Land: Australien
Sprache: Englisch
Quelle: APVMA (Australian Pesticides and Veterinary Medicines Authority)
INACTIVATED MANNHEIMIA HAEMOLYTICA STRAIN X387; INACTIVATED M. HAEMOLYTICA LEUCOTOXIN STRAIN X332; POLYMYXIN B SULFATE; THIOMERSAL
INTERVET AUSTRALIA PTY LIMITED
Pasteurella haemolytica
PARENTERAL LIQUID/SOLUTION/SUSPENSION
INACTIVATED MANNHEIMIA HAEMOLYTICA STRAIN X387 VACCINE - GENERAL Active 0.0 P; INACTIVATED M. HAEMOLYTICA LEUCOTOXIN STRAIN X332 VACCINE - GENERAL Active 0.0 P; POLYMYXIN B SULFATE ANTIBIOTIC Other 0.1 mg/ml; THIOMERSAL MERCURY Other 0.1 mg/ml
100mL; 250mL; 500mL
VM - Veterinary Medicine
INTERVET AUSTRALIA
CATTLE | BEEF | BOS INDICUS | BOS TAURUS | BOVINE | BUFFALO | BULL | BULLOCK | CALF | COW | DAIRY COW | HEIFER | STEER
IMMUNOTHERAPY
RESPIRATORY DISEASE
Poison schedule: 0; Withholding period: WITHOLDING PERIOD: Nil EXPORT SLAUGHTE R INTERVAL (ESI): ESI not required.; Host/pest details: CATTLE: [RESPIRATORY DISEASE]; An aid in the control of cattle respiratory disease (BRD) caused by Mannheimia haemolytica.See SIDE EFFECTS section on label
Registered
2023-07-01
100 ML INACTIVATED _Mannheimia haemolytica_ Strain x387 (Leucotoxin producing) min. input 1x10 7 orgs/mL Strain x332 min. input 1x10 8 orgs/mL PRESERVATIVES: 0.1 mg/mL Thiomersal 0.1 mg/mL Polymixin B sulphate READ DIRECTIONS FOR USE BEFORE USING THIS PRODUCT. DIRECTIONS FOR USE: SHAKE WELL TO MIX BEFORE USE AND KEEP MIXED DURING USE. EQUIPMENT: The vaccine bottle is designed so that it can be used with an automatic vaccinating gun. To connect bottle to automatic vaccinator attach the plain tube end of the draw-off assembly to the automatic vaccinator and the other end to the bottle. Suspend the bottle from the shoulder by means of the plastic cradle and the carrying strap. Eject air from the vaccinator and tubing until vaccine flows through the needle. CAUTION: DISCARD IF PREVIOUSLY FROZEN. OPENED BOTTLES SHOULD BE USED PREFERABLY WITHIN 24 HOURS OF INITIAL OPENING. RE-OPENING INCREASES THE RISKS OF VACCINE CONTAMINATION. SIDE EFFECTS: Vaccination may cause a small swelling at the site of injection that will eventually resolve. A rise in internal body temperature will also occur, returning to normal within 24-48 hours post-vaccination. This may result in some temporary loss of appetite. USER SAFETY INFORMATION: AVOID ACCIDENTAL INOCULATION. Accidental self-injection may cause inflammatory or allergic response and medical advice should be sought in these cases. Clean the damaged area with a suitable disinfectant and seek medical advice. Batch No.: Expiry Date: Client: Coopers Product Description: Bovilis MH 100mL Carton Scale: 100% Colour: PMS 123 PMS 293 100% Black Keyline: (not to be printed) Uncoated/unvarnished area Size: 105W x 55D x 130mm - overall Size: 332.25 x 274mm Clients Code: CA3837C/02 Agency Code & Version: CAH7593 V6 Last revised: 2/10/09 Signal Heading: Futura Std Bold 5.6 mm Product Name: Futura Std Extra Bold 7.5 mm Body Text: Futura Std Book 2.2 mm Directions for Use: Futura Std Bold 2.2 mm Safety Directions: Futura Std Bold 2.2 mm COOPERS ANIMAL HEALTH A division of Intervet Australia Pty Ltd Lesen Sie das vollständige Dokument
PRODUCT NAME: BOVILIS® MH MANNHEIMIA HAEMOLYTICA VACCINE FOR CATTLE MATERIAL SAFETY DATA SHEET THIS REVISION ISSUED: JULY, 2014 PAGE: 1 OF 6 MATERIAL SAFETY DATA SHEET Issued by: Intervet Australia Pty Limited (known 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: Preparation of inactivated pathogens and preservatives. TRADE NAME: BOVILIS ® MH _MANNHEIMIA HAEMOLYTICA_ VACCINE FOR CATTLE PRODUCT CODE: 3835B RECOMMENDED USE: A vaccine, for use as an aid in the control of respiratory disease in cattle caused by _Mannheimia haemolytica_. For use as described on the product label. APVMA NO: 55767 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: S45. In case of accident or if you feel unwell, contact a doctor or Poisons Information Centre immediately (show the label where possible). SUSDP CLASSIFICATION: None allocated. ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated PHYSICAL DESCRIPTION & COLOUR: Off-white, milky liquid. ODOUR: No 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. In addition product is unlikely to cause any discomfort or irritation. 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 (KNOWN AS MSD ANIMAL HEALTH) 91-105 HARPIN STREET TEL: 1800 226 511 (BUSINESS HOURS) BENDIGO EAST, VIC 3550, AUSTRALIA FAX: 1800 810 511 CO Lesen Sie das vollständige Dokument