Objective:To establish a method of flavone and organic acid compounds by HPLC fingerprint, providing the basis for whole control and evaluating the quality of medicinal materials. Method: The separation was performed on an BDS C18(4.6 mm×250 mm, 5 μm) column of Hypersil. The mobile phase was methanol-0.1% phosphoric acid solution, gradient elution. The flow rate was 1.0 mL·min-1 and the wavelength was set at 330 nm. Result: HPLC fingerprint of flavone and organic acid compounds was established. found 17 co-possessing peaks, RSD of precision and reproducibility was in the range of<5%, and the similarity of 13 batches of Glechoma longituba (Nakai) Kupr was between 0.713-0.987. Conclusion: This method is simple and accurate, reproducible and can be used to provide a base for the quality of the herbs.