Ország: Ausztrália
Nyelv: angol
Forrás: APVMA (Australian Pesticides and Veterinary Medicines Authority)
BISMUTH SUBNITRATE
ZOETIS AUSTRALIA PTY LTD
bismuth subnitrate(650mg/g)
MISC. INTRA MAMMARY
BISMUTH SUBNITRATE MINERAL-BISMUTH Active 650.0 mg/g
120 x 4g; applicator
VM - Veterinary Medicine
ZOETIS AUSTRALIA
DAIRY CATTLE - NON-LACTATING (DRY) PERIO
MISCELLANEOUS VETERINARY
MASTITIS | SUBCLINICAL MASTITIS
Poison schedule: 0; Withholding period: WITHHOLDING PERIOD: MILK: DO NOT USE in lactating cows or within 4 days of calvi ng. After calving, colostrum or milk fro m treated dry cows. MUST NOT BE USED for human consumption or processing for 96 hours (8 milkings). MEAT: ZERO (0) DAY S ESI: ESI not required; Host/pest details: DAIRY CATTLE - NON-LACTATING (DRY) PERIO: [MASTITIS]; For the prevention of clinical & sub-clinical mastitis in dairy cows during the non-lactating (dry) period and early post-calving.DO NOT USE in lactating cows or within 4 days of calving. After calving, colostrum or milk from treated dry cows MUST NOT BE USED for human consumption or processing for 96 hours (8 milkings).
Registered
2023-07-01
Company Name: Product Name: APVMA Approval No: ZOETIS AUSTRALIA PTY LTD TEATSEAL 51357/106869 Label Name: TEATSEAL Signal Headings: FOR ANIMAL TREATMENT ONLY READ SAFETY DIRECTIONS BEFORE OPENING OR USING Constituent Statements: 650 mg/g BISMUTH SUBNITRATE Claims: For the prevention of clinical and subclinical mastitis in dairy cows during the non-lactating (dry) period and early post-calving. Net Contents: 120 x 4g applicator Directions for Use: Restraints: DO NOT USE in lactating cows Dosage and Administration: During the administration of the product it is important to ensure that infection is not introduced. Accidental introduction of bacteria into the quarter during insertion of the intramammary syringe can result in serious mastitis. Thoroughly clean hands prior to administration and wear clean gloves during administration. Immediately after the last milking at drying off, prior to treatment with Teatseal, the udder should be stripped and each teat thoroughly cleaned with a suitable disinfectant. Carefully infuse the entire contents of one injector into each teat to form a seal, preventing the ingress of pathogenic bacteria into the udder during the dry period. After infusion do not massage or squeeze the teat as this may dislodge the seal. It is recommended that Teatseal be used as part of a herd approach to dry cow management and mastitis control. Cows considered likely to be free of subclinical mastitis and at risk for new infection in the dry period should be given Teatseal at drying off. Other animals should be managed in accordance with an approved mastitis control plan or specific veterinary advice. RLP APPROVED For practical purposes, selection criteria may be based on the mastitis and cell count history of individual cows, or recognised tests for the detection of subclinical mastitis, or bacteriological sampling. As a guide, where there has been no episode of clinical mastitis and at least three individual cow cell counts are available, cows with all cell counts below 250,000 cells/mL may be given Olvassa el a teljes dokumentumot
PRODUCT NAME: TEATSEAL PAGE: 1 OF 5 This revision issued: April, 2013 SAFETY DATA SHEET Issued by: Pfizer Animal Health Australia Pty Ltd Phone: 1800 814 883 POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA, (0800 764 766 IN NEW ZEALAND) SECTION 1 - IDENTIFICATION OF THE MATERIAL AND SUPPLIER Pfizer Animal Health Australia Pty Ltd 38-42 Wharf Road West Ryde NSW 2114 Tel: 1800 814 883 Fax: (02) 9850 3399 __________________________________________________________ PFIZER ANIMAL HEALTH AUSTRALIA PTY LTD ABN 94 156 476 425 CHEMICAL NATURE: Veterinary health care product. TRADE NAME: TEATSEAL APVMA CODE: 51357 PRODUCT USE: For the prevention of mastitis in dairy cows during the non-lactating (dry) period. See product label for instructions regarding application. CREATION DATE: MAY, 2002 THIS VERSION ISSUED: APRIL, 2013 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 Australia. 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. SUSMP CLASSIFICATION: None allocated. ADG CLASSIFICATION: None allocated. Not a Dangerous Good. UN NUMBER: None allocated GHS SIGNAL WORD: NONE. NOT HAZARDOUS. PREVENTION P102: Keep out of reach of children. P235: Keep cool. RESPONSE P353: Rinse skin or shower with water. P301+P330+P331: IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P332+P313: If skin irritation occurs: Get medical advice. P337+P313: If eye irritation persists: Get medical advice. P370+P378: Not combustible. Use extinguishing media suited to burning materials. STORAGE P401: Store in the closed original container. DISPOSAL P501: Dispose of small quantities and empty containers by wrapping with paper and putting in garbage. For larger quantities, if recycling or reclaiming is not possible, use a commercial waste disposal service. E E E M M M Olvassa el a teljes dokumentumot