Fair Packaging and Labeling Act definition
Examples of Fair Packaging and Labeling Act in a sentence
Without limitation of the foregoing, Vendor shall ensure the Products and any related packaging of the Products conform fully to, any applicable law, including, without limitation, the Federal Food and Cosmetic Act, the Fair Packaging and Labeling Act, The Federal Trade Commission Act, Poison Prevention Packaging Act, Occupational Health and Safety Act and California’s Prop 65 Act (so as to avoid adding a Proposition 65 warning label on the Products).
HHS-FDA is responsible for implementing and enforcing the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301, et seq.), the Public Health Service Act (42 U.S.C. 201, et seq.), and the Fair Packaging and Labeling Act (15 U.S.C. 1451 et seq.).
All product (except fresh fruit and vegetables) must be labeled per the Fair Packaging and Labeling Act.
Require that all of the information that is required by the Food, Drug, and Cosmetic Act and the Fair Packaging and Labeling Act of the United States is included on the packaging of individual products.
Distributor expressly recognizes and understands that said Professional Use Only Products are not or may not be labeled in conformity with the provisions of and regulations promulgated pursuant to the Fair Packaging and Labeling Act and that sale of these Professional Use Only Products to the consuming public could violate both the Fair Packaging and Labeling Act and the Food, Drug and Cosmetic Act and is not permitted.
The purpose of this Arrangement is to leverage FDA’s and the VAP’s respective seafood safety systems to assure that shrimp exported from Ecuador to the United States are safe for human consumption, and meet applicable U.S. requirements, including relevant provisions of the U.S. Federal Food, Drug, and Cosmetic Act, the U.S. Public Health Service Act, the U.S. Fair Packaging and Labeling Act, and Title 21 of the U.S. Code of Federal Regulations.
All inventory to be transferred to Horizon will be merchantable, fit for its intended purpose and in full compliance with the Federal Food Drug and Cosmetic Act of 1938, as amended, the Federal Fair Packaging and Labeling Act of 1966, as amended ,and any other applicable federal, state or local food and drug, consumer safety or consumer protection law or regulation and will comply with all other applicable state and local laws and regulations.
Since January 1, 1999, none of the Products has been the subject of any voluntary or involuntary recall campaign performed by Sellers or any voluntary or involuntary recall campaign required by, or performed in cooperation with, any governmental agency, that would adversely affect the performance or quality of such Products and there are no claims or suits alleging violations of the Fair Packaging and Labeling Act.
In addition, Contractor specifically warrants and guarantees to the GBI and the State that the system and any system items, products, software and services provided under the Contract are in compliance with Sections 5 and 12 of the Federal Trade Commission Act; the Fair Packaging and Labeling Act; the Consumer Product Safety Act, the Federal Hazardous Substance Act, the Fair Labor Standards Act and the Anti-Kickback Act of 1986.
The United States Food and Drug Administration (FDA) is the competent authority for milk and milk products and is responsible for the enforcement of the Federal Food, Drug, and Cosmetic Act (hereinafter the FD&C Act) (21 U.S.C. 301, et seq.), the Public Health Service Act (42 U.S.C. 201, et seq.), and the Fair Packaging and Labeling Act (15 U.S.C. 1451, et seq.).