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The growing popularity of L-glutathione for skin whitening has sparked a debate within the medical community
FDA guidance for RUO-labeled in vitro diagnostic products explains that RUO labeling is meant to identify materials in a laboratory research phase and distinguish them from diagnostic contexts [16]
The FDA may not approve these as there is insufficient high-quality human clinical evidence demonstrating safety and effectiveness as we would normally see in a Pre Clinical and Clinical Trial Ph 1-4 study
Clinical trials are ongoing, and Novo Nordisk has indicated plans to file for approval
Dimet-Wiley, A
Together they address repair from both the vascular supply side and the cellular mechanics side
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