Country: Australia
Language: English
Source: APVMA (Australian Pesticides and Veterinary Medicines Authority)
BOVINE EPHEMERAL FEVER VIRUS (BEFV)
ZOETIS AUSTRALIA PTY LTD
bovine ephemeral fever virus
PARENTERAL LIQUID/SOLUTION/SUSPENSION
BOVINE EPHEMERAL FEVER VIRUS (BEFV) VACCINE-VIRAL Active 0.0 P
#10x20mL; #Diluent; #vials; 1 x 10 dose vaccine; 1 x 20 mL diluent; 10x10 D.V.; Dose = 2mL
VM - Veterinary Medicine
ZOETIS AUSTRALIA
CATTLE | BEEF | BOS INDICUS | BOS TAURUS | BOVINE | BUFFALO | BULL | BULLOCK | CALF | COW | DAIRY COW | HEIFER | STEER
IMMUNOTHERAPY
BOVINE EPHEMERAL FEVER (BEF) | VACCINE | EQUINE ROTAVIRUS | THREE DAY SICKNESS
Poison schedule: 3; Withholding period: WHP: Zero (0) days ESI: Zero (0) days; Host/pest details: CATTLE: [BOVINE EPHEMERAL FEVER (BEF), VACCINE]; Poison schedule: 4; Withholding period: WHP: Nil; Host/pest details: CATTLE: [BOVINE EPHEMERAL FEVER (BEF), VACCINE]; Poison schedule: 4; Withholding period: ; Host/pest details: CATTLE: [BOVINE EPHEMERAL FEVER (BEF), VACCINE]; For the prevention of bovine ephemeral fever (3 day sickness) in cattle.
Registered
2023-07-01
Product Name: APVMA Approval No: ULTRAVAC BEF VACCINE 41461/131429 Label Name: ULTRAVAC BEF VACCINE Signal Headings: FOR ANIMAL TREATMENT ONLY Constituent Statements: Bovine Ephemeral Fever Standard Strain (BB2271-919) at ≥ 10^4.3TCID50/ 2 mL dose Claims: For the prevention of Bovine Ephemeral Fever (3 day sickness) in cattle Net Contents: 10 x 10 doses vaccine 10 x 20 mL diluent 1 x 10 dose vaccine 1 x 20 mL diluent Directions for Use: Restraints: Contraindications: Precautions: Side Effects: Following vaccination with this product, a transient febrile response in animals may be observed. This response could contribute to a sudden drop in milk production by affected dairy cattle. Dosage and Administration: USE ALL RECONSTITUTED PRODUCT IMMEDIATELY. 2 mL dose by subcutaneous injection. Primary vaccination: Cattle require an initial 2 mL dose subcutaneously. The second 2 mL subcutaneous dose can be effectively administered any time from 2 weeks up to 6 months later. Cattle can be vaccinated from 6 months of age. Two doses of vaccine are required to produce long lasting immunity. RLP APPROVED Booster vaccination: 2 mL annual booster dose is required for all cattle. Preparation of the vaccine: 1. Draw up 2 mL of Ultravac BEF Diluent into a sterile syringe. 2. Add to the freeze dried vaccine in the small vial. 3. Draw up reconstituted vaccine into the syringe. 4. Transfer reconstituted vaccine into the Ultravac BEF Diluent bottle. 5. Gently shake the diluent bottle to evenly distribute the vaccine (excessive shaking will cause foaming). 6. Reconstituted vaccine is orange in colour and must be used as soon as possible. General Directions: NOTE: Equipment, syringes, needles used for vaccination must be clean, sterile and free of chemicals. After use, dismantle and wash in disinfectant such as household bleach (20 mL in 500 mL water) then rinse in cold water. Withholding Periods: Zero (0) days Trade Advice: Export Slaughter Interval (ESI): Zero (0) days Safety Directions: First Aid Instructions: If poisoning occurs, c Read the complete document
PRODUCT NAME: ULTRAVAC BEF VACCINE PAGE: 1 OF 5 This version issued: 8 December 2014 SAFETY DATA SHEET Issued by: Zoetis Australia Pty Ltd Phone: 1800 814 883 POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA SECTION 1 - IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND SUPPLIER ZOETIS AUSTRALIA PTY LTD ABN 94 156 476 425 Level 6, 5 Rider Blvd Rhodes NSW 2138 AUSTRALIA Tel: 1800 814 883 Fax: (02) 8876 0444 Email: australia.animalhealth@zoetis.com CHEMICAL NATURE: Freeze dried live viruses. TRADE NAME: ULTRAVAC BEF VACCINE OTHER NAMES: Ultravac BEF APVMA APPROVAL NUMBER: 41461 RECOMMENDED USE: For the prevention of bovine ephemeral fever by vaccination in cattle. RESTRICTIONS ON USE For veterinary use only. EMERGENCY PHONE: 1800 814 883 (ALL HOURS) CREATION DATE: SEPTEMBER, 2014 THIS VERSION ISSUED: DECEMBER, 2014 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. Not a Dangerous Good according to Australian Dangerous Goods (ADG) Code, IATA and IMDG/IMSBC criteria. RISK PHRASES: Not Hazardous - No criteria found. SAFETY PHRASES: Not Hazardous - No criteria found. SUSMP CLASSIFICATION: S4 ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated GHS CLASSIFICATION: GHS LABEL ELEMENTS: NONE. NOT HAZARDOUS. SIGNAL WORD: NONE. NOT HAZARDOUS. HAZARD STATEMENT: NONE. NOT HAZARDOUS. PREVENTION P102: Keep out of reach of children. P235: Keep cool, preferably between 2 and 8°C, but do not freeze. P262: Do not get in eyes, on skin, or on clothing. P281: Use personal protective equipment as required. RESPONSE P353: Rinse skin or shower with 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. DISPOSAL P501: Discarded vials/containers should immediately be pla Read the complete document