8751

Federal food drug and cosmetic act 21 u.s.c 321

Federal food drug and cosmetic act 21 u.s.c 321

[21 U.S.C. 301] This Act may be cited as the Federal Food, Drug, and Cosmetic Act. CHAPTER II—DEFINITIONS1 SEC. 201. [21 U.S.C. 321] For the purposes of this Act— 2 (a)(1) The term "State", except as used in the last sentence of section 702(a), means any State or Territory of the United States , the District of Columbia , and the."(1) as an admission that any product that is the subject of such notification violates any provision of the Federal Food, Drug, and Cosmetic Act (21 U.S Federal food drug and cosmetic act 21 u.s.c 321.C. 301 et seq.); or "(2) as evidence of an intention to promote or market the product for an indication or use for which the product has not been approved by the Secretary." Ex. Ord. No. 13588.The Federal Food, Drug, and Cosmetic Act and subsequent amending statutes are codified into Title 21 Chapter 9 of the United States Code. The listing of FD&C Act sections presented here identifies both the FD&C Act and U.S Federal food drug and cosmetic act 21 u.s.c 321. Code section numbers, which can be used to narrow your search on the Law Revision Counsel website.

(b) The definitions and interpretations of terms contained in sections 201 and 900 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321 and 387) shall be applicable also to such terms when used in regulations promulgated under that act.The Secretary of Health and Human Services (HHS) is issuing this notice pursuant to section 564 of the Federal Food, Drug, and Cosmetic (FD&C) Act. On February 4, 2020, the Secretary determined pursuant to his authority under section 564 of the FD&C Act that there is a public healthDisposición publicada en US Code, Title 21. FOOD AND DRUGS, Chapter 9. Federal Food, Drug, and Cosmetic Act, Subchapter II. Definitions. VLEX-670966397

21 U.S. Code § 360. Registration of producers of drugs or devices. the term “name” shall include in the case of a partnership the name of each partner and, in the case of a corporation, the name of each corporate officer and director, and the State of incorporation.

Federal food drug and cosmetic act 21 u.s.c 321 download

This part governs the practices and procedures applicable to regulatory enforcement actions initiated by the Food and Drug Administration pursuant to the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.) and other laws that it administers.Categories/Foods Minimum Requirements and Specifications WIC formula Infant formula Exempt infant formula All authorized infant formulas must (1) meet the definition for an infant formula in section 201(z) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(z)) and meet the requirements for an infant formula under section 412 of theUS Code Title 21 Chapter 9 Federal Food, Drug, and Cosmetic Act. US Code Title 21 Chapter 9 Federal Food, Drug, and Cosmetic Act. § 321 - Definitions.

Federal food drug and cosmetic act 21 u.s.c 321 best

Nothing in this Act (or the amendments made by this Act) shall be construed to apply with respect to drugs that are not also cosmetics (as such terms are defined in section 201 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321)). Speaker of the House of Representatives. Vice President of the United States and President of the Senate.Home > Regulatory Information > Legislation > Federal Food, Drug, and Cosmetic Act (FD&C Act) FD&C Act Chapter IV: Food > Sec. 409. [21 USC §348] Unsafe Food Additives 11/29/11 2:25 PM(b) The definitions and interpretations of terms contained in sections 201 and 900 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321 and 387) shall be applicable also to such terms when used in regulations promulgated under that act.