§ 2110. Rule of construction

421 words·~2 min read·/usc/title-21/section-2110

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

Nothing in this chapter (or an amendment made by this chapter) shall be construed to affect—

(1)the regulation of dietary supplements under the Dietary Supplement Health and Education Act of 1994 (Public Law 103–417); or

(2)the adverse event reporting system for dietary supplements created under the Dietary Supplement and Nonprescription Drug Consumer Protection Act (Public Law 109–462).

(Pub. L. 110–85, title X, § 1011, Sept. 27, 2007, 121 Stat. 971.)

Connections2 cite this · traces to 4

Cited by 2 sections · top 1

statutes-at-large

Public Law 110–85
To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and for medical devices, to enhance the postmarket authorities of the Food and Drug Administration with respect to the safety of drugs, and for other purposes

Traces to 4 documents

U.S. Code

12 references not yet in our index

Public Law 103–417
Public Law 109–462
Pub. L. 110–85, title X, § 1011
121 Stat. 971
Pub. L. 110–85
121 Stat. 962
Pub. L. 103–417
108 Stat. 4325
Pub. L. 109–462
120 Stat. 3469
Pub. L. 110–85, title X, § 1005(g)
121 Stat. 969

Citation graph

cites case law

§ 2110

Rule of construction

Stat.×2

Pub. L.Public Law 103–417

Pub. L.Public Law 109–462

Pub. L.Pub. L. 110–85, title X, § 1011

Stat.121 Stat. 971

Pub. L.Pub. L. 110–85

Cites 16 · showing 9Cited by 2 across 1 source