Inorganic lead-free double perovskites have the advantages of low toxicity, broadband emission, and good stability, which make them promising luminescent materials for lighting applications. However, due to the limited regulation of their self-trapped exciton emission, it is still greatly challenging to achieve white light emitting from a single double perovskite host. Herein, efficient and tunable white light is realized in Cs2NaInCl6: Sb3+, Tb3+, Sm3+ double perovskite by controlling the ratios of the doped three ions with blue, green, and red emissions, respectively. The steady-state and transient fluorescence spectra of singly- and doubly-doped double perovskites reveal the existence of multiple energy transfer channels in the triply-doped phosphors, including from Sb3+ to Tb3+, Sb3+ to Sm3+, and Tb3+ to Sm3+. Benefiting from these channels, the color coordinates of the triply-doped phosphors can cross the whole white light area of the CIE chromaticity diagram by adjusting the ratios of the three dopants, and the maximum internal quantum yield of the white light phosphors is 66.61 %. The white emission phosphors show the characteristic of being independent of excitation wavelength within 310–360 nm. Furthermore, the emission intensity at 430 K of the white light phosphor Cs2NaInCl6: 0.01Sb3+, 0.65Tb3+, 0.20Sm3+ remains 50 % of that at room temperature. A WLED device fabricated with the phosphor and a 365 nm LED chip exhibits a high color rendering index of 90.9, correlated color temperature of 5469 K, and CIE coordinates of (0.333 and 0.328). The results indicate that the as-prepared double perovskite materials are promising candidates in the solid-state lighting field.