Name and place of business of the manufacturer, packer, or distributor.The information on the product must include: The purpose of the Uniform Packaging and Labeling Regulation (UPLR) is to provide adequate information on product labels so that consumers and businesses can make price and quantity comparisons. Book a free consultation call today with Ivan Malloci to learn how we can help you with:īOOK A FREE CONSULTATION What is the Uniform Packaging and Labeling Regulation (UPLR)?.So even if a product is exempt under the UPLR, it could still be required to fulfill compliance obligations under state law.We Help Brands & Importers With Product Compliance (US & EU) In the United States, all 50 states have their own type of packaging and labeling regulations in effect for consumer products that lay out separate packaging and labeling requirements based on the state’s laws. As with the FPLA, the UPLR also aims to ensure that consumers are provided accurate and adequate information about the identity and quantity of contents in any product they might purchase. It contains laws and regulations governing Legal Metrology and Engine Fuel Quality, NIST Handbook 130, and has been adopted into law in 45 out of 50 U.S. The Uniform Packaging and Labeling Regulation (UPLR) was first adopted at the 37th National Conference on Weights and Measures in 1952. However, it does set out labeling regulations for the same, even though these products can be subject to other labeling regulations set out by other state- or federal-level regulatory authorities as well. In particular, the FPLA determines labeling compliance for goods or commodities on the basis of weight or measure.Īlso, FPLA does not oversee compliance for consumer products, such as food, meat, poultry, tobacco, drugs, medical devices, or cosmetics, etc. Labeling requirements cover the contents, identity, and name and place of business of the product’s manufacturer, packer, or distributor, among other compliance aspects. different federal- and state-level agencies formulate and enforce a gamut of product category-specific labeling regulations.Įnacted in 1967, the Fair Packaging and Labeling Act (FPLA) of the United States allows the Federal Trade Commission and the Food and Drug Administration to formulate and enforce regulations governing the labeling of all consumer commodities. Products that are imported into the United States are expected to comply with Title 19, United States Code, Chapter 4, Section 1304 and 19 CFR 134, Country of Origin Marking regulations.īased on product categories, such as electronics, food, medical devices, etc. In the United States, labeling requirements for a product need to be compliant with the Fair Packaging and Labeling Act (FPLA) and the Uniform Packaging and Labeling Regulation (UPLR). Beginning from how the idea to create or manufacture a product, to the process of manufacturing the product, to its packaging and labeling, and finally, to where and how it is sold in the marketplace, a complex framework of compliance regulations is used to maintain oversight for this entire procedure beginning from say the factory floor to when the product is on a store shelf. Before a product is ready to be sold in the marketplace, it needs to undergo a comprehensive evaluation from a compliance perspective.
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