NOBILIS FOWL POX VACCINE

Ország: Ausztrália

Nyelv: angol

Forrás: APVMA (Australian Pesticides and Veterinary Medicines Authority)

Aktív összetevők:

FOWL POX VACCINE

Beszerezhető a:

INTERVET AUSTRALIA PTY LIMITED

INN (nemzetközi neve):

vaccine - fowl pox

Gyógyszerészeti forma:

MISC. VACCINES OR ANTI SERA

Összetétel:

FOWL POX VACCINE VACCINE-VIRAL Active 0.0 P

db csomag:

1-25 vials; 50x1000; 50x2000; dose vials

Osztály:

VM - Veterinary Medicine

Gyártó:

INTERVET AUSTRALIA

Terápiás csoport:

POULTRY | TURKEYS | BREEDER | BREEDERS | BROILER | BROILER BREEDER | CHICKENS | CHICKS | CHOOKS | DAY OLD CHICKS | HATCHLINGS |

Terápiás terület:

IMMUNOTHERAPY

Terápiás javallatok:

FOWL POX

Termék összefoglaló:

Poison schedule: 0; Host/pest details: POULTRY: [FOWL POX]; TURKEYS: [FOWL POX]; Poison schedule: 0; Withholding period: WHP: Meat: Nil. Eggs: Nil.; Host/pest details: POULTRY: [FOWL POX]; TURKEYS: [FOWL POX]; Poison schedule: 0; Withholding period: ; Host/pest details: POULTRY: [FOWL POX]; TURKEYS: [FOWL POX]; For use in the prevention of fowl pox disease in chickens and turkeys.

Engedélyezési státusz:

Registered

Engedély dátuma:

2023-07-01

Betegtájékoztató

TEMPLATE FOR RELEVANT LABEL PARTICULARS (RLPS) _(VETERINARY PRODUCTS)
_
_ _
APVMA NO:
40542
DATE: 31
ST OCTOBER 2012_ _
PRODUCT NAME:
NOBILIS
® FOWL POX VACCINE
_Select appropriate: _

New Product (include all applicable RLPs) OR

Variation (highlight instructions that are being varied). Approval no.
of label being
varied: 40542/52732
Label Components include in product label: Vial and Carton
LABEL PARTICULAR
TEXT
LABEL COMPONENTS
Signal heading:
FOR ANIMAL TREATMENT ONLY
Vial, Carton front and inner lid
panel
Product name:
NOBILIS
® FOWL POX VACCINE
Vial, Carton front and inner lid
panel
Active constituent/s:
VIAL: Fowl Pox virus (living, attenuated)
CARTON FRONT AND INNER LID PANEL: Active Constituent:
Fowl Pox Virus, living, attenuated (Ref: B/203).
Minimum titre at end of shelf life 10
3.0
TCID
50
/ per dose.
As specified.
Statement of claims:
For use in the prevention of Fowl Pox disease in chickens and turkeys.
Carton front and inner lid panel
Net contents:
VIAL: Doses per vial – Refer to pack
CARTON: Contents: 1 to 25, 50 vials x 1000 or 2000 dose vials

No. of vials
As specified.
Directions for Use
Heading:
Vial: READ INFORMATION INSIDE PACK BEFORE USE.
Carton Front Panel: READ THE INFORMATION PRINTED ON THE INSIDE OF
THE PACK BEFORE USING THIS PRODUCT.
As specified. RLP APPROVED
LABEL PARTICULAR
TEXT
LABEL COMPONENTS
Carton Inner Lid Panel: DIRECTIONS FOR USE:
Restraints:
Not required.
Contraindications:
Not required.
Precautions:
PRECAUTIONS:
Administer to birds from day-old. Avoid damage to vaccinated stock.
Sterilise all
injection equipment by boiling before use. Avoid the use of strong
disinfectants for
sterilisation. Maintain cleanliness at all times. Keep vaccinators**
sharp and clean.
Replace as required. Avoid inoculation of wet or heavily soiled
animals. This
product must be inoculated only by wing web stab.
Side effects:
Not required.
Dosage &
administration:
DOSAGE AND ADMINISTRATION:
1) Each vaccine vial contains a dry pellet of lyophillised vaccine
equivalent to the
dose indicat

Termékjellemzők

PRODUCT NAME: NOBILIS FOWL POX VACCINE
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: [phone] (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 FOWL POX VACCINE, FOWL POX VACCINE #2
PRODUCT CODE:
3961,
RECOMMENDED USE:
To protect poultry against Fowl Pox.
APVMA NO:
40542, 60345
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 2.5mL 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.
POTENTIAL HEALTH EFFECTS
EMERGENCY OVERVIEW
SECTION 2 - HAZARDS IDENTIFICATION
SECTION 1 - IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY
ISSUED BY: INTERVET AUSTRALIA PTY LIMITED
(TRADING AS MSD ANIMAL HEALTH)
91-105 HARPIN STREET
TEL: [phone] (BUSINESS HOURS)
BENDIGO EAST, VIC 3550, AUSTRALIA
FAX: [phone]
COMPANY ABN: 79 008 467 034
PRODUCT NAME: NOBILIS FOWL POX V