Country: Australia
Language: English
Source: APVMA (Australian Pesticides and Veterinary Medicines Authority)
NORGESTOMET; NORGESTOMET; OESTRADIOL VALERATE
Intervet Australia Pty Limited
norgestomet(1.5mg/mL)+oestradiol valerate(2.5mg/mL)
PARENTERAL IMPLANT, DEVICE
NORGESTOMET STEROID-ANABOLIC Active 3.0 mg/Im; NORGESTOMET STEROID-ANABOLIC Active 3.0 mg/2mL; OESTRADIOL VALERATE STEROID-ESTROGEN Active 5.0 mg/2mL
5 Doses
VM - Veterinary Medicine
INTERVET AUSTRALIA
CATTLE - BEEF | DAIRY CATTLE | DAIRY CATTLE DRY | HEIFER (YOUNG FEMALE CATTLE) | BOVINE | BREEDERS | BULLOCKS | BULLS | CALVES |
ENDOCRINE SYSTEM
CONTROL OF OESTRUS | SYNCHRONISATION OF OESTRUS
Poison schedule: 4; Withholding period: WHP: Meat: DO NOT USE less than 51 days before slaughter for human consumption . Milk: DO NOT USE in cows where milk o r milk products may be used for human consumption.; Host/pest details: CATTLE - BEEF: [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; DAIRY CATTLE: [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; DAIRY CATTLE DRY: [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; HEIFER (YOUNG FEMALE CATTLE): [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; Poison schedule: 4; Withholding period: ; Host/pest details: CATTLE - BEEF: [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; DAIRY CATTLE: [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; DAIRY CATTLE DRY: [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; HEIFER (YOUNG FEMALE CATTLE): [CONTROL OF OESTRUS, SYNCHRONISATION OF OESTRUS]; For oestrus control in beef breeding cattle, maiden dairy heifers & dry (non-lactating) dairy cows in order to apply a planned insemination program.See LIMITATIONS on label
Stopped
2021-07-01
directions for use: read the enclosed leaflet and blister pack before using this product. withholding period: Meat: do not use less than 51 days before slaughter for human consumption. Milk: do not use in cows where milk or milk products may be used for human consumption. trade adVice: EXPORT SLAUGHTER INTERVAL (ESI): This product does not have an ESI established. For advice on the ESI, contact the manufacturer on 1800 033 461 before using this product. warrantY Intervet Australia Pty Ltd (IAPL) warrants that this product is of merchantable quality and fit for its intended purpose. IAPL's liability for any loss, including consequential losses or injury caused by act or omission, including negligent acts or omissions, by IAPL or its agent, is limited to replacing or repairing the product at the option of IAPL. If possible, a sample of any product causing concern should be retained or delivered to IAPL within 30 days for a scientific examination. first aid: if poisoning occurs, contact a doctor or poisons information centre. phone 13 11 26. Storage: Store below 25°C (Air conditioning). Protect from light and moisture. DISPoSaL: Implants must be collected after removal for disposal by incineration. Dispose of empty container, outer packaging or expired product by wrapping with paper and putting in garbage. APVMA Approval No.: 48149/25D/0909 INTERVET AUSTRALIA PTy LIMITED 91-105 Harpin Street BENDIGO EAST VIC 3550 Phone: (03) 54409888 Fax: (03) 5442 3162 LIMItatIoNS: This product is for use in breeding cattle only. Not for use in food producing animals including cows producing milk for human consumption and feedlot cattle. CRESTAR ® is not a cure and should be used only in healthy animals. This product must not be used where contamination of milk is likely. Cows should not be treated until at least 45 days after the last calving. Heifers to be treated should have reached at least 65-70% of their adult weight and should be at least 15-20 months of age depending on breed. The animals should be well fed and in good co Read the complete document
PRODUCT NAME: CRESTAR FOR OESTRUS CONTROL IN BREEDING CATTLE MATERIAL SAFETY DATA SHEET THIS REVISION ISSUED: JULY, 2009 PAGE: 1 OF 6 MATERIAL SAFETY DATA SHEET Issued by: Intervet Australia Pty Limited Phone: 1 800 033 461 (Business Hours) Poisons Information Centre: 13 11 26 from anywhere in Australia, (0800 764 766 in New Zealand) SUBSTANCE: Hormone preparation in a suitable vehicle. TRADE NAME: CRESTAR FOR OESTRUS CONTROL IN BREEDING CATTLE PRODUCT CODE: 22184 OTHER NAMES: This MSDS is intended for both the Implant and the Injectable version of this product. RECOMMENDED USE: A subcutaneous implant and injection for use in cattle for oestrus synchronisation. APVMA NO: 48149 CREATION DATE: November, 2006 THIS VERSION ISSUED: July, 2009 and is valid for 5 years from this date. STATEMENT OF HAZARDOUS NATURE: THIS PRODUCT IS CLASSIFIED AS: Xn, Harmful. Hazardous according to the criteria of SWA. Not a Dangerous Good according to the Australian Dangerous Goods (ADG) Code. RISK PHRASES: R21/22. Harmful in contact with skin and if swallowed. SAFETY PHRASES: S20, S24, S37, S45. When using, do not eat or drink. Avoid contact with skin. Wear suitable gloves. In case of accident or if you feel unwell, contact a doctor or Poisons Information Centre immediately (show the label where possible). SUSDP CLASSIFICATION: S4 ADG CLASSIFICATION: None allocated. Not a Dangerous Good under the ADG Code. UN NUMBER: None allocated PHYSICAL DESCRIPTION & COLOUR: Light yellow oil/Small white cylinder. ODOUR: Mild sesame oil odour/No odour. MAJOR HEALTH HAZARDS: harmful in contact with skin, and if swallowed. Norgestomet has low toxicity but is a potential progestagen and can be skin or gut absorbed. The following is recorded as general properties of progestagens: SIDE EFFECTS : Gastro-intestinal disturbances, acne, fluid retention, weight gain, allergic skin rashes or urticaria, mental depression, breast changes, libido changes, altered liver function and rarely, jaundice. PRECAUTIONS: Mentioned for humans are cautions with pre-existing Read the complete document