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§184.1979b 食品添加剂低矿物质乳清(Reduced minerals whey)

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放大字体  缩小字体 2011-07-29 09:41:55  来源:GPO  浏览次数:2664
核心提示:食品添加剂低矿物质乳清需达到的质量规格:蛋白质含量,10%~24%;脂肪含量,1%~4%;灰分含量最高7%;乳糖含量不超过85%;水分含量,1%~6%;固形物含量,视品种而定,按16.032中“总固体”方法I测定;可滴定酸度,视品种而定,按16.023中“牛乳”酸度(2)方法测定;杂质含量,以重金属(铅)计不超过10mg/kg;低矿物质乳清必须是从巴氏杀菌牛奶中提取,或者用于食品之前必须用巴氏杀菌方法处理过。低矿物质乳清用于食品中必须按照§184.1(b)(1)中现行良好生产操作规程。
发布单位
FDA
FDA
发布文号 64 FR 1761
发布日期 1999-01-12 生效日期 暂无
有效性状态 废止日期 暂无
备注 食品添加剂低矿物质乳清需达到的质量规格:蛋白质含量,10%~24%;脂肪含量,1%~4%;灰分含量最高7%;乳糖含量不超过85%;水分含量,1%~6%;固形物含量,视品种而定,按16.032中“总固体”方法I测定;可滴定酸度,视品种而定,按16.023中“牛乳”酸度(2)方法测定;杂质含量,以重金属(铅)计不超过10mg/kg;低矿物质乳清必须是从巴氏杀菌牛奶中提取,或者用于食品之前必须用巴氏杀菌方法处理过。低矿物质乳清用于食品中必须按照§184.1(b)(1)中现行良好生产操作规程。

    更多关于已证实属于一般公认为安全(GRAS)的可直接加入食品中的物质种类,请点击美国FDA 21 CFR 第184部分已证实属于一般公认为安全(GRAS)的可直接加入食品中的物质种类汇总

  § 184.1979b   Reduced minerals whey.

  (a) Reduced minerals whey is the substance obtained by the removal of a portion of the minerals from whey. The dry product shall not contain more than 7 percent ash. Reduced minerals whey is produced by physical separation techniques such as precipitation, filtration, or dialysis. As with whey, reduced minerals whey can be used as a fluid, concentrate, or a dry product form. The acidity of reduced minerals whey may be adjusted by the additional of safe and suitable pH-adjusting ingredients.

  (b) The reduced minerals whey meets the following specifications:

  (1) The analysis of reduced minerals whey, on a dry product basis, based on analytical methods in the referenced sections of “Official Methods of Analysis of the Association of Official Analytical Chemists,” 13th ed. (1980), which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51, is given in paragraphs (b)(1)(i) through (b)(1)(vii) of this section. Copies may be obtained from the AOAC INTERNATIONAL, 481 North Frederick Ave., suite 500, Gaithersburg, MD 20877, or may be examined at the Center for Food Safety and Applied Nutrition's Library, Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202–741–6030, or go to: http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.

  (i) Protein content, 10 to 24 percent—as determined by the methods prescribed in section 16.036 (liquid sample), entitled “Total Nitrogen—Official Final Action” under the heading “Total Solids,” or in section 16.193 (dry sample), entitled “Kjeldahl Method” under the heading “Protein—Official Final Action.”

  (ii) Fat content, 1 to 4 percent—as determined by the methods prescribed in section 16.059 (liquid sample), “Reese-Gottlieb Method [Reference Method] (11)—Official Final Action” under the heading “Fat,” or in section 16.199 (dry sample), entitled “Fat in Dried Milk (45)—Official Final Action.”

  (iii) Ash content, maximum 7 percent—as determined by the methods prescribed in section 16.035 (liquid sample), entitled “Ash (5)—Official Final Action” under the heading “Total Solids,” or in section 16.196 (dry sample), entitled “Ash—Official Final Action” under the heading “Dried Milk, Nonfat Dry Milk, and Malted Milk.”

  (iv) Lactose content, maximum 85 percent—as determined by the methods prescribed in section 16.057 (liquid sample), entitled “Gravimetric Method—Official Final Action” under the heading “Lactose,” or in section 31.061 (dry sample), entitled “Lane-Eynon General Volumetric Method” under the heading “Lactose—Chemical Methods—Official Final Action.”

  (v) Moisture content, 1 to 6 percent—as determined by the methods prescribed in section 16.192, entitled “Moisture (41)—Official Final Action” under the heading “Dried Milk, Nonfat Dry Milk, and Malted Milk.”

  (vi) Solids content, variable—as determined by the methods prescribed in section 16.032, entitled “Method I—Official Final Action” under the heading “Total Solid.”

  (vii) Titratable Acidity, variable—as determined by the methods prescribed in section 16.023, entitled “Acidity (2)—Official Final Action” under the heading “Milk,” or by an equivalent potentiometric method.

  (2) Limits of impurities are: Heavy metals (as lead). Not more than 10 parts per million (0.001 percent), as determined by the method described in the “Food Chemicals Codex,” 4th ed. (1996), pp. 760–761, which is incorporated by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies are available from the National Academy Press, Box 285, 2101 Constitution Ave. NW., Washington, DC 20055 (Internet address http://www.nap.edu ), or may be examined at the Center for Food Safety and Applied Nutrition's Library, Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202–741–6030, or go to: http://www.archives.gov/federal_register/code_of_federal_regulations/ibr_locations.html.

  (3) The reduced minerals whey shall be derived from milk that has been pasteurized, or the reduced minerals whey shall be subjected to pasteurization techniques or its equivalent before use in food.

  (c) The reduced minerals whey may be used in food in accordance with good manufacturing practice as indicated in §184.1(b)(1).

  (d) The percent of minerals present on a dry product basis, i.e., “reduced minerals whey (__% minerals),” shall be declared on the label of the package sold to food manufacturers. The percent of minerals may be declared in 2-percent increments expressed as a multiple of 2, not greater than the actual percentage of minerals in the product, or as an actual percentage provided that an analysis of the product on which the actual percentage is based is supplied to the food manufacturer.

  (e) The presence of reduced minerals whey in a finished food product shall be listed as “reduced minerals whey”。

  [46 FR 44441, Sept. 4, 1981, as amended at 54 FR 24899, June 12, 1989; 64 FR 1761, Jan. 12, 1999]

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