[Code of Federal Regulations]
[Title 21, Volume 1]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR1.1]

[Page 5]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                                SERVICES
 
PART 1--GENERAL ENFORCEMENT REGULATIONS--Table of Contents
 
                      Subpart A--General Provisions
 
Sec. 1.1  General.


    (a) The provisions of regulations promulgated under the Federal 
Food, Drug, and Cosmetic Act with respect to the doing of any act shall 
be applicable also to the causing of such act to be done.
    (b) The definitions and interpretations of terms contained in 
section 201 of the Federal Food, Drug, and Cosmetic Act shall be 
applicable also to such terms when used in regulations promulgated under 
that act.
    (c) The definition of package in Sec. 1.20 and of principal display 
panel in Secs. 101.1, 201.60, 501.1, 701.10 and 801.60 of this chapter; 
and the requirements pertaining to uniform location, lack of 
qualification, and separation of the net quantity declaration in 
Secs. 101.105(f), 201.62(e), 501.105(f), 701.13(f) and 801.62(e) of this 
chapter to type size requirements for net quantity declaration in 
Secs. 101.105(i), 201.62(h), 501.105(i), 701.13(i) and 801.62(h) of this 
chapter, to initial statement of ounces in the dual declaration of net 
quantity in Secs. 101.105(j) and (m), 201.62(i) and (k), 501.105(j) and 
(m), 701.13(j) and (m) and 801.62(i) and (k) of this chapter, to initial 
statement of inches in declaration of net quantity in Secs. 201.62(m), 
701.13(o) and 801.62(m) of this chapter, to initial statement of square 
inches in declaration of net quantity in Secs. 201.62(n), 701.13(p) and 
801.62(n) of this chapter, to prohibition of certain supplemental net 
quantity statements in Secs. 101.105(o), 201.62(o), 501.105(o), 
701.13(q) and 801.62(o) of this chapter, and to servings representations 
in Sec. 501.8 of this chapter are provided for solely by the Fair 
Packaging and Labeling Act. The other requirements of this part are 
issued under both the Fair Packaging and Labeling Act and the Federal 
Food, Drug, and Cosmetic Act, or by the latter act solely, and are not 
limited in their application by section 10 of the Fair Packaging and 
Labeling Act.

[42 FR 15553, Mar. 22, 1977, as amended at 58 FR 17085, Apr. 1, 1993]