21 C.F.R. 101.4 - Food; designation of ingredients

Cite as21 C.F.R. 101.4
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132 practice notes
  • Food for human consumption: Food labeling— Dietary supplements; effect on structure or function of body; types of statements, definition,
    • United States
    • Federal Register January 06, 2000
    • 6 Enero 2000
    ...In fact, FDA regulations require the ingredients in a dietary supplement to be listed on its label. (See Sec. 101.4(a)(1) and (g) (21 CFR 101.4(a)(1) and (g)), and Sec. 101.36). The rationale for Sec. 101.93(g)(2)(v) is that certain product class names (not particular ingredients) are so st......
  • Food Labeling: Revision of the Nutrition and Supplement Facts Labels
    • United States
    • Federal Register May 27, 2016
    • 27 Mayo 2016
    ...declaration that includes both types of sugars. In addition, although ingredients are listed in order of predominance by weight (21 CFR 101.4), the ingredient information is not a substitute for the gram amount of added sugars. An ingredient listing would not enable the consumer to understa......
  • In re Conagra Foods Inc., Case No. CV 11–05379 MMM (AGRx).
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Central District of California
    • 15 Noviembre 2012
    ...in any particular.” 21 U.S.C. § 343(a). The FDA has promulgated extensive regulations about the proper labeling of food. See, e.g., 21 C.F.R § 101.4 (designation of ingredients on food packaging); 21 C.F.R § 101.9 (labeling and advertising of nutrition information); 21 C.F.R § 101.13 (limit......
  • Gustavson v. Wrigley Sales Co., Case No.: 12–CV–01861–LHK
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Eastern District of California
    • 16 Septiembre 2013
    ...bars. FAC ¶ 148. According to the FAC, federal regulations require that ingredients be identified by their “common or usual name[s],” 21 C.F.R. § 101.4(a)(1), which the regulations state “shall accurately identify or describe, in as simple and direct terms as possible, the basic nature of t......
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81 cases
  • In re Conagra Foods Inc., Case No. CV 11–05379 MMM (AGRx).
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Central District of California
    • 15 Noviembre 2012
    ...in any particular.” 21 U.S.C. § 343(a). The FDA has promulgated extensive regulations about the proper labeling of food. See, e.g., 21 C.F.R § 101.4 (designation of ingredients on food packaging); 21 C.F.R § 101.9 (labeling and advertising of nutrition information); 21 C.F.R § 101.13 (limit......
  • Gustavson v. Wrigley Sales Co., Case No.: 12–CV–01861–LHK
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Eastern District of California
    • 16 Septiembre 2013
    ...bars. FAC ¶ 148. According to the FAC, federal regulations require that ingredients be identified by their “common or usual name[s],” 21 C.F.R. § 101.4(a)(1), which the regulations state “shall accurately identify or describe, in as simple and direct terms as possible, the basic nature of t......
  • Sciortino v. Pepsico, Inc., No. C–14–0478 EMC
    • United States
    • United States District Courts. 9th Circuit. United States District Courts. 9th Circuit. Northern District of California
    • 5 Junio 2015
    ...to warn). As discussed above, it has not done so.17 Defendant has cited two regulations purportedly governing warnings, (21 C.F.R. §§ 101.2, 101.4 ), yet these regulations appear to pertain to standards of identity under the NLEA.18 "We generally require a stay rather than a dismissal." R.R......
  • Jarrow Formulas, Inc. v. Nutrition Now, Inc., No. 01-55154.
    • United States
    • United States Courts of Appeals. United States Court of Appeals (9th Circuit)
    • 4 Junio 2002
    ...that its delay should be measured from 1999, when the FDA enacted regulations pertaining to the labeling of nutritional supplements, 21 C.F.R. §§ 101.4, 101.36. This argument is entirely without...
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21 firm's commentaries
  • FDA warns fresh fruit company, seasoning firm about serious violations
    • United States
    • LexBlog United States
    • 20 Enero 2020
    ...ingredients, but they do not bear labels that include a complete list of all the ingredients by common or usual name, as required by 21 CFR Part 101.4.” a.” Your Tugusto Chef Sazón con Culantro y Achiote product is manufactured using (redacted) however, it fails to list the sub-ingredients ......
  • The Revival Of ECJ Lawsuits: Sweet Tooth For Plaintiffs, Or Toothless Claims?
    • United States
    • Mondaq United States
    • 21 Junio 2017
    ...by pressing or diffusion, then clarified or evaporated"), (2) 21 C.F.R. 104(b)(20) (the common name for "sucrose" is "sugar"), (3) 21 C.F.R. 101.4(a)(1) (ingredients must be referred to by their common or usual name on food labels), (4) 21 C.F.R. 102.5(d) (the common or usual name of an ing......
  • The Revival of ECJ Lawsuits: Sweet Tooth For Plaintiffs, or Toothless Claims?
    • United States
    • JD Supra United States
    • 14 Junio 2017
    ...by pressing or diffusion, then clarified or evaporated”), (2) 21 C.F.R. 104(b)(20) (the common name for “sucrose” is “sugar”), (3) 21 C.F.R. 101.4(a)(1) (ingredients must be referred to by their common or usual name on food labels), (4) 21 C.F.R. 102.5(d) (the common or usual name of an ing......
  • FDA Guidance Regarding Structure-Function Claims for Dietary Supplements
    • United States
    • LexBlog United States
    • 12 Octubre 2009
    ...In fact, FDA regulations require the ingredients in a dietary supplement to be listed on its label. (See Sec. 101.4(a)(1) and (g) (21 CFR 101.4(a)(1) and (g)), and Sec. 101.36). The rationale for Sec. 101.93(g)(2)(v) is that certain product class names (not particular ingredients) are so st......
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