Objectives To investigate the prohibited matters in antimicrobial products for further supervision.
Methods Sixteen kinds of prohibited matters in 67 antimicrobial product samples selected by random were inspected, analyzed and evaluated according to relevant standards and analytical methods.
Results Prohibited matters were detected in 35 samples, and the unqualified rate was 52.2%.
Conclusions The violation of adding prohibited matters into antimicrobial products was serious, and the supervision should be strengthened in the future.