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15 U.S.C. § 55 — Additional definitions
Federal law — U.S. Code and appendices · legal_authorities
Page 76
TITLE 15—COMMERCE AND TRADE
§ 55
rious to health at the time the same leave offi-
cial ‘‘establishments.’’
(b) Exception of advertising medium or agency
No publisher, radio-broadcast licensee, or
agency or medium for the dissemination of ad-
vertising, except the manufacturer, packer, dis-
tributor, or seller of the commodity to which
the false advertisement relates, shall be liable
under this section by reason of the dissemina-
tion by him of any false advertisement, unless
he has refused, on the request of the Commis-
sion, to furnish the Commission the name and
post-office address of the manufacturer, packer,
distributor, seller, or advertising agency, resid-
ing in the United States, who caused him to dis-
seminate such advertisement. No advertising
agency shall be liable under this section by rea-
son of the causing by it of the dissemination of
any false advertisement, unless it has refused,
on the request of the Commission, to furnish the
Commission the name and post-office address of
the manufacturer, packer, distributor, or seller,
residing in the United States, who caused it to
cause the dissemination of such advertisement.
(Sept. 26, 1914, ch. 311, § 14, as added Mar. 21, 1938,
ch. 49, § 4, 52 Stat. 114.)
Editorial Notes
REFERENCES IN TEXT
The Meat Inspection Act, referred to in subsec. (a), is
act Mar. 4, 1907, ch. 2907, titles I to IV, as added Dec.
15, 1967, Pub. L. 90–201, 81 Stat. 584, which is classified
to subchapters I to IV (§ 601 et seq.) of chapter 12 of
Title 21, Food and Drugs. For complete classification of
this Act to the Code, see Short Title note set out under
section 601 of Title 21 and Tables.
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE
Act Mar. 21, 1938, ch. 49, § 5(b), 52 Stat. 117, provided:
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Page 76
TITLE 15—COMMERCE AND TRADE
§ 55
rious to health at the time the same leave offi-
cial ‘‘establishments.’’
(b) Exception of advertising medium or agency
No publisher, radio-broadcast licensee, or
agency or medium for the dissemination of ad-
vertising, except the manufacturer, packer, dis-
tributor, or seller of the commodity to which
the false advertisement relates, shall be liable
under this section by reason of the dissemina-
tion by him of any false advertisement, unless
he has refused, on the request of the Commis-
sion, to furnish the Commission the name and
post-office address of the manufacturer, packer,
distributor, seller, or advertising agency, resid-
ing in the United States, who caused him to dis-
seminate such advertisement. No advertising
agency shall be liable under this section by rea-
son of the causing by it of the dissemination of
any false advertisement, unless it has refused,
on the request of the Commission, to furnish the
Commission the name and post-office address of
the manufacturer, packer, distributor, or seller,
residing in the United States, who caused it to
cause the dissemination of such advertisement.
(Sept. 26, 1914, ch. 311, § 14, as added Mar. 21, 1938,
ch. 49, § 4, 52 Stat. 114.)
Editorial Notes
REFERENCES IN TEXT
The Meat Inspection Act, referred to in subsec. (a), is
act Mar. 4, 1907, ch. 2907, titles I to IV, as added Dec.
15, 1967, Pub. L. 90–201, 81 Stat. 584, which is classified
to subchapters I to IV (§ 601 et seq.) of chapter 12 of
Title 21, Food and Drugs. For complete classification of
this Act to the Code, see Short Title note set out under
section 601 of Title 21 and Tables.
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE
Act Mar. 21, 1938, ch. 49, § 5(b), 52 Stat. 117, provided:
‘‘Section 14 of the Federal Trade Commission Act [this
section] added to such Act by section 4 of this Act,
shall take effect on the expiration of sixty days after
the date of the enactment of this Act [Mar. 21, 1938].’’
Executive Documents
TRANSFER OF FUNCTIONS
For transfer of functions of Federal Trade Commis-
sion, with certain exceptions, to Chairman of such
Commission, see Reorg. Plan No. 8 of 1950, § 1, eff. May
24, 1950, 15 F.R. 3175, 64 Stat. 1264, set out under section
41 of this title.
§ 55. Additional definitions
For the purposes of sections 52 to 54 of this
title—
(a) False advertisement
(1) The term ‘‘false advertisement’’ means an
advertisement, other than labeling, which is
misleading in a material respect; and in deter-
mining whether any advertisement is mis-
leading, there shall be taken into account
(among other things) not only representations
made or suggested by statement, word, design,
device, sound, or any combination thereof, but
also the extent to which the advertisement fails
to reveal facts material in the light of such rep-
resentations or material with respect to con-
sequences which may result from the use of the
commodity to which the advertisement relates
under the conditions prescribed in said adver-
tisement, or under such conditions as are cus-
tomary or usual. No advertisement of a drug
shall be deemed to be false if it is disseminated
only to members of the medical profession, con-
tains no false representation of a material fact,
and includes, or is accompanied in each instance
by truthful disclosure of, the formula showing
quantitatively each ingredient of such drug.
(2) In the case of oleomargarine or margarine
an advertisement shall be deemed misleading in
a material respect if in such advertisement rep-
resentations are made or suggested by state-
ment, word, grade designation, design, device,
symbol, sound, or any combination thereof, that
such oleomargarine or margarine is a dairy
product, except that nothing contained herein
shall prevent a truthful, accurate, and full
statement in any such advertisement of all the
ingredients contained in such oleomargarine or
margarine.
(b) Food
The term ‘‘food’’ means (1) articles used for
food or drink for man or other animals, (2) chew-
ing gum, and (3) articles used for components of
any such article.
(c) Drug
The term ‘‘drug’’ means (1) articles recognized
in the official United States Pharmacopoeia, of-
ficial
Homoeopathic
Pharmacopoeia
of
the
United States, or official National Formulary,
or any supplement to any of them; and (2) arti-
cles intended for use in the diagnosis, cure, miti-
gation, treatment, or prevention of disease in
man or other animals; and (3) articles (other
than food) intended to affect the structure or
any function of the body of man or other ani-
mals; and (4) articles intended for use as a com-
ponent of any article specified in clause (1), (2),
or (3); but does not include devices or their com-
ponents, parts, or accessories.
(d) Device
The term ‘‘device’’ (except when used in sub-
section (a) of this section) means an instrument,
apparatus, implement, machine, contrivance,
implant, in vitro reagent, or other similar or re-
lated article, including any component, part, or
accessory, which is—
(1) recognized in the official National For-
mulary, or the United States Pharmacopeia,
or any supplement to them,
(2) intended for use in the diagnosis of dis-
ease or other conditions, or in the cure, miti-
gation, treatment, or prevention of disease, in
man or other animals, or
(3) intended to affect the structure or any
function of the body of man or other animals,
and
which does not achieve any of its principal in-
tended purposes through chemical action within
or on the body of man or other animals and
which is not dependent upon being metabolized
for the achievement of any of its principal in-
tended purposes.
(e) Cosmetic
The term ‘‘cosmetic’’ means (1) articles to be
rubbed, poured, sprinkled, or sprayed on, intro-
Page 77
TITLE 15—COMMERCE AND TRADE
§ 56
duced into, or otherwise applied to the human
body or any part thereof intended for cleansing,
beautifying, promoting attractiveness, or alter-
ing the appearance, and (2) articles intended for
use as a component of any such article; except
that such term shall not include soap.
(f) Oleomargarine or margarine
For the purposes of this section and section
347 of title 21, the term ‘‘oleomargarine’’ or
‘‘margarine’’ includes—
(1) all substances, mixtures, and compounds
known as oleomargarine or margarine;
(2) all substances, mixtures, and compounds
which have a consistence similar to that of
butter and which contain any edible oils or
fats other than milk fat if made in imitation
or semblance of butter.
(Sept. 26, 1914, ch. 311, § 15, as added Mar. 21, 1938,
ch. 49, § 4, 52 Stat. 114; amended Mar. 16, 1950, ch.
61, § 4(a), (b), 64 Stat. 21; Pub. L. 94–295,
§ 3(a)(1)(B), May 28, 1976, 90 Stat. 575.)
Editorial Notes
AMENDMENTS
1976—Subsec. (d). Pub. L. 94–295 expanded definition
of ‘‘device’’ to include implements, machines, implants,
in vitro reagents, and other similar or related articles,
added recognition in the National Formulary or the
United States Pharmacopeia, or any supplement to the
Formulary or Pharmacopeia, to the enumeration of
conditions under which a device may qualify for inclu-
sion under this chapter, and inserted requirements that
a device be one which does not achieve any of its prin-
cipal intended purposes through chemical action within
or on the body of man or other animals and which is
not dependent upon being metabolized for the achieve-
ment of any of its principal intended purposes.
1950—Subsec. (a). Act Mar. 16, 1950, § 4(a), designated
existing provisions as par. (1) and added par. (2) relat-
ing to oleomargarine.
Subsec. (f). Act Mar. 16, 1950, § 4(b), added subsec. (f).
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE OF 1950 AMENDMENT
Amendment by act Mar. 16, 1950, effective July 1, 1950,
see note set out under section 347 of Title 21, Food and
Drugs.
§ 56. Commencement, defense, intervention and
supervision of litigation and appeal by Com-
mission or Attorney General
(a) Procedure for exercise of authority to litigate
or appeal
(1) Except as otherwise provided in paragraph
(2) or (3), if—
(A) before commencing, defending, or inter-
vening in, any civil action involving this sub-
chapter (including an action to collect a civil
penalty) which the Commission, or the Attor-
ney General on behalf of the Commission, is
authorized to commence, defend, or intervene
in, the Commission gives written notification
and undertakes to consult with the Attorney
General with respect to such action; and
(B) the Attorney General fails within 45 days
after receipt of such notification to com-
mence, defend, or intervene in, such action;
the Commission may commence, defend, or in-
tervene in, and supervise the litigation of, such
action and any appeal of such action in its own
name by any of its attorneys designated by it
for such purpose.
(2) Except as otherwise provided in paragraph
(3), in any civil action—
(A) under section 53 of this title (relating to
injunctive relief);
(B) under section 57b of this title (relating to
consumer redress);
(C) to obtain judicial review of a rule pre-
scribed by the Commission, or a cease and de-
sist order issued under section 45 of this title;
(D) under the second paragraph of section 49
of this title (relating to enforcement of a sub-
pena) and under the fourth paragraph of such
section (relating to compliance with section 46
of this title); or
(E) under section 57b–2a of this title;
the Commission shall have exclusive authority
to commence or defend, and supervise the litiga-
tion of, such action and any appeal of such ac-
tion in its own name by any of its attorneys des-
ignated by it for such purpose, unless the Com-
mission authorizes the Attorney General to do
so. The Commission shall inform the Attorney
General of the exercise of such authority and
such exercise shall not preclude the Attorney
General from intervening on behalf of the
United States in such action and any appeal of
such action as may be otherwise provided by
law.
(3)(A) If the Commission makes a written re-
quest to the Attorney General, within the 10-day
period which begins on the date of the entry of
the judgment in any civil action in which the
Commission represented itself pursuant to para-
graph (1) or (2), to represent itself through any
of its attorneys designated by it for such pur-
pose before the Supreme Court in such action, it
may do so, if—
(i) the Attorney General concurs with such
request; or
(ii) the Attorney General, within the 60-day
period which begins on the date of the entry of
such judgment—
(a) refuses to appeal or file a petition for
writ of certiorari with respect to such civil
action, in which case he shall give written
notification to the Commission of the rea-
sons for such refusal within such 60-day pe-
riod; or
(b) the Attorney General fails to take any
action with respect to the Commission’s re-
quest.
(B) In any case where the Attorney General
represents the Commission before the Supreme
Court in any civil action in which the Commis-
sion represented itself pursuant to paragraph (1)
or (2), the Attorney General may not agree to
any settlement, compromise, or dismissal of
such action, or confess error in the Supreme
Court with respect to such action, unless the
Commission concurs.
(C) For purposes of this paragraph (with re-
spect to representation before the Supreme
Court), the term ‘‘Attorney General’’ includes
the Solicitor General.
(4) If, prior to the expiration of the 45-day pe-
riod specified in paragraph (1) of this section or
a 60-day period specified in paragraph (3), any
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Federal law — U.S. Code and appendices · legal_authorities
For the purposes of sections 52 to 54 of this title—
**(a) False advertisement**
(1) The term “false advertisement” means an advertisement, other than labeling, which is misleading in a material respect; and in determining whether any advertisement is misleading, there shall be taken into account (among other things) not only representations made or suggested by statement, word, design, device, sound, or any combination thereof, but also the extent to which the advertisement fails to reveal facts material in the light of such representations or material with respect to consequences which may result from the use of the commodity to which the advertisement relates under the conditions prescribed in said advertisement, or under such conditions as are customary or usual. No advertisement of a drug shall be deemed to be false if it is disseminated only to members of the medical profession, contains no false representation of a material fact, and includes, or is accompanied in each instance by truthful disclosure of, the formula showing quantitatively each ingredient of such drug.
(2) In the case of oleomargarine or margarine an advertisement shall be deemed misleading in a material respect if in such advertisement representations are made or suggested by statement, word, grade designation, design, device, symbol, sound, or any combination thereof, that such oleomargarine or margarine is a dairy product, except that nothing contained herein shall prevent a truthful, accurate, and full statement in any such advertisement of all the ingredients contained in such oleomargarine or margarine.
**(b) Food** The term “food” means (1) articles used for food or drink for man or other animals, (2) chewing gum, and (3) articles used for components of any such article.
**(c) Drug** T
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 55
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