To evaluate effects of an ayurvedic formulation in management of increased lipid and cholesterol levels

INTERVENTION: CONDITION: Health Condition 1: E785‐ Hyperlipidemia, unspecified PRIMARY OUTCOME: Reduction of LDL‐C and LipidsTimepoint: up to 12 weeks SECONDARY OUTCOME: Change in clinical symptomsTimepoint: up to 12 weeks INCLUSION CRITERIA: 1) Male or female aged more than and equal to 30 years and less than and equal to 70 years 2) Body mass inde Xbetween 18 Kgperm2 and 35 Kgperm2 3)Total cholesterol level between 200 and 280 mgperdL andor LDL‐C between 130 mgperdL and 190 mgperdL TGless5percentage) 3)The intervention strategy does not require a pharmacological lipid‐lowering intervention, according to any ICMR guidelines 4)Subjects who can communicate, make themselves understood and comply with the requirements of the study 5)Subjects who agree to participate in the study and have dated and signed the informed consent form