The present work outlines the implementation and performance of two cost efficient post-SCF extensions into the third-order SCC-DFTB code. The first one, the charge model 3 (CM3), corrects for errors in bond dipoles for an improved description of molecular charge distribution as compared to the standard Mulliken partitioning scheme. The second one focuses on the response of the charge density, that is, the electronic molecular polarizability, described inaccurately from SCC-DFTB due to the usage of a minimal atomic orbital basis. Here, a variational approach, based on scaled dipole integrals, was implemented, which clearly outperforms standard finite electric field approaches for polarizability calculations by approximately 1 order of magnitude. Both extensions in the present work rely on a set of empirical parameters, which were fitted against 112 organic molecules to match a reference data set from full density functional calculations with a large basis. As an achievement, notably improved electronic properties, that is, molecular dipole moments and polarizabilities, result from SCC-DFTB calculations at negligible additional computational cost. Furthermore, the accuracy of infrared and Raman intensities was tested as first-order derivatives of the new dipoles and polarizabilities as a function of normal mode vibrations. As a result, the current implementations cannot contribute to an improved prediction of relative intensity pattern from SCC-DFTB as compared to ab initio reference data.