Objective: To establish a method for simultaneous determination of ten active ingredients(jasminoidin,peoniflorin,naringin,hesperidin,jatrorrhizine hydrochloride,baicalin,berberine hydrochloride,emodin,chrysophanol,aloe-emodin). Methods: The determination was carried out with MERCK chromolith RP-18e column(100 mm×4.6 mm).The mobile phase consisted of acetonitrile(A)-0.1% phosphoric acid solution(B) with gradient elution(0-2 min,8%A;2-10 min,8%A→25%A;10-23 min,25%A→70%A) at a flow rate of 2.0 mL·min-1.The detection wavelengths were 230 nm in 0-11.0 min(for determination of jasminoidin,peoniflorin,naringin,hesperidin,jatrorrhizine hydrochloride,baicalin,berberine hydrochloride),and 254 nm in 11.0-23.0 min(for determination of emodin,chrysophanol,aloe-emodin). Results: The calibration curves were linear in the ranges of 9.94-198.8 μg·mL-1 for jasminoidin(r=0.9997),10.19-203.8 μg·mL-1 for peoniflorin(r=0.9996),10.23-204.6 μg·mL-1 for naringin(r=0.9998),10.48-209.6 μg·mL-1 for hesperidin(r=0.9996),10.11-202.2 μg·mL-1 for jatrorrhizine hydrochloride(r=0.9998),10.31-206.2 μg·mL-1 for baicalin(r=0.9997),10.84-216.8 μg·mL-1 for berberine hydrochloride(r=0.9998),10.39-207.8 μg·mL-1 for emodin(r=0.9997),10.22-204.4 μg·mL-1 for chrysophanol(r=0.9998),10.42-208.4 μg·mL-1 for aloe-emodin(r=0.9998).The average recoveries(n=6) were 98.8%,97.2%,97.4%,98.3%,99.2%,98.5%,97.9%,98.1%,98.2% and 97.6%;RSDs were 1.1%,1.2%,1.0%,1.2%,1.0%,1.3%,1.5%,1.2%,1.3% and 1.5%,respectively. Conclusion: The method is simple and repeatable,which can be applied to the quality control of Mingmu Shangqing tablets.