POM-V Prescription Required

Ubrostar Red 100 mg / 280 mg / 100 mg, Intramammary Suspension for Cattle

Active ingredients: Benethamine Penicillin, Framycetin Sulphate, Penethamate hydriodide, non-micronised

Form

Intramammary

Species

Cattle

Manufacturer

Boehringer Ingelheim Vetmedica GmbH

VMD MA No.

04491/3031

View official SPC (PDF)

The prescription itself has a price. See what practices near you charge for a consultation and the written prescription fee.

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1

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Prescription required

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Clinical information

Ubrostar Red 100 mg / 280 mg / 100 mg, Intramammary Suspension for Cattle — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

Intramammary administration of 100 mg penethamate hydriodide, 280 mg
benethamine penicillin and 100 mg framycetin sulphate into each quarter, i.e. the
contents of one syringe to be infused into each quarter immediately after the last
milking of a lactation.
Before infusion, the udder should be milked out completely, the teats should be
thoroughly cleaned and disinfected, and care should be taken to avoid contamination
of the injector nozzle. Following infusion, it is advisable to use a teat wipe or spray.

Do not use in lactating cows.
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.

Cattle (Cows at drying off):
None known.
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or its local representative or the national
competent authority via the national reporting system. See the package leaflet for
respective contact details.

Where there is a risk of summer mastitis, additional management procedures, such
as fly control should be considered.

Special precautions for safe use in the target species:
Use of the veterinary medicinal product should be based on susceptibility testing of
the bacteria isolated from the animal.
If this is not possible, therapy should be based on local (regional, farm level)
epidemiological information about susceptibility of the target bacteria. Official and
local antimicrobial policies should be taken into account when the veterinary
medicinal product is used.
Serious acute mastitis [potentially lethal] due to pathogens like Pseudomonas
aeruginosa, can occur after drying off despite preventive treatment. Good aseptic
practices should be thoroughly respected in order to reduce that risk; cows should be
housed in a hygienic paddock far from the milking parlour and regularly checked
several days after drying off.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Skin sensitisation may occur in persons handling the veterinary medicinal product;
care should be taken to avoid contact with skin.
Penicillins and cephalosporins may cause hypersensitivity following injection,
inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross
reactions to cephalosporins and vice versa. Allergic reactions to these substances
may occasionally be serious.
1. Do not handle the veterinary medicinal product if you know that you are
sensitised, or if you have been advised not to work with such preparations.
2. Handle this veterinary medicinal product with care (especially persons with skin
damage) to avoid exposure. Wear gloves, wash hands in case of contact with
skin.
3. If you develop symptoms such as a skin rash following exposure, seek medical
advice and show the package leaflet or the label to the physician. Swelling of the
face, lips or eyes, or difficulty breathing are more serious symptoms and require
urgent medical attention.
Special precautions for the protection of the environment:
Not applicable.

None known.

Do not store above 25 C.

Meat and offal: 10 days.
Milk: If treated at least 35 days before calving, milk must not be used for 36 hours
after calving.
If treated less than 35 days before calving, milk must not be used for 37 days
after treatment.
4.

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.