OSMONDS DRY COW INTRAMAMMARY SUSPENSION

Country: Ireland

Language: English

Source: HPRA (Health Products Regulatory Authority)

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Active ingredient:

NEOMYCIN SULPHATE PH. EUR., PENETHAMATE HYDRIODIDE, PROCAINE BENZYLPENICILLIN

Available from:

Cross Vetpharm Group Limited

ATC code:

QJ51RC

INN (International Name):

NEOMYCIN SULPHATE PH. EUR., PENETHAMATE HYDRIODIDE, PROCAINE BENZYLPENICILLIN

Dosage:

Unknown

Pharmaceutical form:

intramammary Suspension

Prescription type:

POM

Therapeutic group:

Bovine

Therapeutic area:

Beta-lactam antibacterials, penicillins, combinations with other antibacterials

Therapeutic indications:

Antibacterial

Authorization status:

Authorised

Authorization date:

1987-10-01

Summary of Product characteristics

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Osmonds Dry Cow Intramammary Suspension
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Intramammary suspension
A smooth, off white, oily suspension.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cows.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For routine use in cows at drying off, to treat existing intramammary infections and to assist in preventing new
infections occurring during the dry period.
4.3 CONTRAINDICATIONS
Do not use in lactating cows.
Do not use within 50 days prior to calving.
Do not use in animals with known hypersensitivity to the active ingredients.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
Each 4.5 g syringe contains:
ACTIVE SUBSTANCE(S):
Neomycin sulphate
100 mg
Penethamate hydriodide
100 mg
Procaine benzylpenicillin
400 mg
For a full list of excipients, see section 6.1
HEALTH PRODUCTS REGULATORY AUTHORITY
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_Date Printed 13/11/2015_
_CRN 7021877_
_page number: 1_
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTION(S) FOR USE IN ANIMALS
None.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE VETERINARY MEDICINAL PRODUCT TO ANIMALS
Operators should avoid contact with this preparation as occasionally skin allergy may occur.
Penicillins and cephalosporins may cause sensitisation following injection, inhalation, ingestion or skin contact. Sensitivity
to penicillins may lead to cross sensitivity to cephalosporins and vice versa. Allergic reactions to these substances may
occasionally be serious.
Do not handle this product if you know that you are sensitised or if you have been advised not to work with such
preparations.
If you develop symptoms such as skin 
                                
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