Phyllantus Amarus for the Protection of Liver Health

Inclusion Criteria:

- Healthy male or female 21-50 years of age, inclusive.

- Subject consumes at least 5 servings of alcohol per week on a regular basis.

- Minimum POMS score of 15.

- Access to a computer and internet

- Subject is willing to maintain his or her habitual food and beverage intake (other
than substitution of study food for similar products) and physical activity patterns
throughout the study period.

- Body mass index (BMI) between 20 and 30 kg/m2.

- Subject is willing and able to comply with the alcohol consumption requirements.

- Subjects willing to stay in the clinic for two overnight stays

- Judged by the Investigator to be in general good health on the basis of medical
history.

- Subject understands the study procedures and signs forms providing informed consent to
participate in the study and authorization for release of relevant protected health
information to the study investigator.

Exclusion Criteria:

- Any Liver condition including Hepatitis, Fatty Liver, Liver Disease.

- Liver Function greater than three times the upper level limit of normal

- History or record of aggressive or violent behavior

- Any significant GI condition that would potentially interfere with the evaluation of
the study product [e.g., Ulcerative Colitis or Crohn's Disease, inflammatory bowel
disease, irritable bowel syndrome, Clinically significant Gastritis, history of upper
GI bleed (bleeding ulcer), chronic constipation (defined as <3 bowel movements per
week), history of frequent diarrhea, history of surgery for weight loss,
gastroparesis, clinically important lactose intolerance].

- Clinically significant renal, hepatic, endocrine (including diabetes mellitus),
cardiac, pulmonary, pancreatic, neurologic, or biliary disorder.

- Known allergy or sensitivity to any ingredients in the study products.

- Extreme dietary habits (e.g., vegan, Atkins Diet, etc.).

- Recent (within two weeks of visit 1, week -1) episode of acute gastrointestinal
illness such as nausea, vomiting, or diarrhea.

- Uncontrolled hypertension (systolic blood pressure _160 mm Hg or diastolic blood
pressure _100 mm Hg at visit 1, week -1).

- History or presence of cancer in the prior two years, except for non-melanoma skin
cancer.

- Any major trauma or surgical event within three months of visit 1, week -1.

- Recent use of antibiotics (within 6 weeks).

- Females who are pregnant, lactating, planning to be pregnant during the study period.

- Recent history of (within 12 months) or strong potential for alcohol or substance
abuse. Alcohol abuse will be defined as >14 drinks per week (1 drink =12 ounces beer,
5 ounces wine, or 1 ½ ounces distilled spirits).

- Participation in a clinical study with exposure to any non-registered drug product
within 30 days prior.

- Individual has a condition the Investigator believes would interfere with his or her
ability to provide informed consent, comply with the study protocol, which might
confound the interpretation of the study results or put the person at undue risk

- Current active respiratory illness at the time of screening

- Any immune system disorders

- Subjects with a history of perforation of the stomach or intestines

- Subjects who have had gastric bypass surgery

- Untreated Hypothyroidism

- Subjects with active eating disorder including anorexia nervosa, bulimia, and/or
obsessive compulsive eating disorders

- Spinal cord injuries