What should be stated on the label of prepackaged food?

The content is as follows:\x0d\Article 67 There should be labels on the packages of prepackaged foods. The label should indicate the following matters: \x0d\ (1) Name, specifications, net content, and production date; \x0d\ (2) Ingredients or ingredients list; \x0d\ (3) Name, address, and contact information of the producer;\x0d\ x0d\(4) Shelf life;\x0d\(5) Product standard code;\x0d\(6) Storage conditions;\x0d\(7) Common names of the food additives used in national standards;\x0d\(8 ) Production license number; \x0d\ (9) Other matters that should be indicated by laws, regulations or food safety standards. \x0d\The labels of main and complementary foods designed for infants and young children and other specific groups of people should also indicate the main nutritional ingredients and their contents. \x0d\If national food safety standards have other provisions on labeling matters, those provisions shall prevail. \x0d\Article 69 The production and operation of genetically modified foods must be clearly marked in accordance with regulations. \x0d\Article 70 Food additives should have labels, instructions and packaging. Labels and instructions shall state the matters stipulated in Items 1 to 6, 8 and 9 of Paragraph 1 of Article 67 of this Law, as well as the scope, dosage and method of use of food additives, and shall be stated on the label. The words "food additives" are clearly marked on the label. \x0d\Article 71 Labels and instructions for food and food additives must not contain false content or involve disease prevention or treatment functions. Manufacturers and operators are responsible for the contents of labels and instructions they provide. \x0d\The labels and instructions of food and food additives should be clear and obvious, and the production date, shelf life and other matters should be clearly marked and easy to identify. \x0d\Foods and food additives that are inconsistent with the contents of their labels and instructions shall not be put on the market for sale. \x0d\Article 72 Food operators shall sell food in accordance with the warning signs, warning instructions or precautions indicated on food labels. \x0d\Article 73 The content of food advertisements shall be true and legal, shall not contain false content, and shall not involve disease prevention or treatment functions. Food producers and operators are responsible for the authenticity and legality of food advertising content. \x0d\The food and drug regulatory authorities and other relevant departments of the people's governments at or above the county level, as well as food inspection agencies and food industry associations, are not allowed to recommend foods to consumers in advertisements or other forms. Consumer organizations may not recommend food to consumers by charging fees or seeking other benefits. \x0d\Section 4 Special Foods\x0d\Article 74 The state implements strict supervision and management of special foods such as health foods, formula foods for special medical purposes, and formula foods for infants and young children. \x0d\Article 75 Health food claims for health functions shall have scientific basis and shall not cause acute, subacute or chronic harm to the human body. \x0d\The catalog of health food raw materials and the catalog of health functions allowed for health food claims shall be formulated, adjusted and published by the Food and Drug Administration Department of the State Council in conjunction with the Health Administration Department of the State Council and the National Administration of Traditional Chinese Medicine. \x0d\The catalog of health food raw materials should include the name, dosage and corresponding effects of the raw materials; raw materials included in the catalog of health food raw materials can only be used in the production of health food and not in the production of other foods. \x0d\Article 76 Health foods that use raw materials other than those listed in the health food raw material catalog and health foods that are imported for the first time must be registered with the Food and Drug Administration Department of the State Council. However, if the health food imported for the first time contains nutritional supplements such as vitamins and minerals, it must be reported to the Food and Drug Administration of the State Council for filing. Other health foods should be reported to the food and drug supervision and administration department of the people's government of the province, autonomous region, or municipality directly under the Central Government for filing. \x0d\Imported health foods should be products approved for sale by the competent authorities of the exporting country (region). \x0d\Article 77 For health foods that should be registered in accordance with the law, the research and development report, product formula, production process, safety and health function evaluation, labels, instructions and other materials and samples of the health food must be submitted when registering, and relevant certificates must be provided document.

The food and drug administration department of the State Council will organize a technical review and approve the registration if it meets the requirements for safety and functional claims; if it does not meet the requirements, it will deny registration and explain the reasons in writing. If a decision is made to approve the registration of a health food using raw materials that are not included in the health food raw material catalog, the raw materials should be included in the health food raw material catalog in a timely manner. \x0d\For health foods that should be filed according to law, the product formula, production process, label, instructions and materials showing the product safety and health functions must be submitted when filing. \x0d\Article 78 The labels and instructions of health food shall not involve disease prevention and treatment functions. The content shall be true, consistent with the registered or filed content, and state the suitable groups, unsuitable groups, functional ingredients or iconic ingredients. and its content, etc., and state that "this product cannot replace drugs." The functions and ingredients of health food should be consistent with the labels and instructions. \x0d\Article 79 Health food advertisements, in addition to complying with the provisions of Paragraph 1 of Article 73 of this Law, must also state that "this product cannot replace drugs"; its content must be approved by the province, autonomous region, or autonomous region where the production enterprise is located. The food and drug supervision and administration department of the municipal people's government shall review and approve it and obtain the health food advertising approval document. The food and drug regulatory authorities of the people's governments of provinces, autonomous regions, and municipalities directly under the Central Government shall publish and promptly update the approved health food advertising catalog and approved advertising content. \x0d\Article 80 Formula foods for special medical purposes shall be registered with the Food and Drug Administration Department of the State Council. When registering, product formulas, production processes, labels, instructions, and materials showing product safety, nutritional adequacy, and clinical effects for special medical purposes should be submitted. \x0d\Advertising of formula foods for special medical purposes shall be subject to the Advertising Law of the People's Republic of China and other laws and administrative regulations on drug advertising management. \x0d\Article 81 Infant formula food manufacturers shall implement full-process quality control from raw materials entering the factory to finished products leaving the factory, and conduct batch-by-batch inspection of infant formula foods leaving the factory to ensure food safety. \x0d\ Raw milk, auxiliary materials and other food raw materials, food additives, etc. used in the production of infant formula foods must comply with the provisions of laws, administrative regulations and national food safety standards to ensure the nutrients required for the growth and development of infants and young children. \x0d\Infant formula food manufacturers shall file food raw materials, food additives, product formulas and labels with the food and drug supervision and administration departments of the people's governments of provinces, autonomous regions, and municipalities directly under the Central Government. \x0d\The product formula of infant formula milk powder shall be registered with the Food and Drug Administration Department of the State Council. When registering, a formula research and development report and other materials showing the scientific nature and safety of the formula should be submitted. \x0d\ Infant formula milk powder is not allowed to be produced in separate packages, and the same enterprise is not allowed to use the same formula to produce infant formula milk powder of different brands. \x0d\Article 82 The registrant or recorder of health food, formula food for special medical purposes, and infant formula milk powder shall be responsible for the authenticity of the materials submitted. \x0d\The food and drug regulatory authorities of the people's governments at or above the provincial level shall promptly publish the catalogs of registered or filed health foods, formula foods for special medical purposes, and infant formula milk powder, and keep confidential the business secrets of enterprises learned during registration or filing. \x0d\ Health food, formula foods for special medical purposes, and infant formula milk powder manufacturers shall organize production in accordance with registered or filed product formulas, production processes and other technical requirements. \x0d\Article 83 Enterprises that produce health foods, formula foods for special medical purposes, formula foods for infants and young children, and other main and supplementary foods for specific groups of people shall establish production facilities suitable for the foods they produce in accordance with the requirements of good production practices. Production quality management system, regularly conduct self-examination of the operation of the system to ensure its effective operation, and submit a self-examination report to the food and drug supervision and administration department of the local county-level people's government. \x0d\Above!