Kansas Administrative Code

General conformity of feder- al actions. (a) 40 CFR part 93, subpart B, as pro- mulgated on November 30, 1993, is adopted by reference, except for 40 CFR 93.151 and 40 CFR 93.160(f) which are deleted. (b) Unless the context clearly indicates other- wise: (1) the term “state” shal…

Transportation conformity. (a) The provisions of this regulation shall apply: (1) to areas of the state which have been iden- tified as not meeting the national primary ambi- ent air quality standard for ozone in the manner prescribed by the provisions of section 107(d) of the fe…

Environmental impact mon- itoring. (a) On or before April 1 of each year, the department of health and environment shall notify the owner or operator of each power gen- eration facility of any environmental impact mon- itoring activities that the Department proposes to conduct at…

Fee determination basis. (a) The fee to be collected for determining and monitoring the environmental impact of a power generation facility during any 12 month period in- cluded under the provisions of K.A.R. 28-19-81(a) shall be determined upon the basis of the type of fuel used…

(Authorized by and implementing K.S.A. 65-3005, 65-3010; effective May 1, 1986; revoked May 10, 1996.)

(Authorized by and implementing K.S.A. 65-3005, 65-3010; effective May 1, 1986; amended May 1, 1988; revoked May 10, 1996.) NEW SOURCE PERFORMANCE STANDARDS

(Authorized by and implementing K.S.A. 65-3005, 65-3010; effective May 1, 1983; amended May 1, 1986; amended May 1, 1988; re- voked May 10, 1996.)

(Authorized by and implementing K.S.A. 65-3005, 65-3010; effective May 1, 1983; amended May 1, 1986; amended May 1, 1987; amended May 1, 1988; revoked May 10, 1996.) 28-19-87 to 28-19-95. (Authorized by andimplementingK.S.A.65-3005,65-3010;effec- 419 Ambient Air Quality Standards…

Time schedule for compliance. Except as otherwise noted in specific emission control regulations, compliance with these regula- tionsshallbeaccordingtothefollowingschedules: (a) All new air contaminant emission sources or alterations to emission sources that are required to be re…

(Authorized by and implement- ing K.S.A. 65-3005, 65-3010; effective May 1, 1983; amended May 1, 1986; amended May 1, 1987; amended May 1, 1988; revoked May 10, 1996.)

(Authorized by and implementing K.S.A. 65-3005, 65-3010; effective May 1, 1983; revoked May 1, 1986.)

(Authorized by and implementing K.S.A. 65-3005, 65-3010; effective May 1, 1983; amended May 1, 1986; amended May 1, 1987; amended May 1, 1988; revoked May 10, 1996.)

(Authorized by and implement- ing K.S.A. 65-3005, 65-3010; effective May 1, 1986; amended May 1, 1987; amended May 1, 1988; revoked May 10, 1996.) 28-19-99 to 28-19-103. (Authorized by andimplementingK.S.A.65-3005,65-3010;effec- tive May 1, 1983; amended May 1, 1986; amended May …

(Authorized by K.S.A. 65-102, 65- 1638, 65-1639; effective Jan. 1, 1966; amended Jan. 1, 1969; revoked May 1, 1981.)

(Authorized by K.S.A. 65-102, K.S.A. 1968 Supp. 65-128; effective Jan. 1, 1966; revoked Jan. 1, 1969.)

(Authorized by K.S.A. 65-102, 65- 128; effective Jan. 1, 1969; revoked May 1, 1981.)

(Authorized by K.S.A. 65-102; ef- fective Jan. 1, 1966; revoked Jan. 1, 1969.)

(Authorized by K.S.A. 65-101, 65-102, 65-128, 65-2426; effective Jan. 1, 1969; amended Jan. 1, 1972; amended May 1, 1976; re- voked May 1, 1981.)

(Authorized by K.S.A. 65-101, 65- 102, 65-128; effective Jan. 1, 1966; amended Jan. 1, 1969;amendedMay1,1976;revokedMay1,1981.)

(Authorized by K.S.A. 65-102, 65- 128; effective Jan. 1, 1966; amended Jan. 1, 1969; revoked May 1, 1981.)

(Authorized by K.S.A. 65-102; ef- fective Jan. 1, 1966; revoked May 1, 1981.)

(Authorized by K.S.A. 65-102, 65- 128; effective Jan. 1, 1966; amended Jan. 1, 1969; revoked May 1, 1981.)

(Authorized by K.S.A. 65-102; ef- fective Jan. 1, 1966; revoked May 1, 1981.) AND COSMETICS A. GENERAL REGULATIONS

(Authorized by K.S.A. 1965 Supp. 65-673; effective Jan. 1, 1966; revoked June 4, 2010.)

(Authorized by K.S.A. 65-665 (j), K.S.A. 1965 Supp. 65-673; effective Jan. 1, 1966; revoked June 4, 2010.)

(Authorized by K.S.A. 1968 Supp. 65-673; effective Jan. 1, 1969; revoked May 10, 1996.) 28-21-109 to 28-21-111. (Authorized by K.S.A. 1968 Supp. 65-673; effective Jan. 1, 1969; revoked May 10, 1996.)

(Authorized by K.S.A. 65-665 (k), K.S.A. 1965 Supp. 65-673; effective Jan. 1, 1966; revoked June 4, 2010.) B. WHEAT FLOUR AND RELATED PRODUCTS

(Authorized by K.S.A. 1968 Supp. 65-673; effective Jan. 1, 1969; revoked May 10, 1996.) I. DRUGS AND THERAPEUTIC DEVICES

(Authorized by K.S.A. 1965 Supp. 65-673; effective Jan. 1, 1966; revoked Feb. 8, 2013.)

(Authorized by K.S.A. 1979 Supp. 65-663, 65-673; effective Jan. 1, 1966; revoked May 1, 1980.)

Drugs; name. (a) The name by which a drug is designated shall be clearly dis- tinguishing and differentiating from any name recognized in an official compendium unless such drug complies in identity with the identity prescribed in an official compendium under such recognized name…

Drugs and devices; labeling, misbranding. (a) Among representations in the labeling of a drug or device which render such drug or device misbranded is a false or misleading representation with respect to another drug or de- vice or a food or cosmetic. (b) The labeling of a drug w…

Drugs and devices; labeling requirements. (a) If a drug or device is not man- ufactured by the person whose name appears on the label, the name shall be qualified by a phrase which reveals the connection such person has with such drug or device, such as “Manufactured for and Pack…

Drugs and devices; forms of making required statements. (a) A word, state- ment, or other information required by or under authority of the Act to appear on the label may lack that prominence and conspicuousness re- quired by K.S.A. 65-669(c) by reason (among oth- er reasons) of:…

Habit-forming drugs; label requirements. (a)(1) The name of a substance 499 Food, Drugs and Cosmetics 28-21-205 or derivative required to be borne on the label of a drug by K.S.A. 65-669(d) shall be the common or usual name of such substance or derivative, unless it is designated…

Drugs; statement of ingre- dients and proportion. (a)(1) The name of an ingredient, substance, derivative, or preparation required by K.S.A. 65-669(e)(1)(ii) to be borne on the label of a drug shall be the name thereof, which is listed in K.S.A. 65-669(e)(1)(ii), or, if not so li…

Drugs and devices; direc- tions for use. (a) Adequate directions for use. “Adequate directions for use” means directions under which the layman can use a drug or device safely and for the purposes for which it is intend- ed. Directions for use may be inadequate because (among oth…

(Authorized by K.S.A. 1979 Supp. 65-663; effective May 1, 1980; revoked June 4, 2010.)

(Authorized by K.S.A. 1979 Supp. 65-663, 65-673; effective Jan. 1, 1966; revoked May 1, 1980.) 493 Food, Drugs and Cosmetics 28-21-40

(Authorized by K.S.A. 1979 Supp. 65-663; effective May 1, 1980; revoked June 4, 2010.)

(Authorized by K.S.A. 1979 Supp. 65-663, 65-673; effective Jan. 1, 1966; revoked May 1, 1980.)

(Authorized by K.S.A. 1979 Supp. 65-663; effective May 1, 1980; revoked June 4, 2010.)

(Authorized by K.S.A. 1979 Supp. 65-663, 65-673; effective Jan. 1, 1966; revoked May 1, 1980.)

(Authorized by K.S.A. 1979 Supp. 65-663; effective May 1, 1980; revoked June 4, 2010.)

(Authorized by K.S.A. 1979 Supp. 65-663, 65-673; effective Jan. 1, 1966; revoked May 1, 1980.)

(Authorized by K.S.A. 1979 Supp. 65-663; effective May 1, 1980; revoked June 4, 2010.)

(Authorized by K.S.A. 1979 Supp. 65-663, 65-673; effective Jan. 1, 1966; revoked May 1, 1980.)

Definitions. (a) The term “laetrile” (with a small l) is a generic term which is used interchangeably with “Laetrile,” “nitrilo- side,” “amygdalin,” “vitamin B-17” and related compounds of unknown number. The term is also used to include a number of these compounds, in which case…

Manufacturing practice. (a) The criteria in each section of this regulation shall applyindeterminingwhetherthemethodsusedin, or the facilities or controls used for, the manufac- ture, processing, packing, or holding of the product conform to or are operated or administered in con…

Personnel. (a) The personnel responsible for directing the manufacture and control of amygdalin (laetrile) shall be adequate in number and background of education, training and experience, or combination thereof, to assure that the product has the safety, identity, strength, qual…