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At present, regulatory agencies like the FDA and the European Commission evaluate CQDs on a case-by-case basis, irrespective of a specific regulatory procedure as these nanomaterials do not fit neatly within existing classifications for pharmaceuticals, biologics, or medical devices [172]

The patches deliver actives directly to the thin under-eye skin without the device stamping action

A prescription from a primary care physician or licensed medical doctor practicing within the USA is required

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Cost considerations factor into stacking decisions

This takes time