The long moratorium on state control (supervision) over the activities of business entities has led to an increase in the volume of unregistered, low-quality, counterfeit and counterfeit veterinary products on the Ukrainian market. Violations by manufacturers regarding the entry into circulation of dangerous products are also due to the long absence of licensing of production and sale of products for veterinary medicine and animal husbandry. In these circumstances, there are numerous complaints from consumers about the low quality and safety of veterinary drugs, feeds, feed additives and premixes. The article covers the issues of examination of product appearance, labeling, primary (group) and secondary (transport) packaging, which is carried out in order to establish the conformity of manufactured products to the requirements declared in the regulatory documentation, which will identify dangerous products on the domestic market. In carrying out the examination of veterinary goods presented by consumers and other enterprises or institutions, the general procedure for its conduct shall be established. They check the completeness of the sent materials and check their availability with the corresponding list in the cover letter, open the sealed samples by commission and find out whether the veterinary drug has been registered in Ukraine. Then the data presented in the materials are compared with the registration materials and normative documentation, and a protocol of product inspection for compliance with the requirements declared in the dossier, registration certificates, technical conditions, quality certificates, etc. is drawn up. Examination of the appearance of the label is carried out visually, comparing with the original or with the materials of the relevant registration dossier. Check the correct labeling and packaging of products, and it is important to pay attention to the statement of the summary product of characteristics.
 As a result of the procedures for assessing the correctness and reliability of the appearance of veterinary products in accordance with the original sample, registration dossier and regulatory documentation, a conclusion is issued, which provides a detailed description of the research and the conclusions drawn from their results.