Երկիր: Ավստրալիա
Լեզու: անգլերեն
Աղբյուրը: APVMA (Australian Pesticides and Veterinary Medicines Authority)
NEOMYCIN SULFATE; NOVOBIOCIN AS NOVOBIOCIN SODIUM; DIHYDROSTREPTOMYCIN
ZOETIS AUSTRALIA PTY LTD
neomycin as sulfate(10.5mg/mL)+novobiocin as Na salt(10mg/mL) + others
MISC. INTRA MAMMARY
NEOMYCIN SULFATE ANTIBIOTIC Active 150.0 mg/10ml; NOVOBIOCIN AS NOVOBIOCIN SODIUM ANTIBIOTIC Active 100.0 mg/10ml; DIHYDROSTREPTOMYCIN ANTIBIOTIC Active 100.0 mg/10ml
20 x 10mL; plastets
VM - Veterinary Medicine
ZOETIS AUSTRALIA
DAIRY CATTLE LACTATING | BOVINE | MILKING COW
ANTIBIOTIC & RELATED
MASTITIS | SUBCLINICAL MASTITIS
Poison schedule: 4; Withholding period: WHP: Do not use less than 30 days befor e slaughter for human consumption. Mil k collected from cows within 72 hours ( 6 milkings) following treatment must no t be used for human consumption or pro cessing. This milk should not be fed t o bobby calves.; Host/pest details: DAIRY CATTLE LACTATING: [MASTITIS]; For the treatment of bovine mastitis, in lactating dairy cattle only by intramammary infusion..Milk from treated cows should not be fed to bobby calves (See WITHHOLDING PERIODS statement on label).
Registered
2023-07-01
Veterinary Labelling Special Formula 17900 Forte V Lactating lntramammary Antibiotic Suspension LABEL TEXT- PLASTET SYRINGE Main Panel PRESCRIPTION ANIMAL REMEDY KEEP OUT OF REACH OF CHILDREN FOR ANIMAL TREATMENT ONLY Special Formula 17900 Forte-V Lactating lntramammary Antibiotic Suspension Each 1 Oml PLASTET"' contains NEOMYCIN (as neomycin sulphate) NOVOBIOCIN 105mg 100mg (as novobiocin sodium) DIHYDROSTREPTOMYCIN (as the sulphate) 100mg For the treatment of bovine mastitis. 1 Oml PLASTET'" Disposable Syringe Store below 25°C (Air- conditioning) Batch: Expiry: Right Hand Side Panel READ THE CARTON BEFORE USING THIS PRODUCT DIRECTIONS FOR USE SHAKE WELL BEFORE USE Infuse one PLASTEr'" (10ml) per infected quarter. WITHHOLDING PERIODS DO NOT USE less than 30 days before slaughter for human consumption. APVMA Page 1 of 4 15 1 h July 2013 + RLP Approved Milk collected from cows within 72 hours (6 milkings) following treatment MUST NOT BE USED for human consumption or processing. This milk should not be fed to bobby calves. APVMA Approval No. 38696 I 60502 Zoetis Australia Pty Ltd 38-42 Wharf Road West Ryde, NSW 2114 LABEL Veterinary Labelling SPECIAL FORMULA 17900 FORTE-V LACTATING LNTRAMAMMARY ANTIBIOTIC SUSPENSION Main Panel PRESCRIPTION ANIMAL REMEDY KEEP OUT OF REACH OF CHILDREN FOR ANIMAL TREATMENT ONLY SPECIAL FORMULA 17900 FORTE-V CARTON TEXT LACTATING LNTRAMAMMARY ANTIBIOTIC SUSPENSION Each 1 OmL PLASTETN contains NEOMYCIN (as neomycin sulphate) NOVOBIOCIN (as novobiocin sodium) DIHYDROSTREPTOMYCIN (as the sulphate) APVMA Page 2 of 4 15 July 2013 105MG 100MG 100MG For the treatment of bovine mastitis, in lactating cattle only, by intramammary infusion. 20 x 1 OmL PLASTET'" Disposable Syringes [Zoetis logo] Right Hand Side Panel DIRECTIONS FOR USE DOSAGE: SHAKE WELL BEFORE USE Infuse one PLASTET'" (1 OmL) per infected quarter. One 1 OmL infusion of Special Formula 17900 Forte-V into the affected quarter generally will be sufficient. Repeat treatments at 24 or 48 hour intervals, if necessary. 1.Milk the udde Կարդացեք ամբողջական փաստաթուղթը
PRODUCT NAME: SPECIAL FORMULA 17900 FORTE-V ® PAGE: 1 OF 4 THIS REVISION ISSUED: NOVEMBER 2010 MATERIAL SAFETY DATA SHEET Issued by: Pfizer Australia Pty Ltd Phone: (02)9850 3333 SECTION 1 - IDENTIFICATION OF CHEMICAL PRODUCT AND COMPANY Pfizer Australia Pty Ltd 38-42 Wharf Road West Ryde NSW 2114 Tel: (02) 9850 3333 Fax: (02) 9850 3399 ____________________________________ PFIZER AUSTRALIA PTY LTD A.B.N. 50 008 422 348 SUBSTANCE: Active ingredients are antibiotics. TRADE NAME: SPECIAL FORMULA 17900 FORTE-V ® PFIZER MSDS CODE: 101 PRODUCT USE: For the treatment of bovine mastitis in lactating cattle only, by mammary infusion. CREATION DATE: MARCH, 2005 THIS VERSION ISSUED: NOVEMBER, 2010 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. SUSDP CLASSIFICATION: S4 ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated E E E M M M E E E R R R G G G E E E N N N C C C Y Y Y O O O V V V E E E R R R V V V I I I E E E W W W PHYSICAL DESCRIPTION & COLOUR: A pale yellow oily suspension. ODOUR: No data. MAJOR HEALTH HAZARDS: no significant risk factors have been found for this product. P P P O O O T T T E E E N N N T T T I I I A A A L L L H H H E E E A A A L L L T T T H H H E E E F F F F F F E E E C C C T T T S S S Possible effects of overexposure to antibiotics in the workplace include: symptoms of hypersensitivity (such as skin rash, hives, itching, and difficulty breathing); nausea; vomiting; diarrhoea. INHALATION SHO Կարդացեք ամբողջական փաստաթուղթը