WEBSTERS 6 IN 1 SE VACCINE

Country: Australia

Language: English

Source: APVMA (Australian Pesticides and Veterinary Medicines Authority)

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Patient Information leaflet (PIL)

12-01-2023

Summary of Product characteristics (SPC)

01-07-2013

Active ingredient:

SELENIUM AS SODIUM SELENATE; CLOSTRIDIUM CHAUVOEI - TOXOID; CLOSTRIDIUM NOVYI TYPE B - TOXOID; CLOSTRIDIUM PERFRINGENS TYPE D TOXOID; CLOSTRIDIUM SEPTICUM - TOXOID; CLOSTRIDIUM TETANI - TOXOID; CORYNEBACTERIUM PSEUDOTUBERCULOSIS - TOXOID; THIOMERSAL

Available from:

VIRBAC (AUSTRALIA) PTY LTD

INN (International Name):

Corynebacterium pseudotubercul(1u/mL) + others

Pharmaceutical form:

MISC. VACCINES OR ANTI SERA

Composition:

SELENIUM AS SODIUM SELENATE MINERAL-SELENIUM Active 1.0 mg/ml; CLOSTRIDIUM CHAUVOEI - TOXOID VACCINE-TOXOID Active 0.0 IU/ml; CLOSTRIDIUM NOVYI TYPE B - TOXOID VACCINE-TOXOID Active 3.5 IU/ml; CLOSTRIDIUM PERFRINGENS TYPE D TOXOID VACCINE-TOXOID Active 5.0 IU/ml; CLOSTRIDIUM SEPTICUM - TOXOID VACCINE-TOXOID Active 2.5 IU/ml; CLOSTRIDIUM TETANI - TOXOID VACCINE-TOXOID Active 2.5 IU/ml; CORYNEBACTERIUM PSEUDOTUBERCULOSIS - TOXOID VACCINE-TOXOID Active 1.0 IU/ml; THIOMERSAL MERCURY Other 0.13 mg/ml

Units in package:

200mL; 500mL

Class:

VM - Veterinary Medicine

Manufactured by:

VIRBAC

Therapeutic group:

LAMB | OVINE

Therapeutic area:

IMMUNOTHERAPY

Therapeutic indications:

Product summary:

Poison schedule: 6; Withholding period: Zero (0) Days Zero (0) Days; Host/pest details: LAMB: [BLACK DISEASE, BLACKLEG, CHEESY GLAND, ENTEROTOXAEMIA (PULPY KIDNEY), MALIGNANT OEDEMA, TETANUS, UNTHRIFTINESS, WHITE MUSCLE DISEASE]; Poison schedule: 6; Withholding period: WHP: Nil ESI: Not Required.; Host/pest details: LAMB: [BLACK DISEASE, BLACKLEG, CHEESY GLAND, ENTEROTOXAEMIA (PULPY KIDNEY), MALIGNANT OEDEMA, TETANUS, UNTHRIFTINESS, WHITE MUSCLE DISEASE]; Prevention of cheesy gland caused by C. pseudotuberculosis, enterotoxaemia caused by CI. perfringens type D, blackleg caused by CI. chauvoei, malignant oedema caused by CI. septicum, black disease caused by CI. novyi type B, tetanus caused by CI tetani…This product should NOT be used when selenium intake from pasture is high or selenium is provided by other means (e.g. pasture top dressing, vaccine, pellets or drenches), or if blood selenium levels at treatment are high.

Authorization status:

Registered

Authorization date:

2023-07-01

Patient Information leaflet

Product Name:
APVMA Approval No:
WEBSTERS 6 IN 1 SE VACCINE
51337/134041
Label Name:
WEBSTERS 6 IN 1 SE VACCINE
Signal Headings:
POISON
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL TREATMENT ONLY
Constituent
Statements:
Contains aluminium adjuvanted toxoid and cellular antigen from
Corynebacterium
pseudotuberculosis (ovis) 1.0 U/mL, Clostridium perfringens type D 5.0
IU/mL, Cl. novyi
type B 3.5 IU/mL, Cl. tetani 2.5 IU/mL, Cl. septicum 2.5 IU/mL, Cl.
chauvoei ≥ 0.3% PCV/
mL and Selenium (as sodium selenate) 1 mg/mL.
0.13 mg/mL of thiomersal added as a preservative.
Claims:
For the prevention of cheesy gland (C. pseudotuberculosis), pulpy
kidney (Cl. perfringens
type D), black disease (Cl. novyi type B), malignant oedema (Cl.
septicum), tetanus
(Cl.tetani) and blackleg (Cl. chauvoei) in sheep and lambs and the
selenium responsive
conditions, white muscle disease and unthriftiness in lambs.
Net Contents:
200mL
500mL
Directions for Use:
Restraints:
Contraindications:
This product should not be used when selenium intake from pasture is
high or selenium
is provided by other means (such as pasture top dressing, vaccine,
pellets or selenium
drenches) or if blood selenium levels at treatment are high. Users can
determine selenium
status by consulting their veterinarian.
Precautions:
Side Effects: RLP APPROVED
Dosage and
Administration:
Shake well before use and keep thoroughly mixed during use.
Use the contents within 50 days of first broaching the pack.
Discard the unused portion.
Handle aseptically and follow resealing and storage instructions.
Dosage: 1 mL dose by subcutaneous injection (under the skin, NOT into
the muscle).
Lambs: 1 mL dose at marking followed by a second 1 mL dose 4 to 6
weeks later. An
annual booster dose will maintain a high level of immunity.
Ewes (fully vaccinated as lambs): 1mL annual booster dose. Administer
2 to 3 weeks
before lambing if possible. This will ensure that high levels of
protective antibodies are
passed to the lambs in colostrum to protect them in their first 6
weeks of life and at

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Summary of Product characteristics

VIRBAC (AUSTRALIA) PTY. LTD.
MATERIAL SAFETY DATA SHEET
Product
Name:
Websters Low Volume 6 in 1 Vaccine with Selenium (including Cheesy
Gland) for Lambs
PAGE: 1 OF 5
DATE OF ISSUE
1 FEBRUARY 2010

EMERGENCY: VIRBAC: 02 9772 9772 OR 1800 242 100 (BUSINESS HOURS
ONLY)
POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA, (0800
764 766 IN NEW ZEALAND)

SECTION 1 - IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY
COMPANY:
VIRBAC (AUSTRALIA) PTY. LTD
ABN 77 003 268 871

ADDRESS
361 Horsley Rd, Milperra, NSW 2214, Australia

Locked Bag 6000, Milperra Business Centre, NSW 1891, Australia
TELEPHONE:
(02) 9772 9772 or 1800 242 100
FAX:
(02) 9772 9773
EMERGENCY PHONE
As above during business hours; answering machine after hours
SUBSTANCE:
Water solution of ingredients including Selenium and
inactivated Clostridial bacteria.

TRADE NAME:
WEBSTERS LOW VOLUME 6 IN 1 VACCINE WITH SELENIUM (INCLUDING
CHEESY
GLAND) FOR LAMBS
OTHER NAMES:
LV 6 in 1 Plus Se
APVMA CODE: 51337
PRODUCT USE:
Vaccination against five clostridial diseases and Cheesy Gland, and
prevention of
selenium responsive conditions in lambs.

CREATION DATE:
FEBRUARY, 2010
REVISION DATE:
DECEMBER, 2010

SECTION 2 - HAZARDS IDENTIFICATION
STATEMENT OF HAZARDOUS NATURE
This product is classified as: Not classified as hazardous
according to the criteria of ASCC.
Not a Dangerous Good according to the Australian Dangerous Goods
(ADG) Code.
RISK PHRASES: Not Hazardous - No criteria found.
SAFETY PHRASES: Not Hazardous - No criteria found.
SUSDP CLASSIFICATION: S6
ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the
ADG Code.
UN NUMBER: None allocated
EMERGENCY OVERVIEW
PHYSICAL DESCRIPTION & COLOUR: Fluid bacterial vaccine in a vial.
ODOUR: No data.
MAJOR HEALTH HAZARDS: no significant risk factors have been found for
this product.
POTENTIAL HEALTH EFFECTS
NOTE: DIFFERENT HAZARD ASSESSMENT CR

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