A Randomised Clinical Study to Evaluate the Effectiveness and Safety of a Polyherbal Formulation in Preventing Morning Hangover

INTERVENTION: Intervention1: Nil: Nil CONDITION: PRIMARY OUTCOME: 1.Difference in hangover severity scores. 2. Difference in blood and urine markers.Timepoint: Day 0 and 1 SECONDARY OUTCOME: nilTimepoint: nil INCLUSION CRITERIA: Participant must meet all the below criteria in order to be eligible to participate in the study 1 Occasional social alcohol drinkers, aged between 25 to 45 years of either gender 2 Normal BMI range from 18.5 to 24.9 kgperm2 3 Participants willing and able to comply with the alcohol consumption, blood withdrawal requirements and overnight stay as per the study requirements. 4 Participants judged by the Investigator to be in general good health based on medical history and laboratory investigations. 5 Participants understand the study procedures and sign informed consent forms to participate in the study. 6 Women of childbearing potential and men with partners of childbearing potential must agree to use adequate contraception prior to study entry, for the duration of study participation.