A Study to Investigate the Efficacy of Pain Bloc-R in Healthy Participants With Non-pathological Aches and Discomfort

A randomized, double‐blind, placebo‐controlled, cross‐over pilot study to investigate the efficacy of Pain Bloc‐R in healthy participants with non‐pathological aches and discomfort. The study will have 3 study periods. During each study period, eligible participants will consume either Pain Bloc‐R, comparator product, or placebo for 7 days during each study period (1 product per study period), with a 1‐week washout period in between each period. The primary objective is the comparison of change in unresolved aches and discomfort from pre‐supplement to Day 7 between the Pain Bloc‐R, comparator, and placebo, as assessed by the Brief Pain Inventory (BPI) questionnaire.