Recently, solid-state lighting (SSL) technology has been a major breakthrough in lighting systems, contributing notably to both economic and environmental sustainability. Halide double perovskite (HDP) based single component white light emitting semiconductors are currently a hot topic among researchers in the field of SSL technology, as they provide greater structural stability, flexibility, nontoxicity, etc. Herein, we chose Cs 2 AgInCl 6 (CAIC) from the HDP family as our white light emitter owing to its direct bandgap nature and ability to produce broad emission arising from the self-trapped excitons (STE) which are produced by the strong-electron phonon coupling. However, it suffers from low photoluminescence intensity due to its parity-forbidden transition arising from the same even-parity of valence band maximum (VBM) and conduction band minimum (CBM). Thus, Na alloying in Cs 2 AgInCl 6 has been implemented to break the parity via isolation of the [AgCl 6 ] 5− octahedron that restricts the contributions of the Ag-4d orbital in the VBM that induces the odd−even parity transition. To further enhance the luminescence properties of the material, the optimum composition Cs 2 Ag 0.4 Na 0.6 InCl 6 (A4N6) was chosen for transition ion doping (Mn 2+ and Cr 3+ ) to increase photoluminescence properties. Eventually, Cs 2 Ag 0.4 Na 0.6 InCl 6 :Mn6% (A4N6-Mn6) showed a photoluminescence intensity 30 times more than pristine CAIC with a photoluminescence quantum yield (PQLY) of 37.7%, CIE color coordinates (0.36, 0.44), and correlated color temperature of 4757 K. With best-performing materials, we have successfully fabricated a flexible phosphor-based white light-emitting device. It seems that this structural engineering led to the tuning of light from a cold white light region toward a warm white light region that can be efficiently used in household applications. Furthermore, Cs 2 Ag 0.4 Na 0.6 InCl 6 :Mn6% also exhibits the capability of visualizing latent fingerprint (LFP) detection, which will be used for forensic analysis in the future.