SECOND REGULAR SESSION

HOUSE BILL NO. 1642

94TH GENERAL ASSEMBLY


 

 

INTRODUCED BY REPRESENTATIVE LIPKE.

                  Read 1st time January 15, 2008 and copies ordered printed.

D. ADAM CRUMBLISS, Chief Clerk

3718L.01I


 

AN ACT

To repeal sections 50.565, 192.925, 195.017, 195.217, 210.1012, 217.670, 217.690, 302.060, 304.230, 311.310, 311.325, 311.326, 409.5-508, 409.6-604, 479.260, 488.5025, 491.170, 545.050, 550.040, 559.021, 559.106, 561.031, 565.063, 565.081, 570.040, 573.037, 575.080, 575.150, 577.023, 577.500, 577.505, 578.250, 578.255, 578.260, 578.265, 590.190, 595.030, 595.209, 610.021, 610.100, 650.055, and 650.457, RSMo, and to enact in lieu thereof forty-eight new sections relating to crime, with penalty provisions.




Be it enacted by the General Assembly of the state of Missouri, as follows:


              Section A. Sections 50.565, 192.925, 195.017, 195.217, 210.1012, 217.670, 217.690, 302.060, 304.230, 311.310, 311.325, 311.326, 409.5-508, 409.6-604, 479.260, 488.5025, 491.170, 545.050, 550.040, 559.021, 559.106, 561.031, 565.063, 565.081, 570.040, 573.037, 575.080, 575.150, 577.023, 577.500, 577.505, 578.250, 578.255, 578.260, 578.265, 590.190, 595.030, 595.209, 610.021, 610.100, 650.055, and 650.457, RSMo, are repealed and forty-eight new sections enacted in lieu thereof, to be known as sections 50.565, 192.925, 195.017, 195.217, 210.1012, 217.439, 217.670, 217.690, 302.060, 304.230, 311.310, 311.325, 311.326, 409.5-508, 409.6-604, 479.260, 488.5025, 488.5032, 491.170, 545.050, 550.040, 559.021, 559.106, 561.031, 565.063, 565.081, 570.040, 573.037, 575.075, 575.080, 575.150, 575.153, 577.023, 577.500, 577.505, 578.250, 578.255, 578.260, 578.265, 590.035, 590.190, 595.030, 595.209, 610.021, 610.100, 650.010, 650.055, and 650.457, to read as follows:

            50.565. 1. A county commission may establish by ordinance or order a fund whose proceeds may be expended only for the purposes provided for in subsection 3 of this section. The fund shall be designated as a county law enforcement restitution fund and shall be under the supervision of a board of trustees consisting of two citizens of the county appointed by the presiding commissioner of the county, two citizens of the county appointed by the sheriff of the county, and one citizen of the county appointed by the county coroner or medical examiner. The citizens so appointed shall not be current or former elected officials, current or former employees of the sheriff's department, the office of the prosecuting attorney for the county, office of the county commissioners, or the county treasurer's office. If a county does not have a coroner or medical examiner, the county treasurer shall appoint one citizen to the board of trustees.

            2. Money from the county law enforcement restitution fund shall only be expended upon the approval of a majority of the members of the county law enforcement restitution fund's board of trustees and only for the purposes provided for by subsection 3 of this section.

            3. Money from the county law enforcement restitution fund shall only be expended for the following purposes:

            (1) Narcotics investigation, prevention, and intervention;

            (2) Purchase of law enforcement-related equipment and supplies for the sheriff's office;

            (3) Matching funds for federal or state law enforcement grants;

            (4) Funding for the reporting of all state and federal crime statistics or information; and

            (5) Any county law enforcement-related expense, including those of the prosecuting attorney, approved by the board of trustees for the county law enforcement restitution fund that is reasonably related to investigation, charging, preparation, trial, and disposition of criminal cases before the courts of the state of Missouri.

            4. The county commission may not reduce any law enforcement agency's budget as a result of funds the law enforcement agency receives from the county law enforcement restitution fund. The restitution fund is to be used only as a supplement to the law enforcement agency's funding received from other county, state, or federal funds.

            5. County law enforcement restitution funds shall be audited as are all other county funds.

            6. No court may order the assessment and payment authorized by this section if the plea of guilty or the finding of guilt is to the charge of speeding, careless and imprudent driving, any charge of violating a traffic control signal or sign, or any charge which is a class C misdemeanor or an infraction, unless such charge is a moving violation, as defined by section 302.010, RSMo. No assessment and payment ordered pursuant to this section may exceed three hundred dollars for any charged offense.

            192.925. 1. To increase public awareness of the problem of elder abuse and neglect and financial exploitation of the elderly, the department of health and senior services shall implement an education and awareness program. Such program shall have the goal of reducing the incidences of elder abuse and neglect and financial exploitation of the elderly, and may focus on:

            (1) The education and awareness of mandatory reporters on their responsibility to report elder abuse and neglect and financial exploitation of the elderly;

            (2) Targeted education and awareness for the public on the problem, identification and reporting of elder abuse and neglect and financial exploitation of the elderly;

            (3) Publicizing the elder abuse and neglect hot line telephone number;

            (4) Education and awareness for law enforcement agencies and prosecutors on the problem and identification of elder abuse and neglect and financial exploitation of the elderly, and the importance of prosecuting cases pursuant to chapter 565, RSMo; and

            (5) Publicizing the availability of background checks prior to hiring an individual for caregiving purposes.

            2. The department of social services and facilities licensed pursuant to chapters 197 and 198, RSMo, shall cooperate fully with the department of health and senior services in the distribution of information pursuant to this program.

            195.017. 1. The department of health and senior services shall place a substance in Schedule I if it finds that the substance:

            (1) Has high potential for abuse; and

            (2) Has no accepted medical use in treatment in the United States or lacks accepted safety for use in treatment under medical supervision.

            2. Schedule I:

            (1) The controlled substances listed in this subsection are included in Schedule I;

            (2) Any of the following opiates, including their isomers, esters, ethers, salts, and salts of isomers, esters, and ethers, unless specifically excepted, whenever the existence of these isomers, esters, ethers and salts is possible within the specific chemical designation:

            (a) Acetyl-alpha-methylfentanyl;

            (b) Acetylmethadol;

            (c) Allylprodine;

            (d) Alphacetylmethadol;

            (e) Alphameprodine;

            (f) Alphamethadol;

            (g) Alpha-methylfentanyl;

            (h) Alpha-methylthiofentanyl;

            (i) Benzethidine;

            (j) Betacetylmethadol;

            (k) Beta-hydroxyfentanyl;

            (l) Beta-hydroxy-3-methylfentanyl;

            (m) Betameprodine;

            (n) Betamethadol;

            (o) Betaprodine;

            (p) Clonitazene;

            (q) Dextromoramide;

            (r) Diampromide;

            (s) Diethylthiambutene;

            (t) Difenoxin;

            (u) Dimenoxadol;

            (v) Dimepheptanol;

            (w) Dimethylthiambutene;

            (x) Dioxaphetyl butyrate;

            (y) Dipipanone;

            (z) Ethylmethylthiambutene;

            (aa) Etonitazene;

            (bb) Etoxeridine;

            (cc) Furethidine;

            (dd) Hydroxypethidine;

            (ee) Ketobemidone;

            (ff) Levomoramide;

            (gg) Levophenacylmorphan;

            (hh) 3-Methylfentanyl;

            (ii) 3-Methylthiofentanyl;

            (jj) Morpheridine;

            (kk) MPPP;

            (ll) Noracymethadol;

            (mm) Norlevorphanol;

            (nn) Normethadone;

            (oo) Norpipanone;

            (pp) Para-fluorofentanyl;

            (qq) PEPAP;

            (rr) Phenadoxone;

            (ss) Phenampromide;

            (tt) Phenomorphan;

            (uu) Phenoperidine;

            (vv) Piritramide;

            (ww) Proheptazine;

            (xx) Properidine;

            (yy) Propiram;

            (zz) Racemoramide;

            (aaa) Thiofentanyl;

            (bbb) Tilidine;

            (ccc) Trimeperidine;

            (3) Any of the following opium derivatives, their salts, isomers and salts of isomers unless specifically excepted, whenever the existence of these salts, isomers and salts of isomers is possible within the specific chemical designation:

            (a) Acetorphine;

            (b) Acetyldihydrocodeine;

            (c) Benzylmorphine;

            (d) Codeine methylbromide;

            (e) Codeine-N-Oxide;

            (f) Cyprenorphine;

            (g) Desomorphine;

            (h) Dihydromorphine;

            (i) Drotebanol;

            (j) Etorphine; (except Hydrochloride Salt);

            (k) Heroin;

            (l) Hydromorphinol;

            (m) Methyldesorphine;

            (n) Methyldihydromorphine;

            (o) Morphine methylbromide;

            (p) Morphine methyl sulfonate;

            (q) Morphine-N-Oxide;

            (r) [Morphine] Myrophine;

            (s) Nicocodeine;

            (t) Nicomorphine;

            (u) Normorphine;

            (v) Pholcodine;

            (w) Thebacon;

            (4) Any material, compound, mixture or preparation which contains any quantity of the following hallucinogenic substances, their salts, isomers and salts of isomers, unless specifically excepted, whenever the existence of these salts, isomers, and salts of isomers is possible within the specific chemical designation:

            (a) [4-brome-2] 4-bromo-2,5-dimethoxyamphetamine;

            (b) 4-bromo-2, 5-dimethoxyphenethylamine;

            (c) 2,5-dimethoxyamphetamine;

            (d) 2,5-dimethoxy-4-ethylamphetamine;

            (e) 2,5-dimethoxy-4-(n)-propylthiophenethylamine;

            (f) 4-methoxyamphetamine;

            (g) 5-methoxy-3,4-methylenedioxyamphetamine;

            (h) 4-methyl-2,5-dimethoxy amphetamine;

            (i) 3,4-methylenedioxyamphetamine;

            (j) 3,4-methylenedioxymethamphetamine;

            (k) 3,4-methylenedioxy-N-ethylamphetamine;

            (l) [N-nydroxy-3] N-hydroxy-3, 4-methylenedioxyamphetamine;

            (m) 3,4,5-trimethoxyamphetamine;

            (n) Alpha-ethyltryptamine;

            (o) Benzylpiperazine or B.P.;

            (p) Bufotenine;

            (q) Diethyltryptamine;

            (r) Dimethyltryptamine;

            (s) Ibogaine;

            (t) Lysergic acid diethylamide;

            (u) Marijuana; (Marihuana);

            (v) Mescaline;

            (w) Parahexyl;

            (x) Peyote, to include all parts of the plant presently classified botanically as Lophophora Williamsil Lemaire, whether growing or not; the seeds thereof; any extract from any part of such plant; and every compound, manufacture, salt, derivative, mixture or preparation of the plant, its seed or extracts;

            (y) N-ethyl-3-piperidyl benzilate;

            (z) N-methyl-3-piperidyl benzilate;

            (aa) Psilocybin;

            (bb) Psilocyn;

            (cc) Tetrahydrocannabinols;

            (dd) Ethylamine analog of phencyclidine;

            (ee) Pyrrolidine analog of phencyclidine;

            (ff) Thiophene analog of phencyclidine;

            (gg) 1-(3-Trifluoromethylphenyl)piperazine or TFMPP;

            (hh) 1-(1-(2-thienyl)cyclohexyl) pyrrolidine;

            (ii) Salvia divinorum;

            (jj) Salvinorin A;

            (5) Any material, compound, mixture or preparation containing any quantity of the following substances having a depressant effect on the central nervous system, including their salts, isomers and salts of isomers whenever the existence of these salts, isomers and salts of isomers is possible within the specific chemical designation:

            (a) Gamma hydroxybutyric acid;

            (b) Mecloqualone;

            (c) Methaqualone;

            (6) Any material, compound, mixture or preparation containing any quantity of the following substances having a stimulant effect on the central nervous system, including their salts, isomers and salts of isomers:

            (a) Aminorex;

            (b) Cathinone;

            (c) Fenethylline;

            (d) Methcathinone;

            (e) (+)cis-4-methylaminorex ((+)cis-4,5-dihydro- 4-methyl-5-phenyl-2-oxazolamine);

            (f) N-ethylamphetamine;

            (g) N,N-dimethylamphetamine;

            (7) A temporary listing of substances subject to emergency scheduling under federal law shall include any material, compound, mixture or preparation which contains any quantity of the following substances:

            (a) N-(1-benzyl-4-piperidyl)-N-phenyl-propanamide (benzylfentanyl), its optical isomers, salts and salts of isomers;

            (b) N-(1-(2-thienyl)methyl-4-piperidyl)-N-phenylpropanamide (thenylfentanyl), its optical isomers, salts and salts of isomers;

            (c) Alpha-Methyltryptamine, or (AMT);

            (d) 5-Methoxy-N,N-Diisopropyltryptamine, or(5-MeO-DIPT);

            (8) Khat, to include all parts of the plant presently classified botanically as catha edulis, whether growing or not; the seeds thereof; any extract from any part of such plant; and every compound, manufacture, salt, derivative, mixture, or preparation of the plant, its seed or extracts.

            3. The department of health and senior services shall place a substance in Schedule II if it finds that:

            (1) The substance has high potential for abuse;

            (2) The substance has currently accepted medical use in treatment in the United States, or currently accepted medical use with severe restrictions; and

            (3) The abuse of the substance may lead to severe psychic or physical dependence.

            4. The controlled substances listed in this subsection are included in Schedule II:

            (1) Any of the following substances whether produced directly or indirectly by extraction from substances of vegetable origin, or independently by means of chemical synthesis, or by combination of extraction and chemical synthesis:

            (a) Opium and opiate and any salt, compound, derivative or preparation of opium or opiate, excluding apomorphine, thebaine-derived butorphanol, dextrorphan, nalbuphine, nalmefene, naloxone and naltrexone, and their respective salts but including the following:

            a. Raw opium;

            b. Opium extracts;

            c. Opium fluid;

            d. Powdered opium;

            e. Granulated opium;

            f. Tincture of opium;

            g. Codeine;

            h. Ethylmorphine;

            i. Etorphine hydrochloride;

            j. Hydrocodone;

            k. Hydromorphone;

            l. Metopon;

            m. Morphine;

            n. Oxycodone;

            o. Oxymorphone;

            p. Thebaine;

            (b) Any salt, compound, derivative, or preparation thereof which is chemically equivalent or identical with any of the substances referred to in this subdivision, but not including the isoquinoline alkaloids of opium;

            (c) Opium poppy and poppy straw;

            (d) Coca leaves and any salt, compound, derivative, or preparation of coca leaves, and any salt, compound, derivative, or preparation thereof which is chemically equivalent or identical with any of these substances, but not including decocainized coca leaves or extractions which do not contain cocaine or ecgonine;

            (e) Concentrate of poppy straw (the crude extract of poppy straw in either liquid, solid or powder form which contains the phenanthrene alkaloids of the opium poppy);

            (2) Any of the following opiates, including their isomers, esters, ethers, salts, and salts of isomers, whenever the existence of these isomers, esters, ethers and salts is possible within the specific chemical designation, dextrorphan and levopropoxyphene excepted:

            (a) Alfentanil;

            (b) Alphaprodine;

            (c) Anileridine;

            (d) Bezitramide;

            (e) Bulk Dextropropoxyphene;

            (f) Carfentanil;

            (g) Butyl nitrite;

            (h) Dihydrocodeine;

            (i) Diphenoxylate;

            (j) Fentanyl;

            (k) Isomethadone;

            (l) Levo-alphacetylmethadol;

            (m) Levomethorphan;

            (n) Levorphanol;

            (o) Metazocine;

            (p) Methadone;

            (q) Meperidine;

            (r) Methadone-Intermediate, 4-cyano-2-dimethylamino-4, 4-diphenylbutane;

            (s) Moramide-Intermediate, 2-methyl-3-morpholino-1, 1-diphenylpropane--carboxylic acid;

            (t) Pethidine;

            (u) Pethidine-Intermediate-A, 4-cyano-1-methyl-4-phenylpiperidine;

            (v) Pethidine-Intermediate-B, ethyl-4-phenylpiperidine-4-carboxylate;

            (w) Pethidine-Intermediate-C, 1-methyl-4-phenylpiperdine-4-carboxylic acid;

            (x) Phenazocine;

            (y) Piminodine;

            (z) Racemethorphan;

            (aa) Racemorphan;

            (bb) Sufentanil;

            (3) Any material, compound, mixture, or preparation which contains any quantity of the following substances having a stimulant effect on the central nervous system:

            (a) Amphetamine, its salts, optical isomers, and salts of its optical isomers;

            (b) Methamphetamine, its salts, isomers, and salts of its isomers;

            (c) Phenmetrazine and its salts;

            (d) Methylphenidate;

            (4) Any material, compound, mixture, or preparation which contains any quantity of the following substances having a depressant effect on the central nervous system, including its salts, isomers, and salts of isomers whenever the existence of those salts, isomers, and salts of isomers is possible within the specific chemical designation:

            (a) Amobarbital;

            (b) Glutethimide;

            (c) Pentobarbital;

            (d) Phencyclidine;

            (e) Secobarbital;

            (5) Any material, compound or compound which contains any quantity of nabilone;

            (6) Any material, compound, mixture, or preparation which contains any quantity of the following substances:

            (a) Immediate precursor to amphetamine and methamphetamine: Phenylacetone;

            (b) Immediate precursors to phencyclidine (PCP):

            a. 1-phenylcyclohexylamine;

            b. 1-piperidinocyclohexanecarbonitrile (PCC).

            5. The department of health and senior services shall place a substance in Schedule III if it finds that:

            (1) The substance has a potential for abuse less than the substances listed in Schedules I and II;

            (2) The substance has currently accepted medical use in treatment in the United States; and

            (3) Abuse of the substance may lead to moderate or low physical dependence or high psychological dependence.

            6. The controlled substances listed in this subsection are included in Schedule III:

            (1) Any material, compound, mixture, or preparation which contains any quantity of the following substances having a potential for abuse associated with a stimulant effect on the central nervous system:

            (a) Benzphetamine;

            (b) Chlorphentermine;

            (c) Clortermine;

            (d) Phendimetrazine;

            (2) Any material, compound, mixture or preparation which contains any quantity or salt of the following substances or salts having a depressant effect on the central nervous system:

            (a) Any material, compound, mixture or preparation which contains any quantity or salt of the following substances combined with one or more active medicinal ingredients:

            a. Amobarbital;

            b. Gamma hydroxybutyric acid and its salts, isomers, and salts of isomers contained in a drug product for which an application has been approved under Section 505 of the Federal Food, Drug, and Cosmetic Act;

            c. Secobarbital;

            d. Pentobarbital;

            (b) Any suppository dosage form containing any quantity or salt of the following:

            a. Amobarbital;

            b. Secobarbital;

            c. Pentobarbital;

            (c) Any substance which contains any quantity of a derivative of barbituric acid or its salt;

            (d) Chlorhexadol;

            (e) Ketamine, its salts, isomers, and salts of isomers;

            (f) Lysergic acid;

            (g) Lysergic acid amide;

            (h) Methyprylon;

            (i) Sulfondiethylmethane;

            (j) Sulfonethylmethane;

            (k) Sulfonmethane;

            (l) Tiletamine and zolazepam or any salt thereof;

            (3) Nalorphine;

            (4) Any material, compound, mixture, or preparation containing limited quantities of any of the following narcotic drugs or their salts:

            (a) Not more than 1.8 grams of codeine per one hundred milliliters or not more than ninety milligrams per dosage unit, with an equal or greater quantity of an isoquinoline alkaloid of opium;

            (b) Not more than 1.8 grams of codeine per one hundred milliliters or not more than ninety milligrams per dosage unit with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;

            (c) Not more than three hundred milligrams of hydrocodone per one hundred milliliters or not more than fifteen milligrams per dosage unit, with a fourfold or greater quantity of an isoquinoline alkaloid of opium;

            (d) Not more than three hundred milligrams of hydrocodone per one hundred milliliters or not more than fifteen milligrams per dosage unit, with one or more active nonnarcotic ingredients in recognized therapeutic amounts;

            (e) Not more than 1.8 grams of dihydrocodeine per one hundred milliliters or more than ninety milligrams per dosage unit, with one or more active nonnarcotic ingredients in recognized therapeutic amounts;

            (f) Not more than three hundred milligrams of ethylmorphine per one hundred milliliters or not more than fifteen milligrams per dosage unit, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;

            (g) Not more than five hundred milligrams of opium per one hundred milliliters or per one hundred grams or not more than twenty-five milligrams per dosage unit, with one or more active nonnarcotic ingredients in recognized therapeutic amounts;

            (h) Not more than fifty milligrams of morphine per one hundred milliliters or per one hundred grams, with one or more active, nonnarcotic ingredients in recognized therapeutic amounts;

            (5) Any material, compound, mixture, or preparation containing any of the following narcotic drugs or their salts, as set forth in subdivision (6) of this subsection; buprenorphine;

            (6) Anabolic steroids. Any drug or hormonal substance, chemically and pharmacologically related to testosterone (other than estrogens, progestins, and corticosteroids) that promotes muscle growth, except an anabolic steroid which is expressly intended for administration through implants to cattle or other nonhuman species and which has been approved by the Secretary of Health and Human Services for that administration. If any person prescribes, dispenses, or distributes such steroid for human use, such person shall be considered to have prescribed, dispensed, or distributed an anabolic steroid within the meaning of this paragraph. Unless specifically excepted or unless listed in another schedule, any material, compound, mixture or preparation containing any quantity of the following substances, including its salts, isomers and salts of isomers whenever the existence of such salts of isomers is possible within the specific chemical designation:

            (a) Boldenone;

            (b) Chlorotestosterone (4-Chlortestosterone);

            (c) Clostebol;

            (d) Dehydrochlormethyltestosterone;

            (e) Dihydrostestosterone (4-Dihydro-testosterone);

            (f) Drostanolone;

            (g) Ethylestrenol;

            (h) Fluoxymesterone;

            (i) Formebulone (Formebolone);

            (j) Mesterolone;

            (k) Methandienone;

            (l) Methandranone;

            (m) Methandriol;

            (n) Methandrostenolone;

            (o) Methenolone;

            (p) Methyltestosterone;

            (q) Mibolerone;

            (r) Nandrolone;

            (s) Norethandrolone;

            (t) Oxandrolone;

            (u) Oxymesterone;

            (v) Oxymetholone;

            (w) Stanolone;

            (x) Stanozolol;

            (y) Testolactone;

            (z) Testosterone;

            (aa) Trenbolone;

            (bb) Any salt, ester, or isomer of a drug or substance described or listed in this subdivision, if that salt, ester or isomer promotes muscle growth except an anabolic steroid which is expressly intended for administration through implants to cattle or other nonhuman species and which has been approved by the Secretary of Health and Human Services for that administration;

            (7) Dronabinol (synthetic) in sesame oil and encapsulated in a soft gelatin capsule in a United States Food and Drug Administration approved drug product. Some other names for dronabinol: (6aR-trans)-6a,7,8,10a- tetrahydro-6.6.9-trimethyl-3-pentyl-6H-dibenzo (b,d) pyran-1-ol, or (-)- delta-9-(trans)-tetrahydracannabinol);

            (8) The department of health and senior services may except by rule any compound, mixture, or preparation containing any stimulant or depressant substance listed in subdivisions (1) and (2) of this subsection from the application of all or any part of sections 195.010 to 195.320 if the compound, mixture, or preparation contains one or more active medicinal ingredients not having a stimulant or depressant effect on the central nervous system, and if the admixtures are included therein in combinations, quantity, proportion, or concentration that vitiate the potential for abuse of the substances which have a stimulant or depressant effect on the central nervous system.

            7. The department of health and senior services shall place a substance in Schedule IV if it finds that:

            (1) The substance has a low potential for abuse relative to substances in Schedule III;

            (2) The substance has currently accepted medical use in treatment in the United States; and

            (3) Abuse of the substance may lead to limited physical dependence or psychological dependence relative to the substances in Schedule III.

            8. The controlled substances listed in this subsection are included in Schedule IV:

            (1) Any material, compound, mixture, or preparation containing any of the following narcotic drugs or their salts calculated as the free anhydrous base or alkaloid, in limited quantities as set forth below:

            (a) Not more than one milligram of difenoxin and not less than twenty-five micrograms of atropine sulfate per dosage unit;

            (b) Dextropropoxyphene (alpha-(+)-4-dimethy-lamino-1, 2-diphenyl-3-methyl-2- propionoxybutane);

            (c) Any of the following limited quantities of narcotic drugs or their salts, which shall include one or more nonnarcotic active medicinal ingredients in sufficient proportion to confer upon the compound, mixture or preparation valuable medicinal qualities other than those possessed by the narcotic drug alone:

            a. Not more than two hundred milligrams of codeine per one hundred milliliters or per one hundred grams;

            b. Not more than one hundred milligrams of dihydrocodeine per one hundred milliliters or per one hundred grams;

            c. Not more than one hundred milligrams of ethylmorphine per one hundred milliliters or per one hundred grams;

            (2) Any material, compound, mixture or preparation containing any quantity of the following substances, including their salts, isomers, and salts of isomers whenever the existence of those salts, isomers, and salts of isomers is possible within the specific chemical designation:

            (a) Alprazolam;

            (b) Barbital;

            (c) Bromazepam;

            (d) Camazepam;

            (e) Chloral betaine;

            (f) Chloral hydrate;

            (g) Chlordiazepoxide;

            (h) Clobazam;

            (i) Clonazepam;

            (j) Clorazepate;

            (k) Clotiazepam;

            (l) Cloxazolam;

            (m) Delorazepam;

            (n) Diazepam;

            (o) Dichloralphenazone;

            (p) Estazolam;

            (q) Ethchlorvynol;

            (r) Ethinamate;

            (s) Ethyl loflazepate;

            (t) Fludiazepam;

            (u) Flunitrazepam;

            (v) Flurazepam;

            (w) Halazepam;

            (x) Haloxazolam;

            (y) Ketazolam;

            (z) Loprazolam;

            (aa) Lorazepam;

            (bb) Lormetazepam;

            (cc) Mebutamate;

            (dd) Medazepam;

            (ee) Meprobamate;

            (ff) Methohexital;

            (gg) Methylphenobarbital;

            (hh) Midazolam;

            (ii) Nimetazepam;

            (jj) Nitrazepam;

            (kk) Nordiazepam;

            (ll) Oxazepam;

            (mm) Oxazolam;

            (nn) Paraldehyde;

            (oo) Petrichloral;

            (pp) Phenobarbital;

            (qq) Pinazepam;

            (rr) Prazepam;

            (ss) Quazepam;

            (tt) Temazepam;

            (uu) Tetrazepam;

            (vv) Triazolam;

            (ww) Zaleplon;

            (xx) Zolpidem;

            (yy) Zopiclone, including its salts, isomers, and salts of isomers;

            (3) Any material, compound, mixture, or preparation which contains any quantity of the following substance including its salts, isomers and salts of isomers whenever the existence of such salts, isomers and salts of isomers is possible: fenfluramine;

            (4) Any material, compound, mixture or preparation containing any quantity of the following substances having a stimulant effect on the central nervous system, including their salts, isomers and salts of isomers:

            (a) Cathine ((+)-norpseudoephedrine);

            (b) Diethylpropion;

            (c) Fencamfamin;

            (d) Fenproporex;

            (e) Mazindol;

            (f) Mefenorex;

            (g) Modafinil;

            (h) Pemoline, including organometallic complexes and chelates thereof;

            (i) Phentermine;

            (j) Pipradrol;

            (k) Sibutramine;

            (l) SPA ((-)-1-dimethyamino-1,2-diphenylethane);

            (5) Any material, compound, mixture or preparation containing any quantity of the following substance, including its salts:

            (a) butorphanol;

            (b) pentazocine;

            (6) Ephedrine, its salts, optical isomers and salts of optical isomers, when the substance is the only active medicinal ingredient;

            (7) The department of health and senior services may except by rule any compound, mixture, or preparation containing any depressant substance listed in subdivision (1) of this subsection from the application of all or any part of sections 195.010 to 195.320 if the compound, mixture, or preparation contains one or more active medicinal ingredients not having a depressant effect on the central nervous system, and if the admixtures are included therein in combinations, quantity, proportion, or concentration that vitiate the potential for abuse of the substances which have a depressant effect on the central nervous system.

            9. The department of health and senior services shall place a substance in Schedule V if it finds that:

            (1) The substance has low potential for abuse relative to the controlled substances listed in Schedule IV;

            (2) The substance has currently accepted medical use in treatment in the United States; and

            (3) The substance has limited physical dependence or psychological dependence liability relative to the controlled substances listed in Schedule IV.

            10. The controlled substances listed in this subsection are included in Schedule V:

            (1) Any compound, mixture or preparation containing any of the following narcotic drugs or their salts calculated as the free anhydrous base or alkaloid, in limited quantities as set forth below, which also contains one or more nonnarcotic active medicinal ingredients in sufficient proportion to confer upon the compound, mixture or preparation valuable medicinal qualities other than those possessed by the narcotic drug alone:

            (a) Not more than two and five-tenths milligrams of diphenoxylate and not less than twenty-five micrograms of atropine sulfate per dosage unit;

            (b) Not more than one hundred milligrams of opium per one hundred milliliters or per one hundred grams;

            (c) Not more than five-tenths milligram of difenoxin and not less than twenty-five micrograms of atropine sulfate per dosage unit;

            (2) Any material, compound, mixture or preparation which contains any quantity of the following substance having a stimulant effect on the central nervous system including its salts, isomers and salts of isomers: pyrovalerone;

            (3) Any compound, mixture, or preparation containing any detectable quantity of pseudoephedrine or its salts or optical isomers, or salts of optical isomers or any compound, mixture, or preparation containing any detectable quantity of ephedrine or its salts or optical isomers, or salts of optical isomers;

            (4) Depressants. Unless specifically exempted or excluded or unless listed in another schedule, any material, compound, mixture, or preparation which contains any quantity of the following substances having a depressant effect on the central nervous system, including its salts:

            (a) Pregabalin ( (S)-3 (aminomethyl) - 5 - methylhexanoic acid).

            11. If any compound, mixture, or preparation as specified in subdivision (3) of subsection 10 of this section is dispensed, sold, or distributed in a pharmacy without a prescription:

            (1) All packages of any compound, mixture, or preparation containing any detectable quantity of pseudoephedrine, its salts or optical isomers, or salts of optical isomers or ephedrine, its salts or optical isomers, or salts of optical isomers, shall be offered for sale only from behind a pharmacy counter where the public is not permitted, and only by a registered pharmacist or registered pharmacy technician; and

            (2) Any person purchasing, receiving or otherwise acquiring any compound, mixture, or preparation containing any detectable quantity of pseudoephedrine, its salts or optical isomers, or salts of optical isomers or ephedrine, its salts or optical isomers, or salts of optical isomers shall be at least eighteen years of age; and

            (3) The pharmacist or registered pharmacy technician shall require any person purchasing, receiving or otherwise acquiring such compound, mixture, or preparation, who is not known to the pharmacist or registered pharmacy technician, to furnish suitable photo identification showing the date of birth of the person.

            12. Within ninety days of the enactment of this section, pharmacists and registered pharmacy technicians shall implement and maintain a written or electronic log of each transaction. Such log shall include the following information:

            (1) The name and address of the purchaser;

            (2) The amount of the compound, mixture, or preparation purchased;

            (3) The date of each purchase; and

            (4) The name or initials of the pharmacist or registered pharmacy technician who dispensed the compound, mixture, or preparation to the purchaser.

            13. No person shall dispense, sell, purchase, receive, or otherwise acquire quantities greater than those specified in this chapter.

            14. Within thirty days of the enactment of this section, all persons who dispense or offer for sale pseudoephedrine and ephedrine products in a pharmacy shall ensure that all such products are located only behind a pharmacy counter where the public is not permitted.

            15. Within thirty days of the enactment of this section, any business entity which sells ephedrine or pseudoephedrine products in the course of legitimate business which is in the possession of pseudoephedrine and ephedrine products, and which does not have a state and federal controlled substances registration, shall return these products to a manufacturer or distributor or transfer them to an authorized controlled substances registrant.

            16. Any person who knowingly or recklessly violates the provisions of subsections 11 to 15 of this section is guilty of a class A misdemeanor.

            17. The scheduling of substances specified in subdivision (3) of subsection 10 of this section and subsections 11, 12, 14, and 15 of this section shall not apply to any compounds, mixtures, or preparations that are in liquid or liquid-filled gel capsule form or to any compound, mixture, or preparation specified in subdivision (3) of subsection 10 of this section which must be dispensed, sold, or distributed in a pharmacy pursuant to a prescription.

            18. The manufacturer of a drug product or another interested party may apply with the department of health and senior services for an exemption from this section. The department of health and senior services may grant an exemption by rule from this section if the department finds the drug product is not used in the illegal manufacture of methamphetamine or other controlled or dangerous substances. The department of health and senior services shall rely on reports from law enforcement and law enforcement evidentiary laboratories in determining if the proposed product can be used to manufacture illicit controlled substances.

            19. The department of health and senior services shall revise and republish the schedules annually.

            20. The department of health and senior services shall promulgate rules under chapter 536, RSMo, regarding the security and storage of Schedule V controlled substances, as described in subdivision (3) of subsection 10 of this section, for distributors as registered by the department of health and senior services.

            195.217. 1. A person commits the offense of distribution of a controlled substance near a park if such person violates section 195.211 by unlawfully distributing or delivering [heroin, cocaine, LSD, amphetamine, or methamphetamine] any controlled substance to a person in or on, or within one thousand feet of, the real property comprising a public or private park, state park, county park, or municipal park [or a public or private park designed for public recreational purposes, as park is defined in section 253.010, RSMo].

            2. Distribution of a controlled substance near a park is a class A felony.

            210.1012. 1. There is hereby created a statewide program called the "Amber Alert System" referred to in this section as the "system" to aid in the identification and location of an abducted child.

            2. For the purposes of this section, "abducted child" means a child whose whereabouts are unknown and who is:

            (1) Less than eighteen years of age and reasonably believed to be the victim of the crime of kidnapping as defined by section 565.110, RSMo, as determined by local law enforcement;

            (2) Reasonably believed to be the victim of the crime of child kidnapping as defined by section 565.115, RSMo, as determined by [local] law enforcement; or

            (3) Less than eighteen years of age and at least fourteen years of age, and who[, if under the age of fourteen,] would otherwise be reasonably believed to be a victim of child kidnapping as defined by section 565.115, RSMo, as determined by [local] law enforcement, if such person was under the age of fourteen.

            3. The department of public safety shall develop regions to provide the system. The department of public safety shall coordinate local law enforcement agencies and public commercial television and radio broadcasters to provide an effective system. In the event that a local law enforcement agency opts not to set up a system and an abduction occurs within the jurisdiction, it shall notify the department of public safety who will notify local media in the region.

            4. The Amber alert system shall include all state agencies capable of providing urgent and timely information to the public together with broadcasters and other private entities that volunteer to participate in the dissemination of urgent public information. At a minimum, the Amber alert system shall include the department of public safety, highway patrol, department of transportation, department of health and senior services, and Missouri lottery.

            5. The department of public safety shall have the authority to notify other regions upon verification that the criteria established by the oversight committee has been met.

            6. Participation in an Amber alert system is entirely at the option of local law enforcement agencies and federally licensed radio and television broadcasters.

            7. Any person who knowingly makes a false report that triggers an alert pursuant to this section is guilty of a class A misdemeanor.

            217.439. Upon the victim's request, a photograph shall be taken of the incarcerated individual prior to release from incarceration and a copy of the photograph shall be provided to the crime victim.

            217.670. 1. The board shall adopt an official seal of which the courts shall take official notice.

            2. Decisions of the board regarding granting of paroles, extensions of a conditional release date or revocations of a parole or conditional release shall be by a majority vote of the hearing panel members. The hearing panel shall consist of one member of the board and two hearing officers appointed by the board. A member of the board may remove the case from the jurisdiction of the hearing panel and refer it to the full board for a decision. Within thirty days of entry of the decision of the hearing panel to deny parole or to revoke a parole or conditional release, the offender may appeal the decision of the hearing panel to the board. The board shall consider the appeal within thirty days of receipt of the appeal. The decision of the board shall be by majority vote of the board members and shall be final.

            3. The orders of the board shall not be reviewable except as to compliance with the terms of sections 217.650 to 217.810 or any rules promulgated pursuant to such section.

            4. The board shall keep a record of its acts and shall notify each correctional center of its decisions relating to persons who are or have been confined in such correctional center.

            5. Notwithstanding any other provision of law, any meeting, record, or vote, of proceedings involving probation, parole, or pardon, may be a closed meeting, closed record, or closed vote.

            6. Notwithstanding any other provision of law to the contrary, when the appearance or presence of an offender before the board or a hearing panel is required for the purpose of deciding whether to grant conditional release or parole, extending the date of conditional release, revoking parole or conditional release, or for any other purpose, such appearance or presence may occur by means of a video conference at the discretion of the board. Victims having a right to attend such hearings may testify either at the site where the board is conducting the video conference or at the institution where the offender is located.

            217.690. 1. When in its opinion there is reasonable probability that an offender of a correctional center can be released without detriment to the community or to himself, the board may in its discretion release or parole such person except as otherwise prohibited by law. All paroles shall issue upon order of the board, duly adopted.

            2. Before ordering the parole of any offender, the board shall have the offender appear before a hearing panel and shall conduct a personal interview with him, unless waived by the offender. A parole shall be ordered only for the best interest of society, not as an award of clemency; it shall not be considered a reduction of sentence or a pardon. An offender shall be placed on parole only when the board believes that he is able and willing to fulfill the obligations of a law-abiding citizen. Every offender while on parole shall remain in the legal custody of the department but shall be subject to the orders of the board.

            3. The board has discretionary authority to require the payment of a fee, not to exceed sixty dollars per month, from every offender placed under board supervision on probation, parole, or conditional release, to waive all or part of any fee, to sanction offenders for willful nonpayment of fees, and to contract with a private entity for fee collections services. All fees collected shall be deposited in the inmate fund established in section 217.430. Fees collected may be used to pay the costs of contracted collections services. The fees collected may otherwise be used to provide community corrections and intervention services for offenders. Such services include substance abuse assessment and treatment, mental health assessment and treatment, electronic monitoring services, residential facilities services, employment placement services, and other offender community corrections or intervention services designated by the board to assist offenders to successfully complete probation, parole, or conditional release. The board shall adopt rules not inconsistent with law, in accordance with section 217.040, with respect to sanctioning offenders and with respect to establishing, waiving, collecting, and using fees.

            4. The board shall adopt rules not inconsistent with law, in accordance with section 217.040, with respect to the eligibility of offenders for parole, the conduct of parole hearings or conditions to be imposed upon paroled offenders. Whenever an order for parole is issued it shall recite the conditions of such parole.

            5. When considering parole for an offender with consecutive sentences, the minimum term for eligibility for parole shall be calculated by adding the minimum terms for parole eligibility for each of the consecutive sentences, except the minimum term for parole eligibility shall not exceed the minimum term for parole eligibility for an ordinary life sentence.

            6. Any offender under a sentence for first degree murder who has been denied release on parole after a parole hearing shall not be eligible for another parole hearing until at least three years from the month of the parole denial; however, this subsection shall not prevent a release pursuant to subsection 4 of section 558.011, RSMo.

            7. Parole hearings shall, at a minimum, contain the following procedures:

            (1) The victim or person representing the victim who attends a hearing may be accompanied by one other person;

            (2) The victim or person representing the victim who attends a hearing shall have the option of giving testimony in the presence of the inmate or to the hearing panel without the inmate being present;

            (3) The victim or person representing the victim may call or write the parole board rather than attend the hearing;

            (4) The victim or person representing the victim may have a personal meeting with a board member at the board's central office;

            (5) The judge, prosecuting attorney or circuit attorney and a representative of the local law enforcement agency investigating the crime shall be allowed to attend the hearing or provide information to the hearing panel in regard to the parole consideration; and

            (6) The board shall evaluate information listed in the juvenile sex offender registry pursuant to section 211.425, RSMo, provided the offender is between the ages of seventeen and twenty-one, as it impacts the safety of the community.

            8. The board shall notify any person of the results of a parole eligibility hearing if the person indicates to the board a desire to be notified.

            9. The board may, at its discretion, require any offender seeking parole to meet certain conditions during the term of that parole so long as said conditions are not illegal or impossible for the offender to perform. These conditions may include an amount of restitution to the state for the cost of that offender's incarceration. These conditions may also include the performance of a designated amount of free work for a public or charitable purpose as determined by the board.

            (1) An offender may refuse parole that is conditioned on the performance of free work. In such cases, the board shall take that fact into account when