of such payment, shall constitute a lien against any future importations made by such owner or consignee. (d) A food, drug, device, or cosmetic intended for export shall not be deemed to be adulterated or misbranded under this Act if it (1) accords to the specifications of the foreign purchaser, (2) is not in conflict with the laws of the country to which it is intended for export, and (3) is labeled on the outside of the shipping package to show that it is intended for export. But if such article is sold or offered for sale in domestic commerce, this subsection shall not exempt it from any of the provisions of this Act. Nothing in this subsection shall authorize the exportation of any new animal drug, or an animal feed bearing or containing a new animal drug, which is unsafe within the meaning of section 512 of this Act. CHAPTER IX-MISCELLANEOUS SEPARABILITY CLAUSE SEC. 901 [391]. If any provision of this Act is declared unconstitutional, or the applicability thereof to any person or circumstances is held invalid, the constitutionality of the remainder of the Act and the applicability thereof to other persons and circumstances shall not be affected thereby. EFFECTIVE DATE AND REPEALS SEC. 902 [392]. (a) This Act shall take effect twelve months after the date of its enactment. The Federal Food and Drug Act of June 30, 1906, as amended (U.S.C., 1934 ed., title 21, secs. 1-15), shall remain in force until such effective date, and except as otherwise provided in this subsection, is hereby repealed effective upon such date: Provided, That the provisions of section 701 shall become effective on the enactment of this Act, and thereafter the Secretary [of Agriculture] is authorized hereby to (1) conduct hearings and to promulgate regulations which shall become effective on or after the effective date of this Act as the Secretary [of Agriculture] shall direct, and (2) designate prior to the effective date of this Act food having common or usual names and exempt such food from the requirements of clause (2) of section 403 (i) for a reasonable time to permit the formulation, promulgation, and effective application of definitions and standards of identity therefor as provided by section 401: Provided further, That sections 502(j), 505, and 601(a), and all other provisions of this Act to the extent that they may relate to the enforcement of such sections, shall take effect on the date of the enactment of this Act, except that in the case of a cosmetic to which the proviso of section 601 (a) relates, such cosmetic shall not, prior to the ninetieth day after such date of enactment, be deemed adulterated by reason of the failure of its label to bear the legend prescribed in such proviso: Provided further, That the Act of March 4, 1923 (U.S.C., 1945 ed. (title 21, sec. 321a; 32 Stat. 1500, ch. 268), defining butter and providing a standard therefor; the Act of July 24, 1919 (U.S.C., 1946 ed., title 21, sec. 321b; 41 Stat. 271, ch. 26), defining wrapped meats as in package form; and the amendment to the Food and Drug Act, section 10A, approved August 27, 1935 (U.S.C., 1946 ed., title 21, sec. 372a [49 Stat. 871, ch. 739]), shall remain in force and effect and be applicable to the provisions of this Act. (b) Meats and meat food products shall be exempt from the provisions of this Act to the extent of the application or the extension thereto of the Meat Inspection Act, approved March 4, 1907, as amended (U.S.C., 1946 ed., title 21, secs. 71-96; 34 Stat. 1260 et seq.). (c) Nothing contained in this Act shall be construed as in any way affecting, modifying, repealing, or superseding the provisions of section 351 of Public Health Service Act (relating to viruses, serums, toxins, and analogous products applicable to man); the virus, serum, toxin, and analogous products provisions, applicable to domestic animals, of the Act of Congress approved March 4, 1913 (37 Stat. 832-833); the Filled Cheese Act of June 6, 1896 (U.S.C., 1946 ed., title 26, ch. 17, secs. 2350-2362); the Filled Milk Act of March 4, 1923 (U.S.C. 1946 ed., title 21, ch. 3, secs. 61-64); or the Import Milk Act of February 15, 1927 (U.S.C., 1946 ed., title 21, ch. 4, secs. 141-149). (Approved June 25, 1938.) CONTROLLED SUBSTANCES ACT [Title II of the Comprehensive Drug Abuse Prevention and Control Act of 1970] TABLE OF CONTENTS TITLE II-CONTROL AND ENFORCEMENT PART A-SHORT TITLE; FINDINGS AND DECLARATION; DEFINITIONS Sec. 100. Short title. Sec. 101. Findings and declarations. Sec. 102. Definitions. Sec. 103. Increased numbers of enforcement personnel. PART B-AUTHORITY TO CONTROL; STANDARDS AND SCHEDULES Sec. 201. Authority and criteria for classification of substances. PART C-REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, AND Sec. 301. Rules and regulations. Sec. 302. Persons required to register. Sec. 303. Registration requirements. Sec. 304. Denial, revocation, or suspension of registration. Sec. 305. Labeling and packaging requirements. Sec. 306. Quotas applicable to certain substances. Sec. 307. Records and reports of registrants. Sec. 308. Order forms. Sec. 309. Prescriptions. PART D-OFFENSES AND PENALTIES Sec. 401. Prohibited acts A-penalties. Sec. 404. Penalty for simple possession; conditional discharge Sec. 405. Distribution to persons under age twenty-one. Sec. 406. Attempt and conspiracy. Sec. 407. Additional penalties. Sec. 408. Continuing criminal enterprise. Sec. 409. Dangerous special drug offender sentencing. Sec. 410. Information for sentencing. Sec. 411. Proceedings to establish previous convictions. PART E-ADMINISTRATIVE AND ENFORCEMENT PROVISIONS Sec. 501. Procedures. Sec. 502. Education and research programs of the Attorney Gen eral. Sec. 503. Cooperative arrangements. Sec. 504. Advisory committees. Sec. 505. Administrative hearings. Sec. 507. Judicial review. |