New Mexico Administrative Code
Title 21 - AGRICULTURE AND RANCHING
Chapter 18 - SEEDS, FEEDS, AND FERTILIZERS
Part 3 - COMMERCIAL FEEDS
Section 21.18.3.15 - DRUG AND FEED ADDITIVES
Universal Citation: 21 NM Admin Code 21.18.3.15
Current through Register Vol. 35, No. 18, September 24, 2024
A. Prior to approval of a registration application or approval of a label for commercial feed which contain additives (including drugs, other special purpose additives, or non-nutritive additives) the distributor may be required to submit evidence to prove the safety and efficacy of the commercial feed when used according to the directions furnished on the label.
B. Satisfactory evidence of safety and efficacy of a commercial feed may be:
(1)
when the commercial feed contains such additives, the use of which conforms to
the requirements of the applicable regulation in the "Code of Federal
Regulations, Title 21", or which are "prior sanctioned" or "informal review
sanctioned" or "generally recognized as safe" for such use; or
(2) when the commercial feed is itself a drug
as defined in
76-19A-2
I, NMSA 1978 and is generally recognized as safe and effective for the labeled
use or is marketed subject to an application approved by the food and drug
administration under Title
21 U.S.C.
360 b; or
(3) when one of the purposes for feeding a
commercial feed is to impart immunity (that is to act through some
immunological process) the constituents imparting immunity have been approved
for the purpose through the Federal Virus, Serum and Toxins Act of 1913, as
amended; or
(4) when the commercial
feed is a direct fed microbial product and:
(a) the product meets the particular
fermentation product definition; and
(b) the microbial content statement, as
expressed in the labeling, is limited to the following: "contains a source of
live (viable) naturally occurring microorganisms;" this statement shall appear
on the label; and
(c) the source is
stated with a corresponding guarantee expressed in accordance with Subsection G
of 21.18.3.10 NMAC;
(5)
when the commercial feed is an enzyme product and:
(a) the product meets the particular enzyme
definition defined by the association of American feed control officials;
and
(b) the enzyme is stated with a
corresponding guarantee expressed in accordance with Subsection H of 21.18.3.10
NMAC.
Disclaimer: These regulations may not be the most recent version. New Mexico may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
This site is protected by reCAPTCHA and the Google
Privacy Policy and
Terms of Service apply.
