Nexmectin 18.7 mg/g Oral Paste for Horses
Active ingredient: Ivermectin
Form
Paste
Species
Manufacturer
ACME DRUGS s.r.l.
VMD MA No.
61301/3003
What it's used for
Treatment of nematode or arthropod infection due to: Large strongyles: Strongylus vulgaris (adults and L 4 stage larvae [arterial]) Strongylus edentatus (a...
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Nexmectin 18.7 mg/g Oral Paste for Horses — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
Large strongyles:
Strongylus vulgaris (adults and L 4 stage larvae [arterial])
Strongylus edentatus (adults and L 4 stage larvae [tissue])
Strongylus equinus (adults)
Small strongyles (including benzimidazole resistant strains):
Cyathostomum 4 stage larvae)
Cylicocyclus spp. (adults and luminal L 4 stage larvae)
Cylicodontophorus spp. (adults and luminal L 4 stage larvae)
Cylicostephanus spp. (adults and luminal L 4 stage larvae)
Gyalocephalus spp. (adults and luminal L 4 stage larvae)
Ascarids:
Parascaris equorum (luminal L 5 larvae and adults)
Revised: August 2025
AN: 01416/2025
Pinworms:
Oxyuris equi 4 stage larvae and adults)
Neck threadworms:
Onchocerca
Stomach bots:
Gasterophilus spp. (oral and gastric stages)
One syringe division of paste per 100 kg body weight (based on a recommended
dosage of 200 μg ivermectin per kg body weight).
The syringe containing 6.42 g of paste delivers sufficient paste to treat 600 kg of
bodyweight at the recommended dose rate.
The syringe containing 7.49 g of paste delivers sufficient paste to treat 700 kg of
bodyweight at the recommended dose rate.
Administration:
The paste is given by oral route.
Revised: August 2025
AN: 01416/2025
To ensure administration of a correct dose, body weight should be determined as
accurately as possible. The animal’s mouth should be free from food to ensure
swallowing. Turn the screw gauge on the syringe plunger to the body weight of the
horse. The tip of the syringe barrel should be inserted at the interdental space (the
gap between the front and back teeth) and the paste deposited on the base of the
tongue. Advance the plunger as far as it will go, depositing the medication on the
base of the tongue. Immediately elevate the horse’s head for a few seconds to
ensure swallowing.
excipients.
Do not use in dogs or cats as severe adverse reactions may occur.
experienced oedema and pruritus following treatment, such reactions are assumed to
be the result of death of large numbers of microfilariae. These signs resolve within a
few days but symptomatic treatment may be advisable.
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:
•
extended period of time.
•
misadministration of the product.
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.
Veterinary advice should be given on appropriate dosing programs and stock
management to achieve adequate parasite control and reduce the likelihood of
anthelmintic resistance developing. In the event that a product is suspected of being
ineffective, the animal owner is advised to seek veterinary advice.
Resistance to ivermectin has been reported in Parascaris equorum. Therefore, the
use of this product should be based on local 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
Since ivermectin is highly bound to plasma proteins, special care should be taken in
cases of sick animals or in nutritional conditions associated with low plasma protein
levels.
Revised: August 2025
AN: 01416/2025
Dogs and cats should not be allowed to ingest spilled gel or have access to used
packaging due to the potential for adverse effects related to ivermectin toxicity
The product has been formulated for use in horses only. Cats, dogs (especially
Collies, Old English Sheepdogs and related breeds or crosses) and also turtles and
tortoises may be adversely affected by the concentration of ivermectin in this product
if they are allowed to ingest spilled paste or have access to used syringes.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Do not smoke, eat or drink while handling the product.
Wash hands after use.
This product may cause skin and eye irritation. Therefore, the user should avoid
contact of the product with the skin and the eyes. In case of contact, rinse
immediately with plenty of water.
In the case of accidental ingestion or eye irritation after contact seek medical advice
immediately and show the package leaflet or the label to the physician.
Do not use in mares producing milk for human consumption.
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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Other Products Containing Ivermectin
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Alomec 18.7 mg/g Oral Paste for Horses
POM-VPSBimeda Animal Health Limited
Aloquantel Ivermectin and Praziquantel Oral Gel for Horses
POM-VPSVirbac
Animec 0.5% w/v Pour-on Solution
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Animec 0.5% w/v Pour-on Solution
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Animec 0.8mg/ml Oral Solution for Sheep
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
Animec 10 mg/ml Solution for Injection for Cattle, Pigs and Sheep
POM-VPSChanelle Pharmaceuticals Manufacturing Ltd
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