The Efficacy of Amway Herbal Drink to Improve Skin Anti-aging

Inclusion Criteria:

• Male and female subjects, aged 30 to 60 years, with a gender ratio of 3:7;
• Subjects are healthy;
• Visual assessment, smoothness is greater than or equal to 3 points (according to theTest Method of Efficacy Measurement of Nourishing Cosmetic Products issued by ChineseAssociation of Fragrance Flavor and Cosmetic Industries, the smaller the index, thebetter. Please refer to appendix II);
• Visual assessment, the gloss index is greater than or equal to 4 points (according tothe Unilever Radiance Scale, the smaller the index is the better. Please refer toappendix III);
• Subjects could not use facial whitening and moisturizing products during the trial;
• Agree not to take other oral products with similar efficacy (such as collagen, sodiumhyaluronate, etc.) during the trial. During the trial, participants agreed not to takeany drugs or supplements. Do not do any medical beauty projects during the trial, donot participate in other interventional clinical research;
• Have a full understanding of the purpose, benefits, and possible risks and sideeffects of the study;
• Willing to comply with all research requirements and procedures;
• Understand the test procedure, read, and sign an appropriate Informed Consent Formindicating their willingness to participate.

Exclusion Criteria:

• Use of any medications or supplements that may alter skin properties during the first 3 months of enrollment;
• Skin disease patients;
• Ggastrointestinal symptoms being treated;
• Lactose intolerance, allergy to fish and its products;
• Present with other organic diseases that affect intestinal function, such as historyof gastrointestinal resection, colon or rectal cancer, inflammatory bowel disease,diabetes, hyperthyroidism or hypothyroidism, congenital megacolon, scleroderma,anorexia nervosa, etc.;
• Controlling diet, exercising more, or taking medications to control weight or affectappetite in the last 3 months;
• Subjects have any of the following medical history or clinical findings that mayaffect the evaluation of the trial effect: significant gastrointestinal disorders,liver, kidney, endocrine, hematological, respiratory and cardiovascular diseases;
• Abuse of alcohol or other illicit drugs, supplements currently or in the past, or OTCprescription drugs that may cause intestinal dysfunction or interfere with theevaluation of trial effects;
• Frequent use of drugs that may affect gastrointestinal function or the immune system,as judged by the researcher;
• Use of laxatives or other digestive substances in the 2 weeks prior to trialcommencement;
• Women who are pregnant or breastfeeding, or who plan to become pregnant during thetrial;
• PI considers that volunteers cannot fully cooperate with the trial arrangement.