Fair Packaging and Labeling Act definition

Fair Packaging and Labeling Act means the Fair Packaging and Labeling Act as it relates to foods and cosmetics, 15 U.S.C. secs. 1451 et seq., and all amendments thereto;
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Fair Packaging and Labeling Act means the Fair Packaging and Labeling Act as it
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Examples of Fair Packaging and Labeling Act in a sentence

  • Since its inception, the Uniform Packaging and Labeling Regulation has been continually revised to meet the complexities of an enormous expansion in the packaging industry – an expansion that, in late 1966, brought about the passage of the Fair Packaging and Labeling Act (FPLA).

  • Each package shall be identified with manufacturer's label, which shall conform to the requirements of the Fair Packaging and Labeling Act and Section 12604 of the California Business and Professions Code.

  • No label, con- tainer, or packaging material bearing official identification may be printed or prepared for use until the printers’ or other final proof has been approved by the Administrator in accordance with the regulations in this part, the Federal Food, Drug, and Cosmetic Act, the Fair Packaging and Labeling Act, and the regulations promulgated under these acts.

  • Each package shall be identified with manufacturer's label, which shall conform to the requirements of the Fair Packaging and Labeling Act of the California Business and Professions Code Section 12601-12615.5.

  • This subchapter shall be known and be cited as the "Maine Fair Packaging and Labeling Act." [PL 1969, c.

  • In 1992, Congress amended the Federal Fair Packaging and Labeling Act to require certain consumer commodities to include the appropriate SI units along with the U.S. customary units in their quantity statements.(Added 1993) (Revised 2008 and 2019) K.

  • Nutrition in-formation must be included on the la- beling of each unit container of con- sumer packaged shell eggs in accord- ance with the provisions of title 21, chapter I, part 101, Regulations for the Enforcement of the Federal Food, Drug, and Cosmetic Act and the Fair Packaging and Labeling Act.

  • For complete classification of this Act to the Code, see section 301 of this title and Tables.The Fair Packaging and Labeling Act, referred to in subsecs.

  • The only proposed amendment to the bill, which would have exempted whiskey, a kind of distilled spirit, from the food mis- branding provision of the FD&C Act, but not from the FAA Act was deleted by the conference committee.37 Also, unlike the Fair Packaging and Labeling Act which adopts the FD&C Act definition of “food” and then expressly exempts beverages from complying with the FAA Act as listed in 15 U.S.C. section 1459(a)(4), the FD&C Act contains no such qualification.

  • The Food and Drug Administration (FDA) regulates food, drugs, cosmetic products, and medical devices under the Food, Drug, and Cosmetic Act (FDCA) and the Fair Packaging and Labeling Act (FPLA).

Related to Fair Packaging and Labeling Act

  • health and safety specification means a site, activity or project specific document prepared by the client pertaining to all health and safety requirements related to construction work;

  • HITECH Act means the Health Information Technology for Economic and Clinical Health Act, TitleXIII, Subtitle D, Part 1 & 2 of the American Recovery and Reinvestment Act of 2009.

  • PPACA means the federal Patient Protection and Affordable Care Act (Public Law 111-148), as amended by the federal Health Care and Education Reconciliation Act of 2010 (Public Law 111-152), and any rules, regulations, or guidance issued thereunder.

  • cGMP means current Good Manufacturing Practices as specified in the United States Code of Federal Regulations, ICH Guideline Q7A, or equivalent laws, rules, or regulations of an applicable Regulatory Authority at the time of manufacture.

  • Accessibility Standards means accessibility standards and specifications for Texas agency and institution of higher education websites and EIR set forth in 1 TAC Chapter 206 and/or Chapter 213.

  • health and safety file means a file, or other record containing the information in writing required by these Regulations "health and safety plan" means a site, activity or project specific documented plan in accordance with the client's health and safety specification;

  • Federal safety requirements means applicable provisions of 49 U.S.C. § 30101 et seq. and all

  • Data Protection Laws and Regulations means all laws and regulations, including laws and regulations of the European Union, the European Economic Area and their member states, Switzerland and the United Kingdom, applicable to the Processing of Personal Data under the Agreement.