21 CFR 170.20 - General principles for evaluating the safety of food additives

Cite as21 CFR 170.20
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6 practice notes
  • Philip Morris Inc. v. Reilly, No. 00-2425
    • United States
    • United States Courts of Appeals. United States Court of Appeals (1st Circuit)
    • May 10, 2001
    ...as safe for use by the FDA and detailed on the labels of food products in order of predominance, see 21 U.S.C. §§ 342, 343, 348; 21 C.F.R. §§ 170.20-170.38, and drug products are subject to rigorous pre-market approval and must disclose on the label each active ingredient, see 21 U.S.C. §§ ......
  • Food for human consumption: Irradiation in production, processing, and handling of food— Ionizing radiation in treatment of food; x-ray maximum permitted energy level,
    • United States
    • Federal Register April 09, 2007
    • April 9, 2007
    ...(21 CFR 12.24(b)(2)). (5) Public Citizen asserts that by FDA failing to comply with Sec. 170.22, FDA did not comply with Sec. 170.20 (21 CFR 170.20), which states that ``the Commissioner will be guided by the principles and procedures for establishing the safety of food additives stated in ......
  • Irradiation in the Production, Processing, and Handling of Food
    • United States
    • Federal Register February 25, 2014
    • February 25, 2014
    ...various scientifically validated types of data may properly support a safety determination for a proposed use of a food additive (see 21 CFR 170.20(a)). Further, we have consistently taken the position that data obtained from specific foods irradiated under specific conditions may be extrap......
  • Red v. Gen. Mills, Inc., Case No. 2:15-cv-02232-ODW(JPR)
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Central District of California
    • December 29, 2015
    ...food additives and exempting foods that are generally recognized as safe. See Backus, 2015 WL 4932687, at *17; 21 U.S.C. §§ 342, 348; 21 C.F.R. § 170.20-170.38; 21 C.F.R. § 10.25(b) (the FDA "has primary jurisdiction to make the initial determination on issues within its statutory mandate")......
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2 cases
  • Philip Morris Inc. v. Reilly, No. 00-2425
    • United States
    • United States Courts of Appeals. United States Court of Appeals (1st Circuit)
    • May 10, 2001
    ...as safe for use by the FDA and detailed on the labels of food products in order of predominance, see 21 U.S.C. §§ 342, 343, 348; 21 C.F.R. §§ 170.20-170.38, and drug products are subject to rigorous pre-market approval and must disclose on the label each active ingredient, see 21 U.S.C. §§ ......
  • Red v. Gen. Mills, Inc., Case No. 2:15-cv-02232-ODW(JPR)
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Central District of California
    • December 29, 2015
    ...food additives and exempting foods that are generally recognized as safe. See Backus, 2015 WL 4932687, at *17; 21 U.S.C. §§ 342, 348; 21 C.F.R. § 170.20-170.38; 21 C.F.R. § 10.25(b) (the FDA "has primary jurisdiction to make the initial determination on issues within its statutory mand......

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