Eqvalan Gold, Oral Paste
Active ingredients: Ivermectin, Praziquantel
Form
Paste
Species
Manufacturer
Boehringer Ingelheim Vetmedica GmbH
VMD MA No.
61700/3006
What it's used for
For the treatment of mixed cestode and nematode or arthropod infestations in horses. The following parasites of horses are sensitive to the antiparasitic e...
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Prescription required
Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.
Eqvalan Gold, Oral Paste — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
horses. The following parasites of horses are sensitive to the antiparasitic
effects of the product:
Adult Tapeworms:
Anoplocephala perfoliata
Anoplocephala magna
Large strongyles:
Strongylus vulgaris
Strongylus edentatus
Strongylus equinus
Triodontophorus
Triodontophorus brevicauda
Triodontophorus serratus
Craterostomum acuticaudatum
Revised: December 2025
AN: 02368/2025Page 2 of 7
Adult and immature (intraluminal fourth-stage larvae) of small strongyles
or cyathostomes, including benzimidazole-resistant strains:
Coronocyclus
Coronocyclus coronatus
Coronocyclus labiatus
Coronocyclus labratus
Cyathostomum
Cyathostomum catinatum
Cyathostomum pateratum
Cylicocyclus
Cylicocyclus ashworthi
Cylicocyclus elongatus
Cylicocyclus insigne
Cylicocyclus leptostomum
Cylicocyclus nassatus
Cylicodontophorus
Cylicodontophorus bicornatus
Cylicostephanus
Cylicostephanus calicatus
Cylicostephanus goldi
Cylicostephanus longibursatus
Cylicostephanus minutus
Parapoteriostomum
Parapoteriostomum mettami
Petrovinema
Petrovinema poculatum
Poteriostomum
Adult hairworms
Adult and immature (fourth stage Larvae) pinworms
Adult, third- and fourth-stage larvae of roundworms
equorum
Microfilariae of neck threadworms
Adult intestinal threadworms
Adult large-mouth stomach worms
Oral and, gastric stages of bots
Adult and immature (inhibited fourth stage larvae) lungworms
arnfieldi
and 1mg praziquantel per kilogram of bodyweight corresponding to 1.29 g of
paste per 100 kg bodyweight in a single administration.
Bodyweight and dosage should be accurately determined prior to treatment.
The contents of one syringe will treat horses up to 600 kg. Calibrated markings
are provided at 100 kg bodyweight intervals. The syringe should be adjusted to
the calculated dosage by setting the ring on the appropriate place on the
plunger.
Directions for use
The product is for oral administration only. While holding the plunger, turn the
knurled ring on the plunger ¼ turn to the left and slide it so the stop ring is at the
prescribed weight marking. Lock the ring in place by turning it ¼ turn to the right
in order to bring the two arrows, the one visible on the ring and the one on the
plunger rod, into alignment. Make sure the horse’s mouth contains no feed.
Remove the cover from the tip of the syringe. Insert the syringe tip into the
horse’s mouth at the interdental space and deposit the paste on the base of the
tongue. Immediately raise the horse’s head for a few seconds after dosing and
ensure that the paste is consumed.
Parasite control Program
Veterinary advice should be given on appropriate dosing programs and stock
management to achieve adequate parasite control for both tapeworm and
roundworm infestations.
Revised: December 2025
AN: 02368/2025Page 5 of 7
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
Revised: December 2025
AN: 02368/2025Page 3 of 7
experienced oedema and pruritis following treatment; such reactions were
assumed to be the result of the death of large numbers of microfilariae. These
signs resolve within a few days but symptomatic treatment may be advisable.
In cases of heavy infestations with tapeworms, signs of mild, transient colic and
loose stool may be observed.
Revised: December 2025
AN: 02368/2025Page 4 of 7
Following administration of the product, there have been rare reports of
inflammation of the mouth, lip and tongue, which results in various clinical signs
such as oedema, hypersalivation, erythema, tongue disorder and stomatitis.
These reactions have been transitory in nature, appearing within 1 hour and
abating within 24 to 48 hours following administration.In case of severe oral
reactions symptomatic treatment is recommended
risk of development of resistance and could ultimately result in ineffective
therapy:
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an extended period of time.
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misadministration of the product, 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 Parascaris equorum in horses in the EU. Therefore the use of this
product should be based on local (regional, farm) epidemiological information
about susceptibility of gastro-intestinal nematodes and recommendations on
how to limit further selection for resistance to anthelmintics
i. Special precautions for use in animals
Safety studies were not conducted in foals younger than 2 months of age, or in
stallions, the use of the product is not recommended in these categories of
animals.
ii. Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Wash hands after use.
Do not smoke, drink or eat while handling the product.
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 insert or the label to the physician.
Revised: December 2025
AN: 02368/2025Page 7 of 7
Excipients:
Butylhydroxyanisole (E320): 0.002 g
Sunset Yellow (E110): 0.003 g
Titanium dioxide (E171): 0.155 g
For the full list of excipients, see section
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
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