Nchi: Australia
Lugha: Kiingereza
Chanzo: APVMA (Australian Pesticides and Veterinary Medicines Authority)
CONCENTRATED ANTIGENS OF DICHELOBACTER NODOSUS; LIGHT LIQUID PARAFFIN; THIOMERSAL
INTERVET AUSTRALIA PTY LIMITED
Dichelobacter nodosus(100ug/mL)
MISC. VACCINES OR ANTI SERA
CONCENTRATED ANTIGENS OF DICHELOBACTER NODOSUS VACCINE-ANTIGEN/ANTIBODY Active 100.0 ug/ml; LIGHT LIQUID PARAFFIN UNGROUPED Other 600.0 ul/ml; THIOMERSAL MERCURY Other 0.05 mg/ml
100mL; 1L; 250mL; 500mL; 50mL
VM - Veterinary Medicine
INTERVET AUSTRALIA
LAMB | SHEEP | EWE | HOGGET | LAMB | OVINE | RAM | WEANER | WETHER
IMMUNOTHERAPY
FOOTROT - DICHELOBACTER NODOSUS
Poison schedule: 0; Withholding period: WHP: Nil. Trade Advice: Export Slaught er Interval: ESI: Not Required.; Host/pest details: LAMB: [FOOTROT - DICHELOBACTER NODOSUS]; SHEEP: [FOOTROT - DICHELOBACTER NODOSUS]; Poison schedule: 0; Withholding period: ; Host/pest details: LAMB: [FOOTROT - DICHELOBACTER NODOSUS]; SHEEP: [FOOTROT - DICHELOBACTER NODOSUS]; An aid in the control of footrot in sheep and lambs.
Registered
2023-07-01
U, pre-press art prepared by PROD U CT : SIZE : DIMENSIONS: COLOURS : 1 7/3/08 FOOTVX 1 DDmL CARTO N 162 x 50 x 91 mm PMS123 • PM S293 • BLACK • PMS C YAN AP V MA APPROVAL:51170 /1 DDmU1 007 ITEM N UMBER: 10019 CCP No : 06 / 019A JOB BAG No : J/ 03 1 6-1A TYPE SIZE CHEC K U ST LOGO : 15.2mm KORC / SAFID DIRECTIONS : 2.3mm READ ENCLOSED LEAFLET : 2. Dmm SMALLEST REGULATORY TEXT : 1. 5mm 1J JJ 0 0 i1 m 0 @ (j) co ~ 0 0 i1 )> ~ c )> r (J) N m ~ I m z 1J JJ z -1 m 0 0 z )> .j:>. ....... -·- - ·- --- - - ·- · -·-------- - ·- - ·-· -- - - ·- - ·- _\ -'-;-- R EA D T HE E NCLO SED L EA FLET BEFO RE U SI NG THI S PR OD UCT. DIMCTlQKS FDR USE 1. AYtNlbc!IMVM 1ft tc"'SouiJIWIIel. VIN!tt, Q-uW4, Wt.Ura"'MMIa Nll'bllllanll•lr· 2. VlcduUelllllllt penallleclll 10101 dlttr'ct&tf H..-S.UU.waiu\llttlllut ••PPtMI frM till OtpiMIItrl IIAo1cultu~ttrRI.uai~PftltKtiMielrd a. c.u.ctjCIIItiKIIAunll.llldiPitllctllftloanlfotdttalla. ........... 'lllt 11CdM b lllii"J' tl UIIM I llfp lou! ,.IC\Iell (absclu) It tftl ~ If 'fl0d111UN Ill I slp lf) CII( pnpol'l.llll I I &IN.,_ Wb l lt tlb .. alp wll bt If &llcWt duii!Jollln molllrllbiiCII, I ptn'UIIIIIt IIMmllb .UI f'NIIIIn 111 10111 1 lll lm l lt.Al!Kt Utlllt p,altleallalfrMUO II llle Ill tllll11 1td Drlllsll tMMdLi t b MOCMIIMidld Ullttambt 11 Cidlllttd l ll mt 4- IWM klbelnltl•lftt.NurllftCWIIlll!lll1btco•lllfldldlftetNIZZltn' posallllfWICIId-.ccJUUoadls(Uicluta ) Uitdatll!l:lble, l lldtbll sbllllldbtMidld.WIInla]tcllcl _CllnHU't _ IIIIP 011 tAt &ldt ol' tat ..0 blallll Llll -~tiM,. .aMIIII be mu. DliiiHd tl' IUIIII Madlat: JIOSilbfrlfi!ICl.ld-.cclllallta&ka. A_. I&I IDI IIIHIIIl&II. 2 .JMOIUilprllf t. Uillf .... UUIINIII'1 1111 iKIIIM&IDHlcbl ll llaWMl VKdutlllllllfUIIn lol .. atl& s ol' sl aul)ttr.., MWitll MIO~tllllc I ns weda!.td lltUI wcau tl1aiiii11C. SlullllCDIIltll tl btlmllM- DN : ShHP and IAmbs: lmlii'S U 8CUWf£0US IKJ[Ct\ON. wmtHOUHN QP WO O IUL I'IWl EAtM CE: CXPOAISL.AliCHT{R I NlERYAL(ts i ):CSII'IOtlf! (! ult l!d . U wr Saltty aed nnt .ud lalana.U.a Soma hati kamili
COOPERS OVILIS FOOTVAX SHEEP AND LAMB FOOTROT VACCINE 51170/120552 Product Name: APVMA Approval No: Label Name: COOPERS OVILIS FOOTVAX SHEEP AND LAMB FOOTROT VACCINE Signal Headings: FOR ANIMAL TREATMENT ONLY Constituent Statements: 100 μg/mL of concentrated antigens of: Potency Units Dichelobacter nodosus Serotype A ≥ 1:400 Dichelobacter nodosus Serotype B1 ≥ 1:400 Dichelobacter nodosus Serotype B2 ≥ 1:400 Dichelobacter nodosus Serotype C ≥ 1:400 Dichelobacter nodosus Serotype D ≥ 1:400 Dichelobacter nodosus Serotype E ≥ 1:400 Dichelobacter nodosus Serotype F ≥ 1:400 Dichelobacter nodosus Serotype G ≥ 1:400 Dichelobacter nodosus Serotype H ≥ 1:400 Dichelobacter nodosus Serotype I ≥ 1:400 Contains 0.05 mg/mL thiomersal as preservative. Claims: An aid in the control of footrot in sheep and lambs. Net Contents: 50 mL 100 mL 250 mL 500 mL 1 L Directions for Use: Restraints: Contraindications: Precautions: RLP APPROVED Side Effects: The vaccine may cause a large local swelling at the site of vaccination in a significant proportion of sheep. While this swelling will be of short duration in most instances, occasionally they lead to the formation of abscesses which can burst and discharge. A permanent blemish may remain in some animals. Injection site reactions can be particularly noticeable in rams and British breeds. It is recommended that rams be vaccinated at least 4-6 weeks before joining. All sheep should be vaccinated high on the side of the neck behind the ear – this is particularly important for ewes with lambs at foot, to ensure there is little likelihood of lambs nuzzling potentially infected vaccination sites. Dosage and Administration: Shake well before use. Use of this vaccine may be restricted in your State or Territory. Contact your local Department of Agriculture (or similar) for details. DOSE: Sheep and Lambs – 1mL by SUBCUTANEOUS INJECTION. VACCINATION PROGRAMMES: All sheep in the flock require two doses of FOOTVAX at least six weeks apart for maximum effectiveness. FOOTVAX ca Soma hati kamili
PRODUCT NAME: COOPERS FOOTVAX SHEEP AND LAMB FOOTROT VACCINE SAFETY DATA SHEET THIS REVISION ISSUED: NOVEMBER, 2016 PAGE: 1 OF 6 SAFETY DATA SHEET Issued by: Intervet Australia Pty Limited (trading as MSD Animal Health) Phone: 1 800 033 461 (Business Hours) Poisons Information Centre: 13 11 26 from anywhere in Australia, (0800 764 766 in New Zealand) CHEMICAL NATURE: Water suspension of killed bacteria plus minor ingredients. TRADE NAME: COOPERS FOOTVAX SHEEP AND LAMB FOOTROT VACCINE RECOMMENDED USE: Animal vaccine for use as described on the product label. APVMA NO: 49668 CREATION DATE: July, 2009 THIS VERSION ISSUED: November, 2016 and is valid for 5 years from this date. POISONS INFORMATION CENTRE: PHONE 13 1126 FROM ANYWHERE IN AUSTRALIA STATEMENT OF HAZARDOUS NATURE: THIS PRODUCT IS CLASSIFIED AS: Not classified as hazardous according to the criteria of SWA. Not a Dangerous Good according to Australian Dangerous Goods (ADG) Code, IATA and IMDG/IMSBC criteria. SUSMP CLASSIFICATION: None allocated. ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated GHS SIGNAL WORD: NONE. NOT HAZARDOUS. PREVENTION P102: Keep out of reach of children. P262: Do not get in eyes, on skin, or on clothing. P281: Use personal protective equipment as required. RESPONSE P337: If eye irritation persists: seek medical attention. P352: Wash with plenty of soap and water. P301+P330+P331: IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P370+P378: Not combustible. Use extinguishing media suited to burning materials. STORAGE P402+P404: Store in a dry place. Store in a closed container. P403+P235: Store in a well-ventilated place. Keep cool. DISPOSAL P501: Dispose of contents and containers as specified on the registered label. PHYSICAL DESCRIPTION & COLOUR: A white water-in-oil emulsion vaccine. ODOUR: No data. MAJOR HEALTH HAZARDS: no significant risk factors have been found for this product. EMERGENCY OVERVIEW ISSUED BY: INTERVET AUSTRALIA PTY LIMITED (TRADING AS MSD ANIMAL HEALTH) 91-10 Soma hati kamili