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[海外资讯]美国食品药品监督管理局就食品标签法规征求公众意见

来源:中国豆制品网      2014/1/22 10:10:58      点击:

  食品伙伴网讯  据联邦公报消息,2013年12月30日美国食品药品监督管理局就食品标签法规征求公众意见,截止日期为2014年1月29日。

   部分原文报道如下:

   Our food labeling regulations require food producers to disclose to consumers and others specific information about themselves or their products on the label or labeling of their products. Related regulations require that food producers retain records establishing the basis for the information contained in the label or labeling of their products and provide those records to regulatory officials. Finally, certain regulations provide for the submission of food labeling petitions to us. We issued our food labeling regulations under parts 101, 102, 104, and 105 (21 CFR parts 101, 102, 104, and 105) under the authority of sections 4, 5, and 6 of the Fair Packaging and Labeling Act (FPLA) (15 U.S.C. 1453, 1454, and 1455) and sections 201, 301, 402, 403, 409, 411, 701, and 721 of the Federal Food, Drug, and Cosmetic Act (FD Act) (21 U.S.C. 321, 331, 342, 343, 348, 350, 371, and 379e)。 Most of these regulations derive from section 403 of the FD Act, which provides that a food product shall be deemed to be misbranded if, among other things, its label or labeling fails to bear certain required information concerning the food product, is false or misleading in any particular, or bears certain types of unauthorized claims. The disclosure requirements and other collections of information in the regulations in parts 101, 102, 104, and 105 are necessary to ensure that food products produced or sold in the United States are in compliance with the labeling provisions of the FD Act and FPLA.

   Upon review of the information collection requests supporting these food labeling regulations, FDA found that the third-party disclosure burdens associated with the requirements found in §§ 101.9(c)(2)(ii) and 101.36(b)(2) todeclare the amount of trans fatty acids present in a food, and with the voluntary declaration of the quantitative amount and the percent of Daily Value of a dietary ingredient on a "per day" basis in addition to the required "per serving" basis are in use without current OMB approval. These collections of information were previously approved by OMB under control numbers 0910-0595 and 0910-0395 respectively; however, the approval period for these collections has expired. To remedy this oversight, to most appropriately streamline these information collections, and to eliminate redundancy in its information collection requests, we seek to revise the instant collection to include these third-party disclosure elements and have included them in the burden estimates and discussion in this document in support of our approval request for OMB control number 0910-0381.      

   原文链接:https://www.federalregister.gov/articles/2013/12/30/2013-31215/agency-information-collection-activities-submission-for-office-of-management-and-budget-review