(C) The required directions for use and precautionary statements or reference to  
					their location if the detailed feeding directions and precautionary statements  
					required by R 285.635.11 and R 285.635.12 appear elsewhere on the label.  
					(D) An active drug ingredient statement listing the active drug ingredients by  
					their established name and the amounts pursuant to R 285.635.8(4).  
					(iv) The guaranteed analysis of the feed as required under section 5(1)(d) of  
					the act, including the following items, unless exempted, and in the order listed:  
					(A) Minimum percentage of crude protein.  
					(B) Maximum or minimum percentage of equivalent protein from nonprotein nitrogen  
					as required in R 285.635.8(5).  
					(C) Minimum percentage of crude fat.  
					(D) Maximum percentage of crude fiber.  
					(E) Minerals, to include in the following order:  
					Minimum  
					and  
					maximum  
					percentages of calcium (Ca), minimum percentages of phosphorus (P), minimum  
					and maximum percentages of salt (NaCl), and other minerals.  
					(F) Vitamins in such terms as specified in R 285.635.8(3).  
					(G) Total sugars as invert in dried molasses products or in products being sold  
					primarily for their molasses content.  
					(H) Exemptions to the above guaranteed analysis requirements consist  
					following:  
					of the  
					1. Guarantees for minerals are not required when specific label claims do not exist and  
					when the commercial feed contains less than 6 1/2% of total mineral elements.  
					2. Guarantees for vitamins are not required when the commercial feed is neither  
					formulated for, nor represented in any manner as, a vitamin supplement.  
					3. Guarantees for crude protein, crude fat, and crude fiber are not required when  
					the commercial feed is intended for purposes other than to furnish these substances or  
					they are of minor significance relating to the primary purpose of the product, such as  
					drug premixes, mineral or vitamin supplements, and molasses.  
					(b) The name of each ingredient as defined in the official definitions of feed  
					ingredients published in the official publication of AAFCO, common or usual name, or  
					one approved by the director, shall be used in the ingredient statement.  
					Collective terms for the  
					grouping of feed ingredients as defined in the official  
					definitions of feed ingredients published in the official publication of AAFCO, in lieu  
					of the individual ingredients, may be used if:  
					(i) Individual ingredients included in a collective term are not otherwise listed on  
					the label.  
					(ii) The manufacturer provides the director, upon request, with a listing of  
					individual ingredients within a defined group that are, or have been, used at  
					manufacturing facilities distributing in or into the state.  
					(c) The name and principal mailing address of the manufacturer or person responsible  
					for distributing the feed shall appear on the label. The principal mailing address  
					shall include the street address, city, state and zip code; however, the street address  
					may be omitted if it is shown in the current city directory or telephone directory.  
					(d) The information required in section 5(1)(a) to (e) of the act shall appear in its  
					entirety on one side of the label or on one side of the container. The information  
					required by section 5(1)(f) and (g) of the act shall be displayed in a prominent place on  
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