Iowa Admin. Code r. 21-41.2 - Label format
Cornmercial feed, other than customer-formula feed, shall be
labeled with the information prescribed in this rule on the principal display
panel of
1. Product name and brand name, if any, as
stipulated in 41.3(1).
2. If a drug
is used, label as stipulated in 41.3(2).
3. Purpose statement as stipulated in
41.3(3).
4. Guaranteed analysis as
stipulated in 41.3(4).
5. Feed
ingredients as stipulated in 41.3(5).
6. Directions for use and precautionary
statements as stipulated in 41.3(6).
7. Name and principal mailing address of the
manufacturer or person responsible for distributing the feed as stipulated in
41.3(7).
8. Quantity statement.
(1) The information required in 41.2"1" to
41.2"5," 41.2"7" and 41.2"8" must appear in its entirety on one side of the
label or on one side of the container The information required by 41.2"6" shall
be displayed in a prominent place on the label or container but not necessarily
on the same side as the above information. When the information required by
41.2"6" is placed on a different side of the label or container, it must be
referenced on the front side with a statement such as "See back of label for
directions for use." None of the information required by 41.2(198) shall be
subordinated or obscured by other statements or designs.
(2) Customer-formula feed shall be
acCornpanied with the information prescribed in this regulation using labels,
invoice, delivery ticket, or other shipping document bearing the following
information.
a. The name and address of the
manufacturer
b. The name and
address of the purchaser
c. The
date of sale or delivery.
d. The
customer-formula feed name and brand name if any.
e. The product name and net quantity of each
registered Cornmercial feed and each other ingredient used in the
mixture.
f. The directions for use
and precautionary statements as required by 41.7(198) and 41.8(198).
g. If a drug-containing product is used:
(1) The purpose of the medication (claim
statement).
(2) The established
name of each active drug ingredient and the level of each drug used in the
final mixture expressed in accordance with 41.4(4).
Notes
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