Bimamec 5 mg/ml Pour-On Solution for Cattle
Active ingredient: Ivermectin
Form
Spot-on
Species
Manufacturer
Bimeda Animal Health Limited
VMD MA No.
50146/4044
What it's used for
For the treatment and control of gastro-intestinal nematodes, lungworms, eyeworms, warbles, chorioptic and sarcoptic mange and sucking and biting lice in b...
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Bimamec 5 mg/ml Pour-On Solution for Cattle — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
warbles, chorioptic and sarcoptic mange and sucking and biting lice in beef and non-
lactating dairy cattle.
The product at the recommended dosage level of 500 μg
bodyweight effectively controls the following parasites of cattle:
Gastrointestinal roundworms (adult and fourth stage larvae):
Ostertagia ostertagi
(including inhibited stage)
Haemonchus placei
Trichostrongylus axei T. colubriformis Cooperia
Strongyloides papillosus adult
Trichuris spp. adult
Lungworms (adult and fourth stage larvae):
Dictyocaulus viviparus
Eyeworms (adult):
Thelazia spp.
Revised: January 2024
AN: 02662/2023
Warbles (parasitic stages):
Hypoderma bovis
H. lineatum
Mites:
Sarcoptes scabiei var. bovis
Chorioptes bovis
Lice:
Linognathus vituli
Haematopinus eurysternus
Solenopotes capillatus
Damalinia bovis
The product, given at the recommended dosage of 500 micrograms per kg bodyweight,
controls infections with
after treatment,
the first 21 days after treatment and
the first 28 days after treatment. It also controls horn fly (Haematobia irritans) for up to
35 days after treatment.
Dosage: 1 ml per 10 kg bodyweight (based on a recommended dosage level of 500
micrograms per kg bodyweight).
Administration: 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. To ensure administration of correct dose, body weight
should be determined as accurately as possible; accuracy of the dosing device should
be checked.
excipients.
The product has been formulated for topical application specifically in cattle.
Do not apply or administer to other species as severe adverse reactions, including
fatalities in dogs, may occur.
Do not apply to areas of skin which have mange, scabs or other lesions or to areas
contaminated with mud or manure.
dose rate.
Care should be taken to avoid the following practices because they increase the risk
of development of resistance and could ultimately result in ineffective therapy:
·Too frequent and repeated use of anthelmintics from the same class, over
an extended period of time.
·Underdosing, which may be due to underestimation of body weight, misadministration
of theproduct, or lack of calibration of the dosing device (if any).
Suspected clinical cases of resistance to anthelmintics should be further investigated
using appropriate tests (e.g. Faecal Egg Count Reduction Test). Where the results of
the test(s) strongly suggest resistance to a particular anthelmintic, an anthelmintic
belonging to another pharmacological class and having a different mode of action
should be used.
Resistance to macrocyclic lactones (which includes ivermectin) has been reported in
Cooperia spp. and Ostertagia ostertagi in cattle within the EU.
Revised: January 2024
AN: 02662/2023
Therefore, the use of this and other similar macrocyclic lactone products should be
based on local (regional, farm) epidemiological information about susceptibility of
nematodes and recommendations on how to limit further selection for resistance to
anthelmintics.
Special precautions for use in animals
For external use only.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
HIGHLY FLAMMABLE - KEEP AWAY FROM HEAT, SPARKS, OPEN FLAME OR
OTHER SOURCES OF IGNITION.
The product may be irritating to human skin and eyes and the users should be
careful not to apply it to themselves or others.
Operators should wear rubber gloves and boots with a waterproof coat when
applying the product. Protective clothing should be washed after use.
Use only in well-ventilated areas or outdoors.
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 irritation
persists, seek medical advice and show the package leaflet or label to the physician.
If accidental eye exposure occurs, flush the eyes immediately with water and get
medical attention.
Wash hands after use.
Do not smoke, eat or drink while handling the product.
Other precautions
This product is very toxic to aquatic organisms, sediment dwelling organisms, and dung
insects. Long-term effects on dung insects caused by continuous or repeated use
cannot be excluded.
Treated cattle should not have direct access to ponds, streams or ditches for 14 days
after treatment. The risk to aquatic ecosystems and dung fauna can be reduced by
avoiding too frequent and repeated use of this product and other products of the same
anthelmintic class. Therefore, the repetition of treatment in a pasture during a season
should be performed only in the absence of alternative treatment and on veterinary
advice.
The product may be used concurrently with foot and mouth disease vaccine or
clostridial vaccine.
Bottles should remain upright during storage. Cloudiness may result when the product
is stored at temperatures below 0°C. Allowing the product to warm at room temperature
will restore the normal appearance without affecting efficacy.
Do not use in animals producing milk for human consumption.
Do not use in non-lactating dairy cows including pregnant heifers within 60 days of
calving.
5.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Related Conditions
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