Bovaclox DC Xtra Intramammary Suspension is a dry cow tube containing cloxacillin and ampicillin in a long acting base.
It is active against both Gram-positive and Gram negative organisms associated with mastitis and is effective against Streptococcus agalactiae and other Streptococcus species, penicillin resistant and sensitive Staphylococci, Corynebacterium species, Arcanobacteria species, Escherichia coli and other susceptible Gram-negative bacteria.
Active Ingredients: Cloxacillin 600 mg (as Cloxacillin benzathine) Ampicillin 300 mg (as Ampicillin trihydrate)
Benefits:
- Long-Acting Protection: Maintains effective antibacterial levels in the cow’s udder for up to 10 weeks.
- Broad-Spectrum Efficacy: Targets both Gram-positive and Gram-negative bacteria, including Streptococcus agalactiae, Staphylococci (both penicillin-resistant and sensitive), Corynebacterium, and Escherichia coli.
- Summer Mastitis Prevention: Acts as a useful aid in reducing the incidence of summer mastitis in dry cows and heifers at risk.
- Tissue Friendly: Formulated as a non-irritating oily suspension to protect sensitive udder tissue.
Dosage:
Dry Off Therapy: After the final milking of a lactation, clean and disinfect the teats and introduce the contents of one tube into each quarter via the teat canal.
Avoid contamination of the syringe nozzle. When infusing heifers it is important that the syringe nozzle is not introduced into the teat.
The recommended procedure is as follows: The animal(s) should be properly restrained. The teats are cleaned and disinfected.
The teat orifice is located and the nozzle of the syringe placed against it but NOT inserted. When the syringe plunger is depressed the antibiotic passes easily through the teat into the udder.
Milk Withdrawal: Do not use in lactating cows. Milk must not be used for human consumption for a designated period post-calving (refer to local product label or prescribing vet, typically around 96 to 156 hours).
Meat Withdrawal: Cattle must not be slaughtered for human consumption during treatment or within 28 days of the last administration.
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