Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005
Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005
Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005: revoked, on 1 November 2011, pursuant to regulation 16 of the Agricultural Compounds and Veterinary Medicines (Exemptions and Prohibited Substances) Regulations 2011 (SR 2011/327).
Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005
Reprint
as at 1 November 2011
Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005
(SR 2005/90)
Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005: revoked, on 1 November 2011, pursuant to regulation 16 of the Agricultural Compounds and Veterinary Medicines (Exemptions and Prohibited Substances) Regulations 2011 (SR 2011/327).
Note
Changes authorised by section 17C of the Acts and Regulations Publication Act 1989 have been made in this eprint.
A general outline of these changes is set out in the notes at the end of this eprint, together with other explanatory material about this eprint.
These regulations are administered by the Ministry of Agriculture and Forestry.
Pursuant to section 75 of the Agricultural Compounds and Veterinary Medicines Act 1997, Her Excellency the Governor-General, acting on the advice and with the consent of the Executive Council, makes the following regulations.
Contents
3 Agricultural compounds exempt from registration if conditions complied with
7 New Schedules 1 to 4 substituted
Schedule 1
New Schedules 1 to 4 substituted in principal regulations
Schedule 2
New Schedule 7 substituted in principal regulations
1 Title
-
(1) These regulations are the Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005.
(2) In these regulations, the Agricultural Compounds and Veterinary Medicines Regulations 20011 are called
“the principal regulations”
.
2 Commencement
These regulations come into force on the 28th day after the date of their notification in the Gazette.
3 Agricultural compounds exempt from registration if conditions complied with
-
(1) Regulation 5 of the principal regulations is amended by omitting the words
“Schedules 2 and 3”
, and substituting the expression“Schedule 2”
.(2) Regulation 5(b) of the principal regulations is amended by omitting the word
“schedules”
, and substituting the word“schedule”
.
4 New regulation 5A inserted
The principal regulations are amended by inserting, after regulation 5, the following regulation:
“5A Combined agricultural compounds exempt from registration
-
“(1) An agricultural compound is exempt from registration under section 21 or section 27 of the Act if the agricultural compound is a combination of 2 or more agricultural compounds that are exempt from registration under these regulations.
“(2) The combined agricultural compound is subject to any—
“(a) conditions set out in column 2 of Schedule 2; and
“(b) other provision of these regulations that applies to each agricultural compound that comprises the combined agricultural compound.”
-
5 Information requirements
-
(1) Regulation 6 of the principal regulations is amended by omitting the words
“Schedules 2 and 3”
, and substituting the expression“Schedule 2”
.(2) Regulation 6(f) of the principal regulations is amended by omitting the words
“or Schedule 3”
.
6 Regulation 7 revoked
Regulation 7 of the principal regulations is revoked.
7 New Schedules 1 to 4 substituted
The principal regulations are amended by revoking Schedules 1, 2, 3, and 4 and substituting the Schedules 1, 2, 3, and 4 set out in Schedule 1 of these regulations.
8 New Schedule 7 substituted
The principal regulations are amended by revoking Schedule 7, and substituting the Schedule 7 set out in Schedule 2 of these regulations.
Schedule 1 |
Schedule 1
Agricultural compounds exempt from registration under sections 21 and 27 of Act if applicable codes of practice complied withr 4
1 Compounds (including homeopathic, herbal, chemical, and oral nutritional compounds) prepared by a person for use by the person as an agricultural compound on animals or plants owned by the person, or in any land, place, or water owned or occupied by the person. The following compounds are excluded unless there is an applicable code of practice in force under section 28 of the Act: (a) active ingredients that are prescription medicines or restricted medicines (as those terms are defined in the Medicines Act 1981): (b) antibiotic active ingredients: (c) hormones: (d) substances that are prohibited by countries importing New Zealand primary produce: (e) vertebrate toxic agents. 2 Homeopathic plant compounds used commercially. 3 Non-medicated topical hoof preparations used solely to maintain or improve hoof condition. 4 Non-medicated topical skin preparations used solely to maintain or improve skin condition. 5 Non-absorbent masking agents used to disguise odours. 6 Topical non-absorbent and non-solvent cleaning products, including non-medicated shampoos, soaps, tear-stain removers, and toothpaste. 7 In vitro diagnostics used to confirm the presence or absence of disease or as an aid in the diagnosis of disease or abnormal conditions. 8 Compounds used in the production of plant tissue cultures. 9 Compounds (not containing biologically active ingredients) used to protect plant grafts. 10 Vertebrate and invertebrate attractants and repellants that are not applied directly to animals or plants. 11 Invertebrate mating disrupters that are not applied directly to animals or plants. 12 Antisapstains. 13 A preparation of 2 or more ingredients if each ingredient is an agricultural compound described in this schedule and the combination of ingredients does not increase or change any of the risks described in section 19 of the Act.
Schedule 2
Agricultural compounds exempt from registration under sections 21 and 27 of Act if conditions in column 2 and requirements in regulation 6 complied withrr 5, 6
Column 1 Column 2 Agricultural compound Conditions Oral and topical preparations— If used as a veterinary medicine, the label information must— (a) prepared by a process of solution, extraction, or titration of an active ingredient followed by strictly regimented serial dilution; and (a) identify the compound as a homeopathic preparation; and (b) that do not claim to prevent, control, or cure a specific disease characterised by pain or distress in animals (b) include a statement that, if the preparation fails to alleviate the condition being treated, the user should seek veterinary advice Oral and topical preparations— If used as a veterinary medicine, the label information must— (a) prepared from either any part of a plant or an unrefined extract from a plant, except a plant listed in Schedule 6; and (a) identify the compound as a herbal preparation; and (b) that do not claim to prevent, control, or cure a specific disease characterised by pain or distress in animals (b) include a statement that, if the preparation fails to alleviate the condition being treated, the user should seek veterinary advice Must not be used on the teats of lactating animals if the milk of the animals is intended for human consumption Markers, paints, and dyes used as pigments or colourants for topical application to identify animals temporarily Over the counter first aid preparations, including general disinfectants, antiseptics, and sanitisers Must not be used on the teats of lactating animals if the milk of the animals is intended for human consumption Preparations scheduled as pharmacy only, prescription, or restricted medicines under the Medicines Act 1981, used as veterinary medicines Preparations must not be used on animals except under the direct care, authority. or prescription of a veterinarian The veterinarian must act in accordance with any applicable code of practice in force under section 28 of the Act Preparations compounded and used by veterinarians The veterinarian must act in accordance with any applicable code of practice in force under section 28 of the Act Preparations must not be used on animals except under the direct care, authority, or prescription of a veterinarian Substance or biological compound or mix of substances or biological compounds (to which this schedule does not otherwise apply) to be used as a veterinary medicine May be imported only if the Director- General is satisfied that— (a) there is no equivalent veterinary medicine registered under the Act; and (b) it is required to ensure the immediate welfare of animals Must not contain any substance or biological compound that is prohibited for use as an agricultural compound Must not be used on animals except under the direct care, authority, or prescription of a veterinarian The veterinarian must act in accordance with any applicable code of practice in force under section 28 of the Act Topical preparations— Must not be used on the teats of lactating animals if the milk of the animals is and intended for human consumption (a) containing ingredients not able to be absorbed through the skin; (b) used solely to treat minor injuries or to prevent dermatological abnormalities; and Must be manufactured in accordance with good manufacturing practice (c) that do not include any ingredient listed in Schedule 3 Non-medicated anti-diarrhoea preparations Must be manufactured in accordance with good manufacturing practice The label information must include a statement that if the preparation fails to alleviate the condition being treated the user should seek veterinary advice Non-medicated oral laxatives and lubricants Must be manufactured in accordance with good manufacturing practice The label information must include a statement that if the preparation fails to alleviate the condition being treated the user should seek veterinary advice Cauterising preparations used or applied superficially Must be manufactured in accordance with good manufacturing practice The label must include a statement that if the preparation fails to stop bleeding the user should seek veterinary advice Urinary tract modifiers (acidifiers and alkalisers) that are oral preparations used solely for modification of urinary pH Must not be used on animals from which animal material is intended to be used for the production of human food or human pharmaceutical products Must be manufactured in accordance with good manufacturing practice Must be packaged for sale in dosage-size packages (not in bulk or concentrated form) appropriate for the animals for which the agricultural compound is recommended Respiratory tract modifiers (expectorants and cough suppressants) that— Must not be used on animals from which animal material is intended to be used or the production of human food or human pharmaceutical products (a) have only a locally acting, superficial effect on the respiratory tract; and (b) are given orally, applied topically to the nose, or inhaled; and Must be manufactured in accordance with good manufacturing practice (c) are used solely in companion animals to promote mucolysis, cough suppression (by alleviating only irritation) and relieve compromised airways and upper respiratory tract congestion Must be packaged for sale in dosage-size packages (not in bulk or concentrated form) appropriate for the animals for which the agricultural compound is recommended Compounds used to extend animal semen or to be used as media for animal ova An applicable code of practice must be must in force under section 28 of the Act and be complied with Spray markers that are coloured indicators to show where liquid agri-chemicals have been applied to help prevent overlaps Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Plant compound adjuvants, including unless wetting and sticking agents, pH buffers, drift retardants, and water conditioners Must not be used on food crops they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Repellants applied directly to plants and used solely to repel vertebrates or invertebrates Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Attractants applied directly to plants and used solely to attract vertebrates or invertebrates Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Mating disrupters applied directly to plants and used solely to interfere with the reproduction of invertebrates Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Anti-transpirants used solely to prevent drying of plants Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Frost protectants of a chemical nature used solely to prevent frost damage Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment Sunblocks used solely to prevent or reduce sunburn in plants Must not be used on food crops unless they do not produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment
Schedule 3
Ingredients excluded from topical preparations containing ingredients not able to be absorbed through skin and used solely to treat minor injuries or to prevent dermatological abnormalitiesSchedule 2
Ingredient
Antibiotics
Schedule 4
Oral nutritional compounds exempt from registration under sections 21 and 27 of Act if following conditions complied withr 8
1 They must be supplied with a label containing the following information:
(a) trade name:
(b) the name and address of the producer, if applicable:
(c) the name and address of the manufacturer, if applicable:
(d) ingredients:
(e) directions for use, including the species, type, and class of animal intended to be used for:
(f) details of any precautions to be taken to prevent or manage risks described in section 19 of the Act when being used, particularly potential hazards to animals fed with or exposed to them:
(g) batch number, if applicable:
(h) manufacturing date, if applicable:
(i) use by date or expiry date, if applicable.
2 They must be fit for the purpose of feeding to the species, type, and class of animal specified under clause 1(e).
3 They are fit for their purpose only if they are used as recommended and do not do any of the following:
(a) produce residues in primary produce that fail to comply with applicable food residue standards set in or under any enactment:
(b) result in toxic reactions causing pain or distress in the animal:
(c) result in malnutrition causing pain or distress in the animal:
(d) result in physical harm causing pain or distress in the animal:
(e) contain pathogenic micro-organisms at levels that could cause disease resulting in pain and distress in the animal.
4 Agricultural compounds that are therapeutic or pharmacological substances or preparations may be incorporated into oral nutritional compounds only if—
(a) the agricultural compounds are registered under the Act; and
(b) the incorporation of the agricultural compounds is consistent with any conditions of their registration.
5 Feed additives may be used in oral nutritional compounds only if the feed additives are described in Schedule 7 and used in accordance with any relevant limitations specified in that schedule.
6 Oral nutritional compounds that are feed commodities are subject only to clauses 2 and 3. For the purposes of this clause, feed commodities means plants (or any part or parts of those plants) that are raised in an agricultural context and used as feed or for feed production for animals.
Schedule 2 |
Schedule 7
Substances generally recognised as safe if used in accordance with any applicable conditions in Schedule 4Schedule 4
Substances generally regarded as safe feed additives in oral nutritional compounds
Interpretation
A reference to a substance is to all forms of the substance unless a chemical abstract (CAS) number is specified or otherwise stated. Where the first column refers to an organism (including plants), the reference means the whole or any part or any extract of the organism.
General limitations
Each substance in this schedule is subject to the following limitations:
•that it is included in a trade name product formulated in accordance with good manufacturing practice; and
•that it is of an appropriate grade, and the amount added to the product must not exceed the amount reasonably required to accomplish the intended technical effect.
Substance Identification Limitations CAS number (if appropriate) unless otherwise stated Acacia (Gum arabic) 5/01/9000 Acetic acid 64-19-7 Acetophenone 98-86-2 Adipic acid 124-04-9 Aldehyde C-18 104-61-0 Allium sativum Almond shell meal Aloe vera alpha-galactosidase From the following sources: Aspergillus niger, var. Morteirella vinaceae, var. raffinoutiliser. Sacchcaromyces sp. alpha-pinene 80-56-8 When used at no more than 2% by weight of pesticide formulations Aluminium hydroxide 20768-67-6 Ammonium chloride 12125-02-9 Ammonium formate 540-69-2 Ammonium hydroxide 1336-21-6 Ammonium phosphate (mono or dibasic) 7722-76-1 Ammonium propionate Ammonium sulphate 7783-20-2 Amyl butyrate 540-18-1 Amylase From the following sources: Animal pancreatic tissue, Aspergillus oryzae, var. Aspergillus niger, var. Bacillus amyloliquefaciens, B. lentus, B. licheniformis, B. licheniformis containing a B. stearothermophilus gene for alpha-amylase, B. stearothermophilus. B. subtilis containing a B. megatrium gene for alpha-amylase, B. subtilis containing B. stearothermophilus gene for alpha-amylase, B. subtilis, var. Barley malt, Rhizopus niveus, rhizopus oryzae, var. Anethole 4180-23-8 p-Anisaldehyde 123-11-5 Aniseed oil 8007-70-3 Anisole 100-66-3 Apple flavour Ascorbic acid 50-81-7 Ascorbyl palmitate 137-66-6 Aspartame 22839-47-0 Aspergillus niger Aspergillus oryzae Astaxanthin Bacillus licheniformis Bacillus subtilis Non-pathogenic strains Beeswax Beetroot Bentonite 1302-78-9 Benzaldehyde 100-52-7 Benzoic acid 65-85-0 Not more than 0.1% of final feed Benzyl acetate 140-11-4 Benzyl alcohol 100-51-6 beta-apo-8 carotenoic acid ethyl ester 1109-11-1 beta-carotene beta-glucanase From the following sources: Aspergillus niger, var. Bacillus lentius, B. subtilis, var. Humicola insolens, Trichoderma longibrachiatum Betaine hydrochloride 590-46-5 Bifidobacterium spp. Biospernum montanum Birch oil Boerhavia diffusa Brilliant Black BN 2519-30-4 Brilliant Blue FCF 3844-45-9 Bromolain 9001-00-7 Bronopol Butterscotch flavour Butylated hydroxy-anisole 25013-16-5 Total content of antioxidants must be not more than 0.02% fat content of feed Butylated hydroxy-toluene 64742-46-7 Total content of antioxidants must be not more than 0.02% fat content of feed Butyric acid 107-92-6 Calcium carbonate 471-34-1 Calcium caseinate 9005-46-3 Calcium chloride 10035-04-8 Calcium disodium EDTA 662-33-9 Calcium formate 544-17-2 Calcium hydroxide 1305-62-0 Calcium lactate 814-80-2 Calcium lignosulfonate 8061-52-7 Calcium oxide 1305-78-8 Calcium propionate 4057-81-4 Calcium silicate 1344-95-2 Calcium sulphate 7778-18-9 Camphor Maximum of 5% in premixes used in production of animal feeds Candida pintolepesii Canthaxanthin 514-78-3 Capric [decanoic] acid 334-48-5 Caproic acid 142-62-1 Caprylic acid 124-07-2 Capsanthin 465-42-9 Caramel Caraway Carbon black 1333-86-4 Carminic acid 1260-17-9 Carmosine [azorubine] 3567-69-9 Carnauba wax 8015-86-9 Carob 9000-40-2 Carophyll pink 514-78-3 Carrageenan 1/07/9000 i-carrageenan 1/07/9062 k-carrageenan 11114-20-8 1-carrageenan 9064-57-7 Cassia gum 5373-11-5 / 8013-11-4 Cayenne pepper Cedrus deodura Cellulase From the following sources: Aspergillus niger, var. Bacillus lentus, Humicola insolens, Trichoderma longibrachiatum Cellulose 9004-34-6 Charcoal, activated Chlorophyll 1406-65-1 Chocolate brown 4553-89-3 Choline chloride 68-48-1 Chromium proprionates Chymotrypsin Cinnamic aldehyde 104-55-2 Cinnamon Citranaxanthin Citric acid 77-92-9 Clove oil 8000-34-8 Cobalt carbonate 513-79-1 Colour Amaranth 915-67-3 Colour Brown HT 4556-89-3 Colour Green S 3087-16-9 Colour Indigo Carmine Blue 860-22-0 Copper carbonate 1184-64-1 Corn sugar Cryptoxanthin 465-42-9 Curcuma domestics Curcuma longa Cyperus scarriosus Specify source Dandelion Diacetyl 431-03-8 Diatomaceous earth 7631-86-9 Dicalcium phosphate 7789-77-7 2,4-Dichlorobenzyl 1777-82-8 To be used as a preservative alcohol only Didecyl dimethyl ammonium bromide 2390-68-3 Dimethyl polysiloxane 8050-81-5 Disodium EDTA 139-33-3 No more than 240 mg/kg in finished feed Disodium guanylate 9/12/5550 Disodium inosinate 4691-65-0 Dolomite 16389-88-1 Echinacea Elephantopous scaber Embelia ribes Maximum of 5% in premixes used in production of animal feeds Enterococcus faecium Erythorbic acid 7378-23-6 Erythrosine 16423-68-0 Ethoxyquin 91-153-2 Maximum quantity used and to remain in feed must be not more than 0.015% Ethyl acetate 141-78-6 Ethyl alcohol 64-17-5 Not more than 10% of the formulation Ethyl butyrate 105-54-4 Ethyl formate 109-94-4 Ethyl-o-aminobenzoate Ethyl phenylacetate 101-97-3 Ethyl propionate 105-37-3 Ethyl sorbate 2396-84-1 Ethyl vanillin 121-32-4 Ethylene diamine tetra-acetic acid 60-00-4 Fennel 8006-84-6 Fenugreek Ferric chloride 7705-08-0 Ferrous oxide 1345-25-1 Ferrous sulphate 7720-78-7 Food starch and food starch (modified) Use at a level not in excess of the amount reasonably required to accomplish the intended effect Formaldehyde 50-00-0 Not more than 0.25% of final feed Formic acid 64-18-6 Fumaric acid 110-17-8 Garlic 8000-78-0 Ginger 7/08/8007 Glucose Includes dextrose and its hydrated and anhydrous forms Glutamic acid 617-65-2 Glycerides (mono and di) Glycerine 56-81-5 Glycerol 56-81-5 Glycerol mono-oleate 25496-72-4 Glycerol monostearate 31566-31-1 Guar gum 9000-30-0 Gypsum 10101-41-4 / 3397-24-5 Haematococcus algae Hemicellulase From the following sources: Aspergillus niger, var. A. aculeatus, Bacillus lentus, B. subtilis. var. Humicola insolens. Trichoderma longibrachiatum Holarrhena antidys-tenterica 3-Hydroxy-2-methyl-4-pyrone (Palatone/Maltol) 118-71-8 Use at a level not in excess of the amount reasonably required to accomplish the intended effect Hydroxypropyl cellulose 9004-64-2 Inulin 9005-80-5 Iron oxides (black) 1317-61-9 Iron oxides (red) 1309-37-1 Iron oxides (yellow) 5 1 274-00-1 Iso-eugenol 97-54-1 Isopropyl alcohol 67-63-0 Kaolin 1332-58-7 Kon jac gum 9000-36-6 Lactic acid 50-21-5 Lactobacillus acidophilus Lactobacillus bifidus Lactobacillus bulgaricus Lactobacillus casei 68333-14-2 Lactobacillus fermentum Lactobacillus plantarum Lactobacillus rhannosus Lactose 63-42-3 Lauric acid 143-07-7 Lecithin 8002-43-5 Lemon grass Lemon oil 8008-56-8 Licorice (Glycyrrhiza) Includes all licorice derivatives. Not more than 0.1% in final feed Lignosulphonates Lime oil 8008-26-2 Limonene 138-86-3 Linalool 78-70-6 Lipase From the following sources: Animal pancreatic tissue. aspergillus niger, var. A. oryzae, var. Candida rugosa, edible forestomach of calves, kids. and lambs Locust bean gum 9000-40-2 Lutein 57-83-0 Lycopene 502-65-8 Macrogol esters (poly-ethylene esters) 9000-99-3 Magnesium acetate 142-72-3 Includes hydrated forms. Only added to the levels needed Magnesium aluminium silicate 1327-43-1 Includes hydrated forms. Only added to the levels needed Magnesium aspartate 18962-61-3 Includes hydrated forms. Only added to the levels needed Magnesium carbonate 546-93-0 Includes hydrated forms. Only added to the levels needed Magnesium chloride 7791-18-6 Includes hydrated forms. Only added to the levels needed Magnesium citrate 3344-18-1 Includes hydrated forms. Only added to the levels needed Magnesium gluconate 3632-91-5 Includes hydrated forms. Only added to the levels needed Magnesium glutamate 64407-99-4 Includes hydrated forms. Only added to the levels needed Magnesium glycerophosphate 927-20-8 Includes hydrated forms. Only added to the levels needed Magnesium hydroxide 12141-11-6 Includes hydrated forms. Only added to the levels needed Magnesium hypophosphite Includes hydrated forms. Only added to the levels needed Magnesium orotate 34717-03-8 Includes hydrated forms. Only added to the levels needed Magnesium oxide 1309-48-4 Includes hydrated forms. Only added to the levels needed Magnesium phosphate 10043-83-1 Includes hydrated forms. Only added to the levels needed Magnesium silicate 1343 88-0 Includes hydrated forms. Only added to the levels needed Magnesium stearate 557-04-0 Includes hydrated forms. Only added to the levels needed Magnesium sulphate 7487-88-9 Includes hydrated forms. Only added to the levels needed Magnesium trisilicate 14987-04-3 Includes hydrated forms. Only added to the levels needed Malic acid 6915-15-7 Maltodextrin 9050-36-6 Maltol 118-71-8 Mannitol 87-78-5 Marigold (Aztec) Menthol Not for use in cats Methyl alcohol 67-56-1 6-Methyl-5-hepten-2-one 110-93-0 3-Methyl-3-phenyl glycidic acid, ethyl ester 77-83-8 Methyl salicylate 119-36-8 Mineral oil High viscosity Monoisopropyl citrate 1321-57-9 Monopotassium phosphate 7778-77-0 Monosodium glutamate 32221-81-1 Myrica nagi Neohesperidine dihydrochalcone 20702-77-6 When used at no more than 30 ppm in finished feed Neotame 165450-17-9 Nonyl phenol ethoxylate Oatflour Octyl gallate 1034-01-1 Onion oil 2179-59-1 Operculina turpethum Orange oil 8008-57-9 Oregano Pancreatin Papain 9001-73-4 Paprika Parabens, including the following: Benzyl paraben 94-26-8 Calcium methyl paraben 83542-69-2 Calcium propyl paraben 94-18-8 Ethyl paraben 120-47-8 4-Hydroxy benzoic acid 99-96-7 Methyl paraben 99-76-3 Propyl paraben 94-13-3 Sodium butyl paraben 40167-95-1 Sodium methyl paraben 5026-62-0 Sodium propyl paraben 35285-69-9 Para-formaldehyde 30525-89-4 Not more than 0.25% of final feed Patent Blue V 129-17-9 Pectinase 9032-75-1 Pediococcus acidilactici Pediococcus pentosaceus Peppermint oil Not for use in cats Pericol black 2519-30-4 Phosphoric acid 7664-38-2 Phyllanthus emblica Phytase From the following sources: Aspergillus niger, var. A. oryzae, var. Picorhiza kurroa Piper longum Piper nigrum Piper officinarum Pistacia integerima Plumbago zeylanica Polyoxyl 35 castor oil (Cremphor EL) Polyoxyl 40 castor oil (Cremphor RH 40) Polyoxyl 60 castor oil (Cremphor RH 60) Polyoxyethylene nonyl phenol ether 9016-45-9 Only to be used as a wetting agent. Not more than 0.5% of formulated product Polyethylene oxide, polyproylene glycol block copolymer 6/11/9003 Polyoxyethylene (20) sorbitan monooleate 9005-65-6 Polyvinylpyrrolidone 9003-39-8 Ponceau 4R 2611-82-7 When used at no more than 50 mg/kg in finished feed Potassium carbonate 584-08-7 Potassium chloride 7447-40-7 Potassium hydroxide 1310-58-3 Potassium lactate 996-31-6 Potassium/sodium lactate mixture Potassium sorbate 590-00-1 Propionic acid 79-09-4 Propyl acetate 109-60-4 Propyl alcohol 71-23-8 Not more than 55 g/head/day Propyl benzoate 2315-68-6 Propyl gallate 121-79-9 Total content of antioxidants must be not more than 0.02% fat content of feed Propylene glycol 57-55-6 Protease From the following sources: Aspergillus niger, var. A. oryzae. var. Bacillus amyloliquefaciens, B. licheniformis. B. subtilis, var. B. subtilis, containing a B. amyloliquefaciens gene for protease Pumice Raffinase Rapeseed oil 8002-13-9 Raspberry flavour Rennet Rosemary 8000-25-7 Rum ether 8030-89-5 Rutin 153-18-4 Saccharin sodium 128-44-9 Saccharomyces cerevisiae Sage oil Silica (silicon dioxide) 7631-86-9 Silicone antifoam 63148-62-9 Skatole 83-34-1 Smokey bacon flavour Sodium acid pyrophosphate Sodium alginate 9005-38-3 Sodium alkyl benzene sulphonate 25155-30-0 Sodium aluminosilicate 73987-94-7 Sodium ascorbate 134-03-2 Sodium benzoate 532-32-1 Not more than 0.1% of final feed Sodium bicarbonate 144-55-8 Sodium carbonate 497-19-8 Sodium carboxy methylcellulose 9004-32-4 Sodium chloride 7647-14-5 Sodium citrate 68-04-2 Sodium cyclamate 139-05-9 Sodium erythorbate 6381-77-7 Sodium formate 141-53-7 Sodium hex-ametaphosphate 10124-56-8 Sodium hydroxide 1310-73-2 Sodium lignosulphonate 8061-51-6 Sodium metabisulphite 7681-57-4 Sodium nitrite 7632-00-0 Not more than 1% of final feed Sodium propionate 137-40-6 Sodium silico aluminate 1344-00-9 Not more than 2% of final feed Sodium tri-polyphosphate 7758-29-4 Sorbic acid 110-44-l Sorbitan monostearate 1338-41-6 Sorbitol 50-70-4 Strawberry flavour Streptococcus (Enterococcus) salivarius subspecies thermophilus Sulphamic acid 5329-14-6 Sulphuric acid 7664-93-9 Sunflower oil 8001-21-6 Sunset yellow 2783-94-0 Tagetes oil 8016-84-0 Tangerine oil 8008-31-9 Tartaric acid 87-69-4 Tartrazine 1934-21-0 Terminalia balerica Terminalia chebula Tertiary butylhydroqui none (TBHQ) 1984-33-0 Tetra potassium pyro-phosphate 7758-87-4 Tetra sodium pyrophosphate 7722-88-5 Thaumatin 53850-34-3 Thyme oil 8007-46-3 Thymol 89-83-8 When added at levels consistent with good feeding practice Titanium dioxide 13463-67-7 Tocopherols (extracts of natural origin) 1406-66-2 Tricalcium phosphate 7758-87-4 Trimethylamine 75-50-3 Trypsin Turmeric 8024-37-1 Undecylenic alcohol 112-43-6 Valerian Valeric acid 109-52-4 Vanillin 121-33-5 Vermiculite 1318-00-9 Vitamin B1 Vitamin B12 Xanthan gum 11138-66-2 Xanthophyll 127-40-2 Xylanase From Aspergillus oryzae carrying a gene from Thermomyces lanuginosus coding for xylanase Yucca schidigera Zeaxanthin Zinc oxide 1314-13-2 Zinc proprionates Zingiber officinale
Diane Morcom,
Clerk of the Executive Council.
Explanatory note
This note is not part of the regulations, but is intended to indicate their general effect.
These regulations, which come into force on the 28th day after their notification in the Gazette, amend the Agricultural Compounds and Veterinary Medicines Regulations 2001 ( “the principal regulations”
).
The amendment—
-
•inserts new regulation 5A into the principal regulations, which provides that a combined agricultural compound—
•is exempt from registration under section 21 or 27 of the Agricultural Compounds and Veterinary Medicines Act 1997 (the Act) if the agricultural compound is a combination of 2 or more agricultural compounds that are exempt from registration under these regulations:
-
•is subject to any—
•prescribed conditions; and
•other provision of these regulations that applies to each agricultural compound that comprises the combined agricultural compound:
•revokes regulation 7 of the principal regulations (which relates to reports on agricultural compounds):
-
•substitutes the following schedules:
•Schedule 1 (which lists agricultural compounds that are exempt from registration if applicable codes of practice are complied with) has been amended to insert 3 new compounds into, and to exclude 5 compounds from, item 1 of the former Schedule 1:
-
•Schedule 2 (which lists agricultural compounds that are exempt from registration if certain conditions are complied with) has been amended to include the compounds listed in the former Schedule 3 of the principal regulations, and to insert—
•a new condition in relation to oral and topical preparations:
•a new compound into the schedule, namely, any compound that is used to extend animal semen or to be used as media for animal ova:
•New Schedule 3 (which lists excluded ingredients for topical preparations):
•Schedule 4 (which lists conditions that apply to oral nutritional compounds exempt from registration) has been amended to include a new criteria for determining whether an oral nutritional compound is fit for its purpose, namely, that its use does not result in physical harm causing pain or distress in an animal:
•Schedule 7 (which lists substances that are generally recognised as safe feed additives in oral nutritional compounds) has been amended by removing Part B and inserting new items into the schedule.
Issued under the authority of the Acts and Regulations Publication Act 1989.
Date of notification in Gazette: 14 April 2005.
Contents
1General
2About this eprint
3List of amendments incorporated in this eprint (most recent first)
Notes
1 General
-
This is an eprint of the Agricultural Compounds and Veterinary Medicines Amendment Regulations 2005. The eprint incorporates all the amendments to the regulations as at 1 November 2011. The list of amendments at the end of these notes specifies all the amendments incorporated into this eprint since 3 September 2007.
Relevant provisions of any amending enactments that contain transitional, savings, or application provisions that cannot be compiled in the eprint are also included, after the principal enactment, in chronological order.
2 About this eprint
This eprint has not been officialised. For more information about eprints and officialisation, please see http://www.pco.parliament.govt.nz/eprints/
.
3 List of amendments incorporated in this eprint (most recent first)
Agricultural Compounds and Veterinary Medicines (Exemptions and Prohibited Substances) Regulations 2011 (SR 2011/327): regulation 16
1 SR 2001/101