Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep
Albendazole
Last verified
Veterinary medicinal product: oral suspension. Distribution category: POM-VPS (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Albendazole.1
In short: questions and answers
- Does Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep need a prescription?
- Status not established. Neither the leaflet nor the law settles how this drug is dispensed, and we do not guess.
- Which animals is Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep for?
- Cattle, Sheep.1
- What is the active substance in Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep?
- Albendazole. ATCvet code: QP52AC11.13
- What is the withdrawal period of Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep according to the leaflet?
- Cattle, meat: 14 days; Cattle, milk: 60 h; Sheep, meat: 4 days.3
- Dispensing
- Status not established
POM-VPS: Prescription Only Medicine - Veterinarian, Pharmacist, Suitably Qualified Person. Prescription only, but the prescription may come from a veterinary surgeon, a pharmacist or a suitably qualified person (SQP, a registered animal-medicine adviser), and they may supply it.12
- Active substance
- Albendazole
- ATCvet code
- QP52AC113
- Manufacturer
- Marketing authorisation holder: Bimeda Animal Health Limited
Withdrawal period
Summary of product characteristics
Composition
| Active substance: | per ml |
|---|---|
| Albendazole | 100 mg |
| Other Relevant Constituents: | |
| Selenium (as sodium selenite) | 1.08 mg |
| Cobalt (as cobalt sulfate) | 2.5 mg |
| Excipients: | |
| Methyl Parahydroxybenzoate (E218) (preservative) | 2 mg |
| Propyl Parahydroxybenzoate (E216) (preservative) | 0.2 mg |
| Acid Brilliant Green BS (E142) (colouring agent) | 0.015 mg |
For a full list of excipients, see section 6.1
6.1 List of excipients
Acid Brilliant Green BS (E142)
Methyl Parahydroxy benzoate (E218)
Propyl Parahydroxy benzoate (E216)
Sodium selenite
Cobalt sulfate
Citric Acid Monohydrate
Sodium Citrate Dihydrate
Xanthan Gum
Povidone
Polysorbate 20
Propylene Glycol
Simethicone Emulsion
Purified Water
Pharmaceutical form
Oral suspension
Pale blue
Pharmacological properties
ATCVet Code: QP52AC11
5.1 Pharmacodynamic properties
A broad spectrum multi-purpose anthelmintic for the control of mature and developing immature forms of gastrointestinal roundworms, lungworms, tapeworms and adult liver fluke in cattle and sheep. The product is also ovicidal against fluke and roundworm eggs.
Albendazole belongs to the benzimidazole class of anthelmintics.
Benzimidazoles bind to nematode tubulin, a protein necessary for the formation and viability of microtubules. This occurs primarily in absorptive intestinal cells resulting in the absence of microtubules in the intestinal cells of the nematode, with the result that these cells cannot absorb nutrients, thus causing a consequent reduction in glycogen and effective starvation of the parasites. Structural differences have been shown to exist between tubulin from mammalian and helminth sources, resulting in the preferential toxicity of albendazole to the helminth and not to the host. Benzimidazoles have also been shown to inhibit the fumarate reductase system of helminths and impair energy production.
The selenium and cobalt are trace elements of use as nutritional supplements and are not intended to be used therapeutically. Administration of ionophores to lambs have been shown to enhance selenium bioavailability. Concurrent administration of ionophores and Ovispec S&C 10 % w/v may therefore lead to an increased risk of selenium toxicity.
Anthelmintic Class: 1-BZ
5.2 Pharmacokinetic particulars
None stated
Target species
Cattle and sheep.
Indications
A broad spectrum multi-purpose anthelmintic for the control of mature and developing, immature forms of gastrointestinal roundworms, lungworms, tapeworms and adult liver fluke in cattle and sheep. The product is also ovicidal against fluke and roundworm eggs.
In Cattle
It is active against the following species:
Roundworms: Teladorsagia, Haemonchus, Trichostrongylus, Nematodirus, Oesophagostomum, Bunostomum, Cooperia and Strongyloides spp. It is usually effective against inhibited larvae of Cooperia and Teladorsagia.
Lungworms: Dictyocaulus viviparus.
Tapeworms: Moniezia spp.
Adult liver fluke: Fasciola hepatica.
The product is ovicidal and will kill fluke and roundworm eggs, thus reducing pasture contamination.
In Sheep
It is active against benzimidazole-susceptible strains of the following species:
Roundworms: Teladorsagia, Haemonchus, Trichostrongylus, Nematodirus (including N. battus), Chabertia and Oesophagostomum. It is usually effective against inhibited larvae of Teladorsagia.
Lungworms: Dictyocaulus filaria.
Tapeworms: Moniezia spp.
Adult liver fluke: Fasciola hepatica.
The product is ovicidal and will kill fluke and roundworm eggs, thus reducing pasture contamination.
Dosage
For oral administration only using properly calibrated dosing equipment. To ensure administration of a correct dose, body weight should be determined as accurately as possible; accuracy of the dosing device should be checked.
Shake the container before use.
Do not mix with other products.
Cattle:
Worm dose
For the control of roundworms, lungworms, tapeworms and fluke and roundworm eggs.
Dosage: 7.5 mg albendazole per kg bodyweight (0.075 ml/kg bodyweight).
Fluke and worm dose
For the additional treatment of adult liver fluke (chronic fascioliasis) in cattle.
Dosage: 10 mg albendazole per kg bodyweight (0.1 ml/kg bodyweight).
Sheep:
Worm Dose
For the control of roundworms, lungworms, tapeworms and fluke and roundworm eggs.
Dosage: 5 mg albendazole per kg bodyweight (0.05 ml/kg bodyweight).
Fluke and Worm Dose
For the additional treatment of adult liver fluke (chronic fascioliasis) in sheep.
Dosage: 7.5 mg albendazole per kg bodyweight (0.075 ml/kg bodyweight).
Administration with a suitable drenching gun is recommended (see 4.5).
Contraindications
Do not use in animals with known hypersensitivity to the active ingredient.
Adverse reactions
None known.
Warnings
Avoid the introduction of contamination during use.
The product should only be used in areas where deficiencies of cobalt and selenium are likely to occur. If in any doubt, seek the advice of a veterinary surgeon.
i) Special precautions for use in animals
Care must be taken not to damage the pharyngeal region when dosing, particularly in sheep.
Do not administer other cobalt and selenium supplements concurrently unless specifically advised by your vet. Not to be diluted.
ii) Special precautions to be taken by the person administering the veterinary medicinal product to animals
Avoid direct contact with the product.
Wear suitable protective clothing including impermeable rubber gloves. In the event of accidental eye exposure, flush eye thoroughly with running water. If irritation persists, seek medical attention. In the event of accidental skin exposure, wash the affected areas with soap and water. If irritation persists, seek medical attention. Wash hands after use.
Use during pregnancy, lactation or lay
The use of the product in breeding bulls or pregnant cattle is not expected to interfere with their reproductive performance.
Do not dose ewes at the ‘fluke and worm’ dose rate (7.5 mg/kg), during tupping or for 1 month after removing the rams.
Ovispec S&C 10 % w/v can be safely used during lactation.
Interactions
Administration of ionophores to lambs has been shown to enhance selenium bioavailability. Concurrent administration of ionophores and the product may therefore lead to an increased risk of selenium toxicity.
Overdose
Benzimidazoles have a wide safety margin.
Special warnings
Cattle suffering from severe lung damage due to heavy lungworm infestation may continue to cough for some weeks after dosing.
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 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 benzimidazoles (which includes albendazole) has been reported in Teladorsagia, Haemonchus, Cooperia and Trichostrongylus species in small ruminants in a number of countries, including the EU. Resistance to albendazole has been reported in Cooperia and Teladorsagia species in cattle in developed countries such as in New Zealand. Therefore the use of this product 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.
To reduce this risk, dosing programmes should be discussed with a veterinary surgeon.
Withdrawal period
Cattle:
Meat: 14 days
Milk: 60 hours
Sheep:
Meat: 4 days
Milk: Do not use in sheep producing milk for human consumption.
Incompatibilities
None known
Immediate packaging
1.0, 2.5 and 5.0 litre white high density polyethylene back pack with white high density polyethylene cap (screw fit).
10.0 litres high density polyethylene jerricans with white high density polyethylene cap (screw fit) with induction reseal liner.
Not all pack sizes may be marketed.
Storage
Do not store above 25 °C.
Shelf life
Shelf life of the veterinary medicinal product as packaged for sale: 18 months
Disposal of unused product
DANGEROUS to fish and aquatic life.
Do not contaminate ponds, waterways or ditches with the product or used containers.
Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal product should be disposed of in accordance with local requirements.
Additional information
Vm 50146/4032
9 DATE OF FIRST AUTHORISATION
17 December 2001
10 DATE OF REVISION OF THE TEXT
April 2026
Gavin Hall Approved: 06 May 2026
Registration holder
Bimeda Animal Health Limited
2 / 3 / 4 Airton Close
Tallaght
Dublin 24
Ireland
Regulations
- Veterinary Medicines Regulations 2013 (SI 2013/2033), Schedule 32
Sources
- VMD Product Information Database: Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep, 50146/4032
- The Veterinary Medicines Regulations 2013, Schedule 3 (categories of veterinary medicinal products)
- Summary of Product Characteristics: Ovidrench S & C 10% w/v Oral Suspension for Cattle and Sheep
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