Regulations for application and reviewing of nutritional
Regulations for Application and Evaluation of Nutritional Supplement (interim) Article 1 For standardizing the evaluation of nutritional supplement, the regulations are formulated in
accordance with Food Assanation of the People’s Republic of China and Provisions for Health Food
Article 2 Nutritional supplement refers to those products which can supply vitamin, minerals rather than
providing energy. The function is to supplement any deficiency in nutrition intake from diet, prevent nutrition
deficiency and reduce the danger of chronically degenerative diseases.
Article 3 Nutritional supplement shall be in accordance with the following requirements:
Nutritional supplement is limited to supplement vitamin and minerals. The kinds of vitamin and
minerals shall meet the Kind and Dosage of Vitamin and Minerals.
The raw material of Nutritional supplement comes from the Article, which is in the List of Vitamin
The purpose of the adjuvant is just satisfying with the requests of product artwork or improves the
color, perfume, and the taste of the product. Moreover it shall conform to the proportional national
If the suitable crowd is adult, the recommended everyday intake of the vitamin, minerals should
conform to regulations of the Kind and Dosage of Vitamin and Minerals. If the suitable crowd is
pregnant woman, wet nurse and the crowd under 18 years old, the recommended everyday intake of
the vitamin, mineral matter should be controlled in the 1/3～2/3 level of the recommended intake（RNIs or AIs）, which accords with those people in our country.
The ingested total amount of the product should be smaller, which is recommended. The main form
of the product is tablets、collocystis、drug granules or the liquid by taking orally. The everyday edible
dosage of the drug granules shouldn’t exceed 20 gram. The everyday edible dosage of the liquid by
taking orally shouldn’t exceed 30 milliliter.
Article 4 If the Article that has been used is in the List of Vitamin and Chemical Compound in Minerals,
generally the test report in safe toxicology cannot be supplied with. Because its product material, artwork and
quality standard accords of the national relevant regulations. If the Article that have been used is outside the
List of Vitamin and Chemical Compound in Minerals, the documents should be provided, which includes of
the effect in nutriology of material, the science records of metabolic process and safe intake in vivo, together
with the report of evaluation test in safe toxicology which is showed by relevant request according to the safe
Article 5 The applicant should provide the quantitation test method of nutrients in nutritional supplement. Article 6 The signal value of nutritional supplement indicates that the product labeling and the definite figure
of some nutrients content, which is showed in the directions, but cannot be labeled the scope value.
The signal value of nutritional supplement and the scope value of nutrients content in product quality criteria
should be consistent with the relevant regulation ,which is in mentioned the third and forth regulation.
Article7 The multivitamins or mineral supplement should be vitamins above three kinds or nutritional Article 8 The product should be adopted commitment pack, which is easily edible for consumer and
maintains product stability. The packing material must accord with the regulation of the relevant hygienic
guide or sanitary requirement, which directly contacts with nutritional supplement.
Article 9 The label of nutrients nutritional supplement, directions should be in accord with the relevant
regulation of nation, meanwhile should indicate the following contents:
The word of “nutritional supplement”.
The nutritional ingredient should be labeled with the smallest edible unit of nutrients content.
The edible method and dosage should have the concretely recommended intake of different crowd.
Announcements: the product shouldn’t be instead of medicine, cannot exceed the recommended
intake or eats them together with the congener nutritional supplement.
Article 10 The State Food and Drug Administration (SFDA) institutes and issues the Kind and Dosage of
Vitamin and Minerals, the List of Vitamin and Chemical Compound in Minerals.
Article 11 The State Food and Drug Administration (SFDA) take responsibility to interpret the regulations. Article 12 The regulations shall go into effect as of July 1, 2005. The issued regulations, if not in accordance
with this one, should conform to this one.
Table 1: the Kind and Dosage of Vitamin and Minerals
Table 2: the List of Vitamin and Chemical Compound in Minerals
The Kind and Dosage of Vitamin and Minerals
retinol equivalent(vitamin A or vitamin A adds 250μgRE/d
The List of Vitamin and Chemical Compound in Minerals
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