George A. Breon & Co. v. United States

74 F.2d 4, 1934 U.S. App. LEXIS 3854
CourtCourt of Appeals for the Eighth Circuit
DecidedNovember 19, 1934
DocketNo. 10046
StatusPublished
Cited by6 cases

This text of 74 F.2d 4 (George A. Breon & Co. v. United States) is published on Counsel Stack Legal Research, covering Court of Appeals for the Eighth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
George A. Breon & Co. v. United States, 74 F.2d 4, 1934 U.S. App. LEXIS 3854 (8th Cir. 1934).

Opinion

GARDNER, Circuit Judge.

This is an appeal from the judgment of the lower court finding appellant guilty upon the second count of an information charging it with having shipped in interstate commerce a bottle containing one hundred capsules, labeled one-quarter grain dessieated thyroid, and charging that the same was misbranded under the Food and Drug Act (title 21 US. CA §§ 1 to 25), in that said capsules contained more than one-quarter grain dessieated thyroid.

We shall refer to the appellant as defendant.

The information contained four counts. Trial by jury was waived, and the court, at [5]*5the conclusion of the evidence, found the defendant not guilty on counts 1, 3, and 4, but found it guilty on count 2. Defendant interposed a demurrer to count 2, on the ground that, unless the contents of the capsules fell below the indicated strength and purity, it was not a violation to ship them. The court overruled the demurrer, and also overruled defendant’s demurrer to the evidence as to this count.

On this appeal it is contended: (1) That the court erred in overruling the demurrer to count 2 of the information; (2) that the evidence is insufficient to warrant a conviction; and (3) that the verdict is against the declaration of law given by the trial court.

It is earnestly urged by defendant that furnishing an excess of the identical drug stated on the label, the drug being a harmless and wholesome one, is not a crime, and that the Pure Food and Drug Act was intended to protect public health and prevent fraud, and hence does not apply to a ease where health is not endangered and no fraud is committed. The government, on the other hand, contends that the act was passed for the purpose of protecting the general public, to preserve their health, and to prevent their being deceived by label or fraud as to the real character of the article offered for sale, and that, where drugs are involved, the act requires a correct statement on the label.

Section 9 of title 21 USCA provides: “The term ‘misbranded,’ as used in sections 1 to 35, inclusive, of this title, shall apply to all drugs, or articles of food, or articles which enter into the composition of food, the package or label of which shall bear any statement, design, or device regarding such article, or the ingredients or substances contained therein which shall be false or misleading in any particular, and to any food or drug product which is falsely branded as to the State, Territory, or country in which it is manufactured.”

Section 10 of title 21 USCA provides in part as follows:

“For the purposes of sections 1 to 15, inclusive, of this title, an article shall be deemed to be misbranded;
“Drugs. In case of drugs:
“Imitation or Use of Name of Other Article. — First. If it be an imitation of or offered for sale under the name of another article.
“Removal and Substitution of Contents of Package, or Failure to Stale on Label Quantity or Proportion of Narcotics Therein. — ■ Second. If the contents of the package as originally put up shall have been removed, in whole or in part, and other contents shall have been placed in such package, or if the package fail to bear a statement on the label of the quantity or proportion of any alcohol, morphine, opium, cocaine, heroin, alpha or beta eucaine, chloroform, cannabis indica, chloral hydrate, or acetanilide, or any derivative or preparation of any such substances contained therein.
“False Statement of Curative or Therapeutic Effect. — Third. If its package or label shall bear or contain any statement, design, or device regarding the curative or therapeutic effect of such article or any of the ingredients or substances contained therein, which is false and fraudulent.”

It appears from the evidence in this case that the drug involved is not a potent, poisonous, or harmful one, and that no harm would result to a person from taking capsules containing approximately one-third of a grain of thyroid, instead of a capsule containing one-quarter of a grain of thyroid, nor, indeed, from the taking of a series of bottles of such capsules. This is not a case in which the defendant is charged with adulteration, but with misbranding, and the falsity of the label is not as to the ingredients or substances contained in the capsules, but as to the quantity contained therein. The government contends that the label is false and misleading within the meaning of section 9, title 21, supra, and that it is not material that the drug was a harmless and wholesome one, nor that the label understated the amount of such drug. It is persuasively argued by defendant that the added strength or quantity of thyroid could not have been within the purpose of this statute, and that the statute was aimed at the giving of a less amount, rather than an excess, and by way of illustration it is said in counsel’s brief: “If I sell a package of butter which is labeled ‘Pure Creamery Butter, net weight 1 Lb.,’ it is necessary to determine the strength, quality and purity of the butter fat and other articles contained in this substance, in order to determine whether or not it is the identical thing stated, namely, pure creamery butter, but if it is pure creamery butter, and I sell in the package 18 ounces of the pure creamery butter instead of the one pound net weight declared on the label, there is no misbranding, because I have sold the identical thing or substance which the label declared. I have merely given the purchaser good measure, and I have violated no law.”

[6]*6In the view we have taken of the other issues involved, however, we do not deem it necessary to pass upon this question.

At the request of defendant, the court gave the following declaration of law: “The court declares the law to he that the burden is upon the Government to show beyond a reasonable doubt that the Thyroid mentioned in Counts One and Two, contained more than *4 grain of Thyroid, and in such quantity as not to permit a reasonable tolerance or variance, and if the court finds and believes from the evidence that the assay made by the Government chemists under the supervision of the Secretary of Agriculture, was not correct, or if there is a reasonable doubt as to the accuracy of such assay, if any, then the Court-should find the defendant not guilty as charged in the First and Second Counts of the information.”

The United States Pharmacopoeia prescribes a method for determining the iodine content of powdered thyroid. It also states that: “Thyroid contains not less than 0.17 and not more than 0.23 per cent of iodine in thyroid combination, and must be free from iodine in inorganic or any other form of combination than that peculiar to the thyroid gland.” The capsules in question contained, in addition to thyroid, calcium, phosphate, carbonate, and starch. One of the government’s experts testified that, using the method of analysis prescribed by the United States Pharmacopoeia, he obtained a 53> per cent, excess in an analysis of 30 of the one-quarter grain capsules. On analyzing ten more, the result was within 3 per cent, of the first analysis. Another of the government’s experts testified that, using twenty of the quarter-grain capsules, he found a 42 per cent, excess.

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Bluebook (online)
74 F.2d 4, 1934 U.S. App. LEXIS 3854, Counsel Stack Legal Research, https://law.counselstack.com/opinion/george-a-breon-co-v-united-states-ca8-1934.