Pure Food and Drug Laws definition

Pure Food and Drug Laws means the FFDC Act and the pure food and drug laws of each of the states of the United States into which products of the Business, the Log Cabin Business and the Xxxxxx Xxxxx Business are or have been shipped.
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Pure Food and Drug Laws means (i) the Federal Food, Drug and Cosmetic Act, as amended from time to time, and any successor statute and (ii) the pure food and drug laws of each of the states of the United States into which products manufactured, marketed or sold by the Borrowers are or have been shipped.
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Examples of Pure Food and Drug Laws in a sentence

  • Company shall, and shall cause each of its Subsidiaries to, comply with the requirements of all applicable laws, rules, regulations and orders of any governmental authority (including all Pure Food and Drug Laws), noncompliance with which could reasonably be expected to cause a Material Adverse Effect.

  • Comply with requirements of all applicable laws, rules, regulations and orders of any Governmental Authority (including all Pure Food and Drug Laws), except to the extent that failure to comply herewith could not, in the aggregate, have a Material Adverse Effect (other than any non-compliance solely with respect to the ABA Pension Plan).

  • In addition, you agree to guarantee us against any loss occasioned by your failure to comply with any federal, state or other laws and regulations applying to the goods purchased under this order, and you further agree to compensate us for all damages suffered as a result of your failure to do so (e.g. Child Labor Act, Fair Labor Standards Act, Xxxxx-Xxxxx Act, Xxxxxxxx Xxxxxx Act, OPS Regulations, Pure Food and Drug Laws, etc.).

  • Lessee, its officers, employees, agents or servants shall, at all times, comply with the Federal Pure Food and Drug Laws, Health Rules and Regulations and other applicable Laws and Regulations of the United States Government, and the State of Colorado and all applicable Ordinances, Codes and Regulations of the City and County of Pueblo, including the rules and regulations governing the operation of the Airport.

  • Comply with requirements of all applicable laws, rules, regulations and orders of any Governmental Authority (including all Pure Food and Drug Laws), except to the extent that failure to comply herewith could not, in the aggregate, have a Material Adverse Effect.

Related to Pure Food and Drug Laws

  • Food and food ingredients means substances, whether in liquid, concentrated, solid, frozen, dried, or dehydrated form, that are sold for ingestion or chewing by humans and are consumed for their taste or nutritional value. Food and food ingredients do not include alcoholic beverages and tobacco.

  • FDCA shall have the meaning ascribed to such term in Section 3.1(hh).

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • New Drug Application means a new drug application in the United States for authorization to market a product, as defined in the applicable laws and regulations and submitted to the FDA.

  • Criminal drug statute means a Federal or non-Federal criminal statute involving the manufacture, distribution, dispensing, possession or use of any controlled substance.

  • Legend drug or "prescription drug" means any drug or device that has been determined to be unsafe for self- medication or any drug or device that bears or is required to bear the legend:

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • Legend drugs means any drugs which are required by state

  • FD&C Act means the United States Federal Food, Drug and Cosmetic Act, as amended.

  • FDA Laws means all applicable statutes (including the FDCA), rules and regulations implemented administered or enforced by the FDA (and any foreign equivalent).

  • Foreign Financial Regulatory Authority shall have the meaning given by Section 2(a)(50) of the 0000 Xxx.

  • Drug abuse means any pattern of pathological use of drugs that causes impairment in social or occupational functioning, or that produces physiological dependency evidenced by physical tolerance or by physical symptoms when it is withdrawn.

  • New drug means: (i) any drug, except a new animal drug or an animal feed bearing or containing

  • Drug addiction means a disease characterized by a

  • Biologics License Application or “BLA” means an application requesting permission from the FDA to introduce, or deliver for introduction, a biological product into interstate commerce, or any similar application or submission for marketing authorization of a product filed with a Regulatory Authority to obtain Regulatory Approval for such product in a country or group of countries.

  • Legal drug means any drug, including any prescription drug or over-the-counter drug, that has been legally obtained and that is not unlawfully sold or distributed.

  • foreign regulatory authority means a securities commission, exchange or other securities market regulatory authority in a designated foreign jurisdiction;

  • Governmental Regulations means all statutes, ordinances, rules and regulations of the Authorities applicable to Seller or the use or operation of the Real Property or the Improvements or any portion thereof.

  • MHLW means the Japanese Ministry of Health, Labour and Welfare, and any successor agency thereto.

  • Prescription drug order means an original or new order from a practitioner for drugs, drug-related devices or treatment for a human or animal, including orders issued through collaborative care agreements. Lawful prescriptions result from a valid practitioner-patient relationship, are intended to address a legitimate medical need, and fall within the prescribing practitioner's scope of professional practice;

  • Public health authority means an agency or authority of the United States, a state, a territory, a political subdivision of a state or territory, an Indian tribe, or a foreign government, or a person or entity acting under a grant of authority from or contract with such public agency, including the employees or agents of such public agency or its contractors or persons or entities to whom it has granted authority, that is responsible for public health matters as part of its official mandate.

  • FDA Act means the U.S. Federal Food, Drug, and Cosmetic Act, as amended.

  • Covered drug means any prescription drug that:

  • Health Canada means the section of the Canadian Government known as Health Canada and includes, among other departments, the Therapeutic Products Directorate and the Health Products and Food Branch Inspectorate;

  • Relevant Electric Retail Regulatory Authority means an entity that has jurisdiction over and establishes prices and policies for competition for providers of retail electric service to end- customers, such as the city council for a municipal utility, the governing board of a cooperative utility, the state public utility commission or any other such entity.

  • Invalid Drug Test means the result of a drug test for an oral fluid specimen that contains an unidentified adulterant, or an unidentified substance, that has abnormal physical characteristics, or that has an endogenous substance at an abnormal concentration preventing the laboratory from completing or obtaining a valid drug test result.