Hydrogen peroxide was determined in oral antiseptic and bleach samples using a flow-injection system with amperometric detection. A glassy carbon electrode modified by electrochemical deposition of ruthenium oxide hexacyanoferrate was used as working electrode and a homemade Ag/AgCl (saturated KCl) electrode and a platinum wire were used as reference and counter electrodes, respectively. The electrocatalytic reduction process allowed the determination of hydrogen peroxide at 0.0 V. A linear relationship between the cathodic peak current and concentration of hydrogen peroxide was obtained in the range 10–5000 μmol L−1 with detection and quantification limits of 1.7 (S/N = 3) and 5.9 (S/N = 10) μmol L−1, respectively. The repeatability of the method was evaluated using a 500 μmol L−1 hydrogen peroxide solution, the value obtained being 1.6% (n = 14). A sampling rate of 112 samples h−1 was achieved at optimised conditions. The method was employed for the quantification of hydrogen peroxide in two commercial samples and the results were in agreement with those obtained by using a recommended procedure.