Fla. Admin. Code Ann. R. 5E-3.008 - Medicated Feed
(1) Before distribution
in Florida, a feed containing an active drug ingredient shall be labeled to
show the information required by Chapter 580, F.S., and all labeling required
by the Federal Food and Drug Administration.
(2) Customer-formula medicated feeds shall
have the labeling required under subsection (1) on each label for the lot
except that the statement of purpose of the medication and the feeding
directions may be attached to the delivery ticket supplied to the purchaser
with the delivery.
(3) Mixed feed
described under Section
580.031(2)(c),
F.S., shall bear the labeling required for customer-formula medicated feed if
an active drug ingredient is present.
(4) The regulations prescribing good
manufacturing practices for medicated feeds as published in the Code of Federal
Regulations, Title 21, Part 225, and for medicated premixes as published in
Title 21, Part 226, as of 4/1/01, are adopted as good manufacturing practices
under Chapter 580, F.S.
Notes
Rulemaking Authority 570.07(23), 580.036(2) FS. Law Implemented 580.051(1)(c), 580.071(1), (3), 580.081, 580.112 FS.
New 12-30-70, 4-3-85, Formerly 5E-3.08, Amended 6-1-95, 11-14-01.
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