Negara: Australia
Bahasa: Inggris
Sumber: APVMA (Australian Pesticides and Veterinary Medicines Authority)
COPPER AS COPPER GLYCINATE
TROY LABORATORIES PTY LTD
Cu as copper glycinate(60mg/mL)
PARENTERAL LIQUID/SOLUTION/SUSPENSION
COPPER AS COPPER GLYCINATE MINERAL-COPPER Active 60.0 mg/ml
100mL; 250mL
VM - Veterinary Medicine
TROY LABORATORIES
CALF | CATTLE | BEEF | BEEF CALF | BOS INDICUS | BOS TAURUS | BOVINE | BUFFALO | BULL | BULLOCK | CALF | CALF - PODDY | CALF - P
NUTRITION & METABOLISM
COPPER DEFICIENCY
Poison schedule: 6; Withholding period: WHP: MEAT: NIL MILK: NIL ESI: Zero ( 0) days; Host/pest details: CALF: [COPPER DEFICIENCY]; CATTLE: [COPPER DEFICIENCY]; Poison schedule: 6; Withholding period: ; Host/pest details: CALF: [COPPER DEFICIENCY]; CATTLE: [COPPER DEFICIENCY]; For the prevention and treatment of copper deficiency in cattle.Excessive copper is toxic; do not administer unless copper deficiency has been confirmed
Registered
2023-07-01
19 OCT 2010 TROY COPPERNATE INJECTION PRIMARY LABEL DRAFT: Front Panel: POISON KEEP OUT OF REACH OF CH ILDREN READ SAFETY DIRECTIONS BEFORE OPENING OR USING FOR ANIMAL TREATMENT ONLY Ancillary Panels: TROY COPPERNATE INJECTION ACTIVE CONSTITUENT: 60 mg/ml COPPER as COPPER GLYCINATE FOR THE PREVENTI ON AND TREATMENT OF COPPER DEFICIENCY IN .CATTLE 100mL, 250mL READ THE ATTACH ED LEAFLET BEFORE USING: DIRECTIONS FOR USE: • RLP Appr oved Use contents w ith in 24 hours of first broaching of the vi al. Discard the· unused portion. Excess iv e copper is toxic; do not adm inis ter unle ss copper deficiency has been confirmed . Swelling may occur at injection site whi ch usually recedes in a few weeks. Anaphylactic reactions following admi ni strat ion may occur in young bovines. Prompt an tihistamine treatment is indicated. · SHAKE WELL BEFORE USE CATTLE: 2 ml, S.C., repeated within 6-9 months CALV ES : 1 ml, S.C., repeated within 3-6 mon th s WITHHOLDING PERIODS: MEAT: NIL MILK: NIL TRADE ADVICE: EXPORT SLA UGHTER INTERV AL ( ES I): ze ro (0) days. SAFETY DIRECTIONS May irritate the eyes a nd skin. Avoid contact with eyes and skin. Wash hands after use. Version: V02 Page 1 of 2 Info PEST Verified 19 OCT 2010 TROY COPPERNATE INJECTION PRJMARY LABEL FIRST AID If poisoning occurs, contact a doctor or Poisons Informati on Centre. PHONE AUSTRALIA 131126 TROY LABORATORIES PTY. LTD 31 -35 Glendenning Road, Glendenning NSW 2761 AUSTRALIA W: www.troylab.com. au E: info@troylab.com.au DISPOSE of empty container by wrapping with paper and putting in the garbage. STORE below 25°C (Air Conditioning). APVMA Approval No.: 50441/50148 Batch: Expi ry: CDXXXX Version: V02 Page 2 of2 ,. 19 OCT 2010 TROY COPPERNATE INJECTION IMMEDIATE LABEL DRAFT: Front Panel: POISON KEEP OUT OF REACH OF CHILDREN READ SAFETY DIRECTIONS BEFORE OPENING OR USING FOR ANIMAL TREATMENT ONLY Ancillary Panels: TROY COPPERNATE INJECTION ACTIVE CONSTITUENT: 60 mg/ml COPPER as COPPER GL YCINATE FOR THE PREVENTION AND TREATMENT OF COPPER DEFICIENCY IN CATTLE 1 Baca dokumen lengkapnya
MATERIAL SAFETY DATA SHEET PRODUCT NAME: TROY COPPERNATE INJECTION PAGE: 1 OF 4 THIS REVISION ISSUED: JULY, 2010 MATERIAL SAFETY DATA SHEET Issued by: Troy Laboratories Australia Pty Ltd Phone: 02 9677 9000 POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA, (0800 764 766 IN NEW ZEALAND) SECTION 1 - IDENTIFICATION OF THE MATERIAL AND SUPPLIER TROY LABORATORIES AUSTRALIA PTY. LTD ABN: 21 000 283 769 TEL: (02)9677 9000 31-35 GLENDENNING ROAD FAX: (02) 9677 9300 GLENDENNING NSW 2761 CHEMICAL NATURE: Water suspension of copper complex. TRADE NAME: TROY COPPERNATE INJECTION PRODUCT CODE: 50441 PRODUCT USE: Prevention and treatment of copper deficiency in cattle. CREATION DATE: JULY, 2005 THIS VERSION ISSUED: JULY, 2010 and is valid for 5 years from this date. SECTION 2 - HAZARDS IDENTIFICATION STATEMENT OF HAZARDOUS NATURE This product is classified as: Not classified as hazardous according to the criteria of SWA Australia. Not a Dangerous Good according to the Australian Dangerous Goods (ADG) Code. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: Not Hazardous - No criteria found. SUSDP CLASSIFICATION: S6 ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated EMERGENCY OVERVIEW PHYSICAL DESCRIPTION & COLOUR : Purplish-blue to dark blue micronised suspension. ODOUR: Mild odour. MAJOR HEALTH HAZARDS: no significant risk factors have been found for this product. POTENTIAL HEALTH EFFECTS INHALATION SHORT TERM EXPOSURE: Significant inhalation exposure is considered to be unlikely. Available data indicates that this product is not harmful. In addition product is unlikely to cause any discomfort or irritation. LONG TERM EXPOSURE: No data for health effects associated with long term inhalation. SKIN CONTACT: SHORT TERM EXPOSURE: Available data indicates that this product is not harmful. It should present no hazards in normal use. However product may be mildly irritating, but is unlikely to cause anything more than mild discomfort which should disappe Baca dokumen lengkapnya