This document discusses the adulteration of crude drugs. It defines adulteration as the incorporation of impurities into genuine drugs, decreasing their quality. There are two types of adulteration: direct/intentional, where an inferior substitute is used; and indirect/unintentional, which occurs without bad intentions through faulty collection, preparation, or storage. Common adulterants include exhausted materials, inferior quality substitutes, foreign matter, and artificially manufactured replacements. Adulteration lowers the amount of active ingredients and can involve inferiority, spoilage, deterioration, admixture, or sophistication.