If you have RNA contaminants even with the kit, it is essential to perform RNAse A decontamination, especially if the purity of your DNA sample is of prime importance for post-extraction manipulation.
You can encrease the amount of RNAseA before elution or you can cut out one or multiple agarose gel DNA bands from the same sample and recover the DNA by pooling the gel bands with a DNA gel recovery kit and repeat the preparation step with DNAseA if required.