Indoor gas-phase radical sources are poorly understood but expected to be much different from outdoors. Several potential radical sources were measured in a windowless, light-emitting diode (LED)-lit room in a college athletic facility over a 2 week period. Alternating measurements between the room air and the supply air of the heating, ventilation, and air-conditioning system allowed an assessment of sources. Use of a chlorine-based cleaner was a source of several photolabile reactive chlorine compounds, including ClNO 2 and Cl 2 . During cleaning events, photolysis rates for these two compounds were up to 0.0023 pptv min −1 , acting as a source of chlorine atoms even in this low-light indoor environment. Unrelated to cleaning events, elevated ClNO 2 was often observed during daytime and lost to ventilation. The nitrate radical (NO 3 ), which is rapidly photolyzed outdoors during daytime, may persist in low-light indoor environments. With negligible photolysis, loss rates of NO 3 indoors were dominated by bimolecular reactions. At times with high NO 2 and O 3 ventilated from outdoors, N 2 O 5 was observed. Elevated ClNO 2 measured concurrently suggests the formation through heterogeneous reactions, acting as an additional source of reactive chlorine within the athletic facility and outdoors.