Traditional kinetics of electronically excited products of O3 and O2 photolysis is supplemented with the processes of energy transfer between vibrational-electronic excited states of the O2 and the O2 molecule in the ground state. When vibrational-electronic kinetics of excited products of ozone and oxygen photolysis is taken into account, the ozone concentration profiles retrieved separately from measured intensities of 762 nm and 1.27 mkm emissions turn out to be in a good agreement.