughout the study. Supplemental probiotics may include standalone probiotic supplements, vitamins with probiotics, and any foods supplemented with probiotics
• •Subject states they are currently being prescribed (by primary care physician or other health professional) medication or using an over-the-counter product that in the opinion of the study physician will have an effect on food digestion or nutrient absorption during the study.
• •Exposure to any non-registered drug product within 3 months prior to the screening visit.
• •Unable/unwillingness to complete study specific diaries (digital/paper-based).
• •Current use of the following medications: monoamine oxidase inhibitors, prescription or herbal weight loss medications/ dietary supplement.
• •Females who are pregnant/planning to be pregnant/lactating or taking any oral contraceptives.
• •Heavy alcohol drinkers defined as follows:
• •For men, consuming more than 4 drinks on any day or more than 14 drinks/week For women, consuming more than 3 drinks on any day or more than 7 drinks/week