The tapping of municipal wastewater for potable reuse significantly enhances drinking water supply in drought-stricken regions worldwide. Membrane-based potable reuse treatment trains commonly employ ultraviolet-based advanced oxidation processes (UV-AOPs) to degrade trace organic contaminants in water to produce high-quality recycled water. Hydrogen peroxide (H 2 O 2 ) is used as the default photo-oxidant. Meanwhile, chloramines, which are added to prevent biofouling, pass through the membranes and impact the treatment efficiency of UV-AOP. Water reuse facilities therefore face the dilemma of optimizing H 2 O 2 (an added photo-oxidant) and chloramines (a carry-over photooxidant) doses. Utilizing a uniquely designed pilot-scale reactor and real-time recycled water, we evaluated treatment efficiencies of UV-AOP on six important indicator contaminants, with monochloramine (NH 2 Cl) and H 2 O 2 as photo-oxidants. Hydroxyl radical (HO • ) and reactive chlorine species, such as the chlorine atom (Cl • ) and chlorine dimer (Cl 2•− ), were the major reactive species. Overall, radicals generated from photolysis of NH 2 Cl alone achieved removal of indicator compounds, which can be further improved by optimizing UV fluence, i.e., the UV dose. Furthermore, the addition of H 2 O 2 enhanced HO • formation and improved contaminant removal. However, the addition of H 2 O 2 , when the background NH 2 Cl level was above 2 mg L −1 (as Cl 2 ), provided limited improvement in treatment efficiency. These trade-offs between chloramine and H 2 O 2 as oxidants, and the recommended optimization of the associated effective UV fluence, are critical for energy-efficient and costeffective potable reuse to address the challenges of global water scarcity.