Mo. Code Regs. tit. 2 § 70-30.040

Current through Register Vol. 49, No. 21, November 1, 2024.
Section 2 CSR 70-30.040 - Expression of Guarantees

PURPOSE: This rule establishes what must be guaranteed and how the guarantees must be expressed.

(1) The guarantees for crude protein, equivalent crude protein from nonprotein nitrogen, lysine, methionine, other amino acids, crude fat, crude fiber and acid detergent fiber will be in terms of percentage.
(2) Mineral Guarantees.
(A) When the calcium, salt, and sodium guarantees are given in the guaranteed analysis such shall be stated and conform to the following:
1. When the minimum is below two and one-half percent (2.5%), the maximum shall not exceed the minimum by more than one-half (0.5) percentage point;
2. When the minimum is two and one-half percent (2.5%) but less than five percent (5.0%), the maximum shall not exceed the minimum by more than one (1) percentage point; and
3. When the minimum is above five percent (5.0%) or greater, the maximum shall not exceed the minimum by more than twenty percent (20%) of the minimum and in no case shall the maximum exceed the minimum by more than five (5) percentage points.
(B) When stated, guarantees for minimum and maximum total sodium and salt, minimum potassium, magnesium, sulfur, phosphorus and maximum fluoride shall be in terms of percentage. Other minimum mineral guarantees shall be stated in parts per million (ppm) when the concentration is less than ten thousand (10,000) ppm and in percentage when the concentration is ten thousand (10,000) ppm one percent (1%) or greater.
(C) Products labeled with a quantity statement (e.g., tablets, capsules, granules, or liquid) may state mineral guarantees in milligrams (mg) per units (e.g., tablets, capsules, granules, or liquids) consistent with the quantity statement and directions for use.
(3) Guarantees for minimum vitamin content of commercial feeds shall be listed in the order specified and are stated in mg/lb. or in units consistent with those employed for the quantity statement unless otherwise specified-
(A) Vitamin A, other than precursors of vitamin A, International Units per pound;
(B) Vitamin D-3, in products offered for poultry feeding, in International Chick Units per pound;
(C) Vitamin D for other uses, International Units per pound;
(D) Vitamin E, in International Units per pound;
(E) Concentrated oils and feed additive premixes containing vitamins A, D, and/or E may, at the option of the distributor, be stated in units per gram instead of units per pound;
(F) Vitamin B-12, in milligrams or micro-grams per pound; and
(G) All other vitamin guarantees shall express the vitamin activity in milligrams per pound in terms of the following: menadione, riboflavin, d-pantothenic acid, thiamine, niacin, vitamin B-6, folic acid, choline, biotin, inositol, p-amino benzoic acid, ascorbic acid, and carotene.
(4) Guarantees for drugs shall be stated in terms of percent by weight except-
(A) Antibiotics present at less than two thousand (2000) grams per ton (total) of commercial feed shall be stated in grams per ton of commercial feed;
(B) Antibiotics present at two thousand (2000) or more grams per ton (total) of commercial feed shall be stated in grams per pound of commercial feed;
(C) Labels for commercial feeds containing growth promotion and/or feed efficiency levels of antibiotics, which are to be fed continuously as the sole ration, are not required to make quantitative guarantees except as specifically noted in the federal food additive regulations, for certain antibiotics, wherein, quantitative guarantees are required regardless of the level or purpose of the antibiotic; and
(D) The term milligrams per pound may be used for drugs or antibiotics in those cases where a dosage is given in "milligrams" in the feeding directions.
(5) Commercial feeds containing any added nonprotein nitrogen shall be labeled as follows:
(A) For ruminants-
1. Complete feeds, supplements and concentrates containing added nonprotein nitrogen and containing more than five percent (5%) protein from natural sources shall be guaranteed as follows: crude protein, minimum, ____% (This includes not more than ____% equivalent crude protein from non-protein nitrogen);
2. Mixed feed concentrates and supplements containing less than five percent (5%) protein from natural sources may be guaranteed as follows: equivalent crude protein from nonprotein nitrogen, minimum ____%; and
3. Ingredient sources of nonprotein nitrogen such as urea, diammonium phosphate, ammonium polyphosphate solution, ammoniated rice hulls, or other basic non-protein nitrogen ingredients defined by the Association of American Feed Control Officials, shall be guaranteed as follows: nitrogen, minimum ____%; equivalent crude protein from nonprotein nitrogen, minimum, ____%; and
(B) For nonruminants-
1. Complete feeds, supplements and concentrates containing crude protein from all forms of nonprotein nitrogen, added as such, shall be labeled as follows: crude protein, minimum, ____% (This includes not more than ____% equivalent crude protein which is not nutritionally available to (species of animal for which feed is intended)); and
2. Premixes, concentrates or supplements intended for nonruminants containing more than one and one-fourth percent (1.25%) equivalent crude protein from all forms of nonprotein nitrogen, added as such, must contain adequate directions for use and a prominent statement: WARNING: This feed must be used only in accordance with directions furnished on the label.
(6) Mineral phosphatic materials for feeding purposes shall be labeled with the guarantee for minimum and maximum percentage of calcium (when present), the minimum percentage of phosphorus and the maximum percentage of fluorine.
(7) Guarantees for microorganisms shall be stated in colony forming units per gram (CFU/g) when directions are for using the product in grams or in colony forming units per pound (CFU/lb) when directions are for using the product in pounds. A parenthetical statement following the guarantee shall list each species in order of predominance.
(8) Guarantees for enzymes shall be stated in units of enzymatic activity per unit weight or volume, consistent with label directions. The source organism for each type of enzymatic activity shall be specified, such as: Protease (Bacillus subtilis) 5.5 mg amino acids liberated/min. milligram. If two (2) or more sources have the same type of activity, they shall be listed in order of predominance based on the amount of enzymatic activity provided.

2 CSR 70-30.040

AUTHORITY: section 266.195, RSMo Supp. 1997.* Original rule filed Jan. 16, 1975, effective Feb. 1, 1975. Amended: Filed Sept. 15, 1976, effective Dec. 11, 1976. Amended: Filed May 13, 1986, effective Sept. 1, 1986. Amended: Filed Nov. 17, 1997, effective June 30, 1998.

*Original authority 1972, amended 1993, 1995, 1997.