מדינה: אוסטרליה
שפה: אנגלית
מקור: APVMA (Australian Pesticides and Veterinary Medicines Authority)
LIVE FOWL ADENOVIRUS
INTERVET AUSTRALIA PTY LIMITED
vaccine - fowl adenovirus
MISC. VACCINES OR ANTI SERA
LIVE FOWL ADENOVIRUS VACCINE-VIRAL Active 0.0 ml
#50x2000; #Dose/Vial; *50x1000; *Dose/Vial; 1-25 vials
VM - Veterinary Medicine
INTERVET AUSTRALIA
POULTRY CHICKS - UP TO 28 DAYS OLD | CHICKS OF VACCINATED HENS
IMMUNOTHERAPY
HOMOLOGOUS TYPES OF FOWL ADENOVIRUS INFE | INCLUSION BODY HEPATITUS
Poison schedule: 0; Withholding period: WHP: Nil.; Host/pest details: POULTRY CHICKS - UP TO 28 DAYS OLD: [HOMOLOGOUS TYPES OF FOWL ADENOVIRUS INFE]; Poison schedule: 0; Withholding period: ; Host/pest details: POULTRY CHICKS - UP TO 28 DAYS OLD: [HOMOLOGOUS TYPES OF FOWL ADENOVIRUS INFE]; For the protection of chickens of vaccinated hens against homologous types of fowl adenovirus infection (inclusion body hepatitis) up to 28 days of age.Do not use for poultry in lay or that are in contact with birds in lay for which the serological status to FAV is either unknown or negative. DO NOT USE in laying birds where eggs or egg protein are to be used for human consumption or processing.
Registered
2023-07-01
For Official Use Only E-LABEL APPLICATION (DRAFT) COMPANY NAME: INTERVET AUSTRALIA PTY LIMITED PRODUCT NAME: NOBILIS FAV VACCINE ELABEL APPLICATION NO: DC12-01835671E42 APVMA APPROVAL NO: 52390/100353 PRODUCT NO: 52390 VERSION NO: 6.0 APPLICATION STARTED: 2014-Sep-03 15:34:16 VERSION CREATED: 2015-Jan-07 11:34:06 STARTED BY: Lyn Lavidis PRINTED: 2015-Jan-07 11:46:16 LABEL NAME: NOBILIS FAV VACCINE SIGNAL HEADINGS: FOR ANIMAL TREATMENT ONLY CONSTITUENT STATEMENTS: [Vial] Fowl Adenovirus, living (Esurient strain) [Pack insert front and back] ACTIVE CONSTITUENT: Fowl Adenovirus, living (Esurient strain) 10^6.1 TCID50 per mL CLAIMS: For the protection of chickens of vaccinated hens against homologous types of fowl adenovirus infection (inclusion body hepatitis) up to 28 days of age. NET CONTENTS: [Vial] Doses per vial – Refer to pack [Pack Insert Front] Contents: 1-25 [50] vials [Tamperproof label] Doses: 1000[2000] / vial DIRECTIONS FOR USE: READ PACK INSERT BEFORE USE- "Vial" READ THE REVERSE SIDE OF THE PACK INSERT BEFORE USING THE PRODUCT - "Pack Insert front" RESTRAINTS: Do not use for poultry in lay or that are in contact with birds in lay for which the serological status to FAV is either unknown or negative. PRECAUTIONS: [Pack Insert back] Precautions: 1) Intervet Nobilis® FAV Vaccine should be administered to replacement breeder stock before they come into contact with flocks-in-lay for which the FAV antibody status is unknown or negative. If the vaccine were to spread from the flock undergoing vaccination RLP APPROVED For Official Use Only to flocks in lay that are not already antibody-positive to FAV, a disease associated with FAV could occur in the progeny of antibody-negative layers as they become infected and before they develop immunity to FAV. 2) The product must be used immediately upon reconstitution and unused vaccine must be discarded after 2 hours. DOSAGE AND ADMINISTRATION: [Pack Insert back] DOSAGE AND ADMINISTRATION Use entire contents within 2 hours of reconstitution. Vaccination is recomme קרא את המסמך השלם
PRODUCT NAME: NOBILIS MATERIAL SAFETY DATA SHEET THIS REVISION ISSUED: JULY, 2014 PAGE: 1 OF 6 MATERIAL 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) SUBSTANCE: Freeze-dried, live virus. TRADE NAME: NOBILIS FAV VACCINE PRODUCT CODE: 3964 RECOMMENDED USE: For the protection of chickens of vaccinated hens against homologous types of Fowl Adenovirus (FAV) infection (inclusion body hepatitis) up to 28 days of age. APVMA NO: 52390 THIS VERSION ISSUED: Is valid for 5 years from this date. 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 the Australian Dangerous Goods (ADG) Code. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: S22, S25. Do not breathe dust. Avoid contact with eyes. SUSDP CLASSIFICATION: None allocated. ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated PHYSICAL DESCRIPTION & COLOUR: The vaccine is a freeze-dried, live virus vaccine, presented in 9mL antibiotic vials that have been sealed under vacuum and in which there is a 4mL plug of dried vaccine. ODOUR: No distinctive odour. MAJOR HEALTH HAZARDS: no significant risk factors have been found for this product. INHALATION: SHORT TERM EXPOSURE: Available data indicates that this product is not harmful. However product may be mildly irritating, although unlikely to cause anything more than mild transient discomfort. LONG TERM EXPOSURE: No data for health effects associated with long term inhalation. SECTION 1 - IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY SECTION 2 - HAZARDS IDENTIFICATION EMERGENCY OVERVIEW POTENTIAL HEALTH EFFECTS ISSUED BY: INTERVET AUSTRALIA PTY LIMITED (TRADING AS MSD ANIMAL HEALTH) 91-105 HARPIN STREET TEL: 1 800 033 461 (BUSINESS HOURS) BENDIGO EAST, VIC 3550, AUSTRALIA FAX: 1 800 קרא את המסמך השלם