Animec Pour-on Solution 0.5%

Introduction

Chanelle Vet UK Ltd

Address: CBX11 West Wing

382-390 Midsummer Boulevard

Milton Keynes, Bucks MK9 2RG

Telephone: 01908 843636

Fax: 01908 847401

Website: www.chanellevetuk.com

 

Company name: Chanelle Animal Health Limited

7 Rodney Street

Liverpool

L1 9HZ

Tel & Fax: 01568 750432

Website: www.chanellegroup.ie

Presentation

A clear pour-on solution containing ivermectin 0.5%w/v (5mg/ml).

Uses

Animec Pour-on Solution 0.5% at the recommended dose rate of 500 micrograms ivermectin per kg bodyweight is used for the treatment of the following species of gastrointestinal roundworms, lungworms, warbles, mites and lice in cattle.

Gastro-intestinal roundworms (adults and fourth stage larvae):

Ostertagia ostertagi (including inhibited O ostertagi)

Haemonchus placei

Trichostrongylus axei

Trichostrongylus colubriformis

Cooperia spp

Oesophagostomum radiatum

Strongyloides papillosus (adult)

Trichuris spp (adult)

Lungworms (adult and fourth stage larvae):

Dictyocaulus viviparus

Eye worms (adult):

Thelazia spp

Warbles (parasitic stages):

Hypoderma bovis

Hypoderma lineatum

Mites:

Chorioptes bovis (reduction of infestation)

Sarcoptes scabiei var bovis

Sucking lice:

Linognathus vituli

Haematopinus eurysternus

Biting Lice:

Damalinia bovis

The product given at the recommended dose rate of 500 micrograms/kg bodyweight has persistent activity against Trichostrongylus axei and Cooperia spp. acquired during the 14 days after treatment, only if the whole herd is treated simultaneously; Ostertagia ostertagi and Oesophagostomum radiatum acquired during the first 21 days after treatment; Dictyocaulus viviparus acquired during the first 28 days after treatment. It also has a persistent activity against horn flies (Haematobia irritans) for 28 days after treatment, partial efficacy may last for up to 35 days post application. Occasionally variable activity may be observed against Haemonchus placei (L4), Cooperia spp, Trichostrongylus axei and Trichostrongylus colubriformis.

Dosage and administration

For single topical administration.

Dosage: 1ml per 10kg bodyweight (based on a recommended dosage level of 500 micrograms/kg bodyweight).

Administration: Pour-on use. The formulation should be applied along the mid-line of the back in a narrow strip between the withers and tailhead. The product should be used with appropriate dosing equipment. The interval between 2 treatments should be at least 28 days.

Contra-indications, warnings, etc

Highly flammable - keep away from heat, sparks, open flame or other sources of ignition.

For animal treatment only.

No sign of toxicity appeared up to 1.5mg/kg (3 times the recommended dose rate). No antidote has been identified.

Do not use in cases of known hypersensitivity to the active ingredient.

Frequent and repeated use may lead to the development of resistance. To avoid secondary reactions due to the death of Hypoderma larvae in the oesophagus or in the spine, it is recommended to administer the product at the end of the period of warble fly activity and before the larvae reach their resting site. Do not treat cattle when hair or hide is wet. Do not treat cattle if rain is expected, as rain within 2 hours of treatment may reduce efficacy. However, the efficacy of the product against established infections of O. ostertagi or D. viviparus is not adversely affected if the hide is wet or if rain falls shortly after treatment.

Do not apply to areas of skin which have mange scabs or other lesions or to areas contaminated with mud or manure.

The influence of extreme climatic conditions on persistent activity of the product is unknown.

The product has been formulated for topical application specifically for cattle. It should not be administered to other species as severe adverse reactions, including fatalities in dogs, may occur.

Withdrawl periods: Animals must not be slaughtered for human consumption during treatment. Cattle may be slaughtered for human consumption only after 28 days from the last treatment.

Do not use in cows producing milk for human consumption.

Do not use in non-lactating dairy cows including pregnant heifers within 60 days of calving.

Standard Operator Warnings:The product may be irritating to human skin and eyes and the user should be careful not to apply it to himself or other persons. Operators should wear rubber gloves and boots with a waterproof coat when applying the product. Protective clothing should be washed after use. As absorption through skin can occur, in the event of accidental skin contact the affected area should be washed immediately with soap and water. If accidental eye exposure occurs, flush the eyes immediately with water and seek medical attention. Do not eat, drink or smoke whilst handling the product. Wash hands after use. Use only in well-ventilated areas or outdoors.

Container Disposal: EXTREMELY DANGEROUS TO FISH AND AQUATIC LIFE. Do not contaminate surface waters or ditches with the product or used container. Dispose of any unused product and empty containers in accordance with guidance from your local waste regulation authority.

Pharmaceutical precautions

Highly flammable - keep away from heat, sparks, open flame or other sources of ignition. Close container when not in use. Bottles should remain upright during storage. Protect from light.

Legal category

POM-VPS

Packaging Quantities

High density polyethylene containers(flat bottomed flexi packs) with tamper evident closures.

Pack sizes: 1L, 2.5L, 5L & 6L(consisting of 5L & 1L packs).

Or

High density polyethylene squeeze measure pour containers with child resistant closures.

Pack sizes: 250ml, 500ml & 1L.

Further information

The product can be administered to beef cows at any stage of pregnancy or lactation provided that the milk is not intended for human consumption. Not permitted for use in lactating animals producing milk for human consumption. The product will not affect the fertility of cows and bulls and can be given to all ages of animals including young calves.

Marketing authorisation number

Vm 11990/4038.