There are so many herbal products in market e.g., Cough syrup, Constipation herbal medicines or others, which claim to contain several herbal extract (Botanical ingredients). Each Botanical extract is comprised of thousands of macro and micro molecules of different classes/groups of molecules in different concentrations?

Regulatory agencies expects quality control and claims of these ingredients parallel to synthetic drugs, which are based on absolute molecule (Enriched to 99% plus) and not possible in Herbal medicines.

Moreover, degradation during Shelf life studies made mandatory have also been asked for? How come it is possible and how one can support Herbal medicines or Regulatory agencies not to consider herbal medicines parallel to synthetic drugs as Herbal medicines are based on Holistic Science.

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