Neocell

TYLOSIN / ANAFASIS Water soluble powder

STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENTS per gr
Active substance:
Tylosin  tartrate ……………………………………………………….. 1000 mg

TARGET SPECIES
Broilers, hens, turkeys.

INDICATION(S)
For the treatment of infections caused by Mycoplasma synoviae in broilers, hens and chickens and Mycoplasma gallisepticum S6 in hens, chickens and turkeys. In practice Tylosin tartrate contributes in the reduction of infections from the stress caused by vaccinations.

DOSAGE FOR EACH SPECIES
Treatment of Mycoplasmosis
Broilers                                             24-72 hours    0,5 gr Tylosin 100%/l of water
Replacement hens and laying hens     48-72 hours    0,5 gr Tylosin 100%/l of water
Turkeys                                            48-120 hours   0,5 gr Tylosin 100%/l of water

ROUTE(S) AND METHOD OF ADMINISTRATION
Oral administration

ADVICE ON CORRECT ADMINISTRATION
It should be administrated in the recommended doses exclusively after dissolution in potable water

CONTRAINDICATIONS
They are not reported for the species which the product is indicated.

ADVERSE REACTIONS
Are not reported
< If you observe any adverse reaction you are kindly requested to inform your veterinarian. >

WITHDRAWAL PERIOD
The animals should not be slaughtered during treatment.
Meat            
Broilers, Hens:        1 day                     
Turkeys:               5 days  
Eggs             
Hens:                  0 days

SPECIAL STORAGE PRECAUTIONS
To be kept in place, which can’t be seen or approached by the children
After its dissolution in potable water it remains constant for 3 days.
After the first opening the product should be used in 20 days.
The shelf life of the product is 24 months from the date of production if it is maintained in closed packing in temperature of environment (≤ 25^ο C).

SPECIAL WARNING(S)
The direct contact with the product must be avoided. It is likely to be observed contact dermatitis.  

SPECIAL PRECAUTIONS FOR THE DISPOSAL OF UNUSED PRODUCT OR WASTE MATERIALS, IF ANY
Each not used veterinary pharmaceutical product or unused remains should be rejected according to the being in effect national requirements.