Constitutionality of Proposed Limitations on Tobacco Industry

Department of Justice Office of Legal Counsel·Decided May 13, 1998·Published

Opinion

Constitutionality of Proposed Limitations on Tobacco Industry Congress has the authority under the C onstitution to im pose significant new regulations on tobacco com panies, including (1) restrictions on advertising and m arketing o f tobacco products that are tailored to prevent access to advertising by m inors; (2) contingent m onetary exactions, to be col­ lected from tobacco com panies if tobacco use by m inors fails to meet prescribed targets; and (3) requirem ents that com panies disclose certain docum ents to the public and to federal regulators

Consent by the tobacco com panies to increased federal regulation, w hich those com panies m ight grant in order to qualify for federally prescribed lim its on liability, would perm it C ongress to establish additional restrictions on tobacco advertising that it could not im pose directly.

May 13, 1998

S t a t e m e n t B e f o r e t h e C o m m it t e e o n t h e J u d ic ia r y U n it e d St a t e s S e n a t e

Mr. Chairman, thank you for inviting the Department of Justice to testify regarding the constitutionality of limitations on the tobacco industry that are cur­ rently under consideration in the Senate. We begin by addressing Congress’s con­ stitutional authority to regulate the tobacco industry without that industry’s con­ sent. We will explain that, even in the absence of consent, the Congress may impose important restrictions on the tobacco industry in furtherance of the public health. Included among such permissible regulations are (1) meaningful restric­ tions on the advertising and marketing of tobacco products; (2) the direct imposi­ tion of “ lookback” assessments; and (3) document disclosure requirements. We address these particular categories because some have questioned Congress’s power in these areas. Finally, we address the benefits of obtaining industry con­ sent.

I. Congress Can Enact Comprehensive Tobacco Legislation Without the Industry's Consent

Last September, the President announced five principal goals for comprehensive tobacco legislation. Those goals include:

* a comprehensive plan to reduce teen smoking, including the imposition of assessments that would increase cigarette prices by amounts necessary to meet youth smoking targets;

* express reaffirmation that the Food and Drug Administration ( “ FDA” ) has full authority to regulate tobacco products;

* changes in the way the tobacco industry does business, espe­ cially in the area of advertising directed at children;

79 Opinions o f the Office o f Legal Counsel in Volume 22

* progress toward other critical public health goals, such as the expansion of smoking cessation and prevention programs and the reduction of secondhand smoke; and

* protection for tobacco farmers and their communities.

Certainly there would be significant advantages to having the tobacco industry participate in the nation’s effort to reduce youth smoking, hence the President has indicated that he would prefer the industry do so. But Congress has ample authority to enact comprehensive tobacco legislation that achieves these crucial goals without the industry’s consent.

For example, consistent with the Constitution, Congress may enact, without industry consent, provisions that would:

* impose assessments on all tobacco manufacturers that would increase the price of cigarettes by $1.10 per pack over five years;

* confirm full FDA authority;

* establish marketing and advertising restrictions that would track the FDA’s regulation;

* impose extensive labelling and ingredient disclosure require­ ments;

* fund programs that would protect tobacco farmers and their communities;

* impose significant lookback assessments that would ensure continued reductions in youth smoking;

* establish licensing and registration provisions that would pre­ vent the creation of a black market; and

* require disclosure of relevant, non-privileged documents.

The Department believes that Congress can and should pass a law that achieves all of the above objectives, with or without the industry’s consent. Every day we delay, 3,000 more of our children take up smoking; at present rates, 1,000 of them will die prematurely as a result. Congress has the constitutional power to rewrite their future with a comprehensive tobacco bill.

80 Constitutionality o f Proposed Limitations on Tobacco Industry

II. Congress o r the FDA Can Impose Marketing Restrictions on the Tobacco Industry Without Its Consent

A. D irect Imposition o f the FDA Regulations

Under prevailing Supreme Court precedent, the government has the authority to impose restrictions on tobacco product advertising, where such restrictions are appropriately tailored to prevent access to advertising by minors, who may not lawfully purchase the advertised product. Thus, while there are certain advertising restrictions that may need industry consent in order to survive constitutional chal­ lenge, it is important not to lose sight of the important advertising restrictions— such as those set forth in the FDA regulation— that may be imposed directly. Under the test set out by the Supreme Court in Central Hudson Gas & Elec. Corp. v. Public Serv. C om m ’n, 447 U.S. 557 (1980), the threshold question is whether the regulated speech is “ related to unlawful activity” or is misleading. Id. at 564. If so, the speech can be freely regulated by the government. Because children cannot lawfully purchase tobacco products, Congress may restrict tobacco advertising that promotes those unlawful transactions. Tobacco advertising does, however, provide information to adults, who may lawfully purchase tobacco products. Thus, it is necessary to consider the remainder of the Central Hudson test in evaluating the constitutionality of restrictions on tobacco advertising. That test asks (1) “ whether the asserted governmental interest is substantial;” (2) “ whether the regulation directly advances the governmental interest asserted;” and (3) “ whether [the regulation] is not more extensive than is necessary to serve that interest.” Id. at 566. There is no question that the interest in protecting children from becoming addicted to tobacco products is substantial and that marketing restrictions such as those in the FDA’s regulation advance that interest. That leaves only the last part of the test—the “ fit.” This inquiry does not amount to a “ least restrictive means” test. Instead, the Supreme Court’s decisions require “ reasonable” fit between the government’s ends and the means chosen to accomplish those ends. See Board o f Trustees v. Fox, 492 U.S. 469, 480 (1989). The fit need not be perfect, only reasonable; it need not be the single best disposition, only one whose scope is in proportion to the interest served. See id. Accordingly, a commercial speech restriction will fail the narrow-tailoring requirement only if it “ burden[s] substantially more speech than necessary.” United States v. Edge Broad. Co., 509 U.S. 418, 430 (1993). Critically for present purposes, courts likely would find that a restriction is sufficiently tailored if it leaves open adequate alternative channels for the communication of commercial speech. See Florida Bar v. Went fo r It, Inc., 515 U.S. 618, 632 (1995). As we have argued in the pending litigation, the FDA’s regulation falls within the permissible scope of the government’s power.

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