Total differential scattering angular distribution measurements for He scattering from Cl2 are reported. The scattering data are combined with previous excitation spectroscopy and vibrational predissociation product state distributions for He-Cl2 to determine the potential-energy surfaces for the ground X and excited B electronic states. The potentials are somewhat deeper, D(e) = -38.2 cm-1 for the X state, than previously estimated. The X state potential minimum is for the ''T'' shaped configuration with a R(min) value of 3.55 angstrom. The potentials are quite successful at describing the scattering data, the rotationally resolved spectroscopy of the complex, and the product state distributions for vibrational predissociation. The B state potential underestimates the dependence of the rate of vibrational predissociation on the initial vibrational level.