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505 ILCS 30/7
(505 ILCS 30/7) (from Ch. 56 1/2, par. 66.7)
Sec. 7.
Adulteration.
A commercial feed is adulterated:
(a) If it bears or contains any poisonous or deleterious substance
which may render it injurious to health; but in case the substance is not
an added substance, the commercial feed shall not be considered
adulterated if the quantity of the substance in such commercial feed does
not ordinarily render it injurious to health.
(b) If it bears or contains any poisonous, deleterious or non-nutritive
ingredient that has been added in sufficient amount to render it unsafe
within the meaning of Section 406 of the Federal Food, Drug and Cosmetic
Act, other than one which is a pesticide chemical in or on a raw
agricultural commodity or a food additive.
(c) If it is, bears or contains any food additive which is unsafe
within the meaning of Section 409 of the Federal Food, Drug and Cosmetic Act.
(d) If it is a raw agricultural commodity and it bears or contains a
pesticide chemical which is unsafe within the meaning of Section 408 of the
Federal Food, Drug and Cosmetic Act, provided, that where a pesticide
chemical has been used in or on a raw agricultural commodity in conformity
with an exemption granted or a tolerance prescribed under Section 408 of
the Federal Food, Drug and Cosmetic Act and the raw agricultural commodity
has been subjected to processing, such as, canning, cooking, freezing,
dehydrating or milling, the residue of the pesticide chemical remaining in
or on
the processed feed shall not be deemed unsafe if such residue in or on
the raw agricultural commodity has been removed to the extent possible
by good manufacturing practices as adopted and the concentration of the
residue in the processed feed is not greater than the tolerance prescribed
for the raw agricultural commodity, unless the feeding of the processed
feed will result or is likely to result in a pesticide residue in the
edible product of the animal, which is unsafe within the meaning of Section
408 of the Federal Food, Drug and Cosmetic Act.
(e) If it is, bears or contains any color additive which is unsafe
within the meaning of Section 706 of the Federal Food, Drug and Cosmetic Act.
(f) If it contains a drug and the methods used in, or the facilities or
controls used for, its manufacture, processing, or packaging do not conform
to current good manufacturing practice regulations promulgated by the
Director to assure that the drug meets the requirements of this Act as to
safety and has the identity and strength and meets the quality and purity
characteristics which it purports or is represented to possess. In
promulgating these regulations, the Director shall adopt the current good
manufacturing practice regulations for Type A medicated articles and Type B
and Type C medicated feeds established under authority of the Federal Food,
Drug, and Cosmetic Act, unless he determines that they are not appropriate
to the conditions which exist in this State.
(g) If any valuable constituent has been in whole or in part omitted or
abstracted therefrom or any less valuable substance substituted therefor.
(h) If its composition or quality falls below or differs from that which
it is purported or is represented to possess by its labeling.
(i) If it contains weed seeds in amounts exceeding the
limits established by regulation.
(Source: P.A. 87-664.)
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