Opinion · Supreme Court of the United States

McDermott v. Wisconsin

228 U.S. 115

Type
Opinion
Court
Supreme Court of the United States
Jurisdiction
Federal
Date
1913-04-07
Topic
general

How later courts describe this case

  • upholding federal regulation over labelling requirements for goods travelling through interstate commerce
  • Federal act permitting certain labelling preempts contrary state provision preventing use of federally approved labelling.
  • “no longer open to question” that Congress has full and ample power to regulate food and drugs
  • construing Food and Drugs Act of 1906, 34 Stat. 768
  • invalidating state law directly conflicting with federal regulations

Citator

UpLaw has not yet analyzed McDermott v. Wisconsin. The absence of a flag is not a finding that it is good law.

Cited by
145 opinions

Headnotes

  1. Constitutional Law — Commerce Power Congress has not only the right to pass laws regulating legitimate commerce among the States and with foreign nations, but also full power to bar from the channels of such commerce illicit or harmful articles, and to make articles injurious to the public health outlaws of interstate commerce; Congress may itself determine the means appropriate to that purpose, and, so long as they do no violence to other provisions of the Constitution, Congress is the judge of the means to be employed in exercising that power. 228 U.S. 115, 128 (1913)
  2. Healthcare Law — Statutory Construction The Pure Food and Drugs Act was passed under Congress's authority to exclude impure and adulterated food and drugs from interstate commerce and to prevent the facilities of such commerce from being used to transport such articles from their place of manufacture to the people who consume them, and the Act must be construed in the light of that purpose and of the power exerted by Congress in its passage. 228 U.S. 115, 128 (1913)
  3. Healthcare Law — Prohibited Articles The articles of food or drugs whose shipment or delivery for shipment in interstate commerce is prohibited and punished by § 2 of the Food and Drugs Act are those which are adulterated or misbranded within the meaning of the Act, as adulteration and misbranding are defined in the Act's other provisions. 228 U.S. 115, 129 (1913)
  4. Healthcare Law — Meaning of "Package" The word "package," or its equivalent, as used in §§ 7 and 8 of the Food and Drugs Act in defining adulteration and misbranding refers to the immediate container of the article which is intended for consumption by the public; to limit the requirements of the Act to the outside wrapping or box not seen by the purchasing public would render the Act nugatory and its provisions inadequate to accomplish the purposes for which it was passed. 228 U.S. 115, 130 (1913)
  5. Constitutional Law — Federal Supremacy While enactment of the Food and Drugs Act does not prevent a State from making regulations, not in conflict therewith, to protect its people against fraud or imposition by impure food and drugs, a State may not, under the guise of exercising its police power or otherwise, impose burdens upon or discriminate against interstate commerce, nor enact legislation in conflict with the statutes of Congress on the subject; to the extent a state law interferes with or frustrates the operation of an act of Congress, its provisions must yield to the superior Federal power. 228 U.S. 115, 131-132 (1913)
  6. Healthcare Law — Enforcement Authority Whether articles in interstate commerce have been labeled in compliance with the Food and Drugs Act is not for the State to determine, but is a matter provided for by the Act of Congress and to be determined as therein indicated by proper proceedings in the Federal courts. 228 U.S. 115, 132 (1913)
  7. Constitutional Law — Commerce Clause As the Federal Food and Drugs Act requires articles in interstate commerce to be properly labeled, a State cannot require a label properly affixed under that statute to be removed and other labels authorized by its own statute to be affixed to the package containing the article, so long as the article remains unsold by the importer, whether or not it remains in the original case; such a requirement is beyond the power of the State. 228 U.S. 115, 132-133 (1913)
  8. Constitutional Law — Original Package Doctrine The doctrine of original packages was not intended to limit the right of Congress, when it chooses to assert it, to keep the channels of interstate commerce free from the carriage of injurious or fraudulently branded articles and to choose appropriate means to that end; legislative means provided in a Federal statute for its own enforcement may not be thwarted by state legislation having the direct effect of impairing the effectual exercise of such means. 228 U.S. 115, 137 (1913)
  9. Healthcare Law — Seizure of Misbranded Articles Where Congress has made adulterated and misbranded articles contraband of interstate commerce, it may provide for their seizure and condemnation under § 10 of the Food and Drugs Act not only while they are being transported in interstate commerce but also after transportation, while the goods remain "unloaded, unsold, or in original unbroken packages"; the Act reaches the goods provided they are unsold, whether or not they remain in original packages, and such provisions are within the power of Congress as measures essential to accomplishing the purpose of the Act. 228 U.S. 115, 136-137 (1913)
  10. Constitutional Law — Invalidity of Wisconsin Statute A Wisconsin statute of 1907 prescribing an exclusive label for syrup mixtures and forbidding all other labels is invalid so far as it relates to articles properly branded on the immediate container under the Federal Food and Drugs Act and brought into the State in interstate commerce, so long as they remain unsold by the importer, whether or not they remain in the original outside package. 228 U.S. 115, 137 (1913)