Protect Oral Suspension for New Born Calves

Composition

Active substances:

Lactobacillus acidophilus strain LA-101

Lactobacillus acidophilus strain LA-107

Enterococcus Faecium strain SF-101

Minimum content of each strain is more than 1.0 x 10⁸ cfu/ml at time of use.

For the full list of excipients see section 6.1

6.1 List of excipients

Sunflower Oil

Silica colloidal anhydrous (Aerosil 380)

Orange Oil (Sweet)

Polysorbate 80

Dried yeast

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Pharmaceutical form

Oral suspension

Light brown viscous suspension for oral administration

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Pharmacological properties

Pharmacotherapeutic group: Antidiarrhoeal microorganisms, lactic acid producing organisms, combinations.

ATC Vet code: QA07FA51.

The product contains a combination of three bacterial strains:

Lactobacillus acidophilus strain LA-101

Lactobacillus acidophilus strain LA-107

Enterococcus faecium strain SF-101

These probiotics have been demonstrated to benefit the host animal by positively influencing the intestinal flora.

The three strains of lactic acid forming bacteria used in the product have all been shown, in vitro, to be inhibitory to 8 pathogens common to farm animals. The pathogens tested were: E coli strains K88 and K99, Salmonella typhimurium, dublin and enteritidis ; Staphylococcus aureus, Clostridium perfringens and Listeria monocytogenes.

The organisms may produce a beneficial effect on an animal by influencing microbial metabolism in the gut or suppressing levels of harmful bacteria. Mechanisms of action of probiotic cultures to reduce levels of pathogens have been proposed. These include production of inhibitory substances and increased competition for adhesion sites in the alimentary tract.

5.1 Pharmacodynamic properties

Not yet defined.

5.2 Pharmacokinetic properties

Not yet defined.

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Target species

Calves in their pre-ruminant phase, up to the age of 12 weeks.

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Indications

For use as an aid in the prevention of bacterial diarrhoea in young calves, up to the age of 12 weeks.

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Dosage

Shake the bottle before use.

Prime the automatic dose dispenser by inverting the bottle after attachment and gently squeezing the pump.

Shake the container before administering each dose.

Do not mix the contents or rinse the dispenser with water.

A dose of 5ml (2 doses from applicator) per calf should be administered orally:

• As soon as possible after birth

• To bought-in calves on arrival at the farm

• At times of stress, as necessary.

For the following two days, 2.5ml / head (1 dose) should be administered before the morning feed.

One dose is administered by each stroke of the pump through the short dispensing nozzle of the dose dispenser into the calf’s mouth.

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Contraindications

Do not use while administrating therapeutic or in-feed antibiotics.

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Adverse reactions

None reported.

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Warnings

Special precautions for use in animals

None.

Special precautions to be taken by the person administering the veterinary medicinal product to the animals

Wash hands after use.

Avoid contact with eyes.

If eye contact occurs, rinse eye with clean, fresh water immediately.

If irritation occurs seek medical advice.

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Use during pregnancy, lactation or lay

Not relevant. Only for use in pre-ruminant calves.

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Interactions

Chlortetracycline, oxytetracycline, tetracycline, penicillin, virginiamycin and tylosin have all been shown to be antagonistic to lactic acid bacteria.

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Overdose

None.

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Special warnings

None.

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Withdrawal period

Meat and offal: Zero days

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Incompatibilities

None known.

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Immediate packaging

White, opaque, high density polyethylene (HDPE) 100ml bottle with a white opaque, screw fit HDPE cap. Contents administrated via a HDPE metered dose pump contained within the cap, delivering 2.5ml.

Available in cartons of 1 x 100ml

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Storage

Store in a refrigerator (2⁰C - 8⁰ C)

Protect from light.

Do not freeze.

Discard unused material.

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Shelf life

Shelf life of the veterinary medicinal product as packaged for sale: 18 months. Shelf life after first opening the immediate packaging: 3 months.

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Disposal of unused product

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.

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Additional information

9 DATE OF FIRST AUTHORISATION

20 December 1995

10 DATE OF REVISION OF THE TEXT

May 2025

Approved 10 June 2025

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Registration holder

For IE only

Provita Eurotech Ireland Ltd, 13/18 City Quay, Dublin 2, Ireland D02 ED70

For UK only

Provita Eurotech Limited, 21 Bankmore Road, Omagh, Co.Tyrone, BT79 0EU, Northern Ireland.

Telephone: +44 (0)28 8225 2352

Fax: +44 (0)28 82241734

E: [email protected]

MANUFACTURER RESPONSIBLE FOR BATCH RELEASE FOR IE and UK:

Provita Eurotech Ltd, 21 Bankmore Road, Omagh, Co.Tyrone, BT79 0EU, Northern Ireland

Telephone +44 (0)28 8225 2352

Fax: +44 (0) 2882241734

E: [email protected]

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