The goal of this clinical trial is to evaluate a nutritional supplement in an otherwise healthy adult population. The main questions it aims to answer are: * Do antioxidant carotenoid levels increase in after supplementation as measured by a non-invasive device? * Do wellness factors correlate with supplementation? Researchers will compare the nutritional supplement arm to a placebo group to assess its effects. Participants will take either the nutritional supplement or placebo once daily for 8 weeks. Participants will be scanned by a non-invasive hyperspectral absorption device to obtain a skin carotenoid score. Participants will also have facial images taken, dermal spectrophotometry measurements of their face, and complete self-assessment questionnaires.
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Skin carotenoid score via Prysm iO device
Timeframe: 8 weeks
Short-Form 36 Health Survey
Timeframe: 8 weeks
Skin color measurement via Spectrophotometer
Timeframe: 8 weeks
Perceived Immunity
Timeframe: 8 weeks
Psychological Scales Related to Physical Condition
Timeframe: 8 weeks
Fatigue and Vitality Status Assessment
Timeframe: 8 weeks
Brief Resilience Scale (BRS)
Timeframe: 8 weeks