DYSTOSEL EMULSION

Country: Canada

Language: English

Source: Health Canada

Active ingredient:

SELENIUM (SODIUM SELENITE); VITAMIN E (D-ALPHA TOCOPHERYL ACETATE)

Available from:

ZOETIS CANADA INC

ATC code:

QA11JB

Dosage:

3MG; 136UNIT

Pharmaceutical form:

EMULSION

Composition:

SELENIUM (SODIUM SELENITE) 3MG; VITAMIN E (D-ALPHA TOCOPHERYL ACETATE) 136UNIT

Administration route:

INTRAMUSCULAR

Units in package:

100ML

Prescription type:

OTC

Therapeutic group:

CATTLE; SHEEP

Therapeutic area:

VITAMINS WITH MINERALS

Product summary:

Active ingredient group (AIG) number: 0207501001

Authorization status:

APPROVED

Authorization date:

1999-07-06

Patient Information leaflet

PROOF Nº
COMPONENT
PHARMA CODE
PAR
DESCRIPTION
MARKET
SUPPLIER
SUPPLIER Nº
PERIGORD Nº
COLOURS
Canada
Belapharm
DYSTOSEL SSOL 1 MG/ML 100 ML GVIAL 1 EA IFC
PAR-2014-0025959
01
Carton
N/A
BLACK
PROFILE
18:03
TIME:
04 NOV 2014
DATE:
TEXT SIZE
7.5 PT
THE BODY TEXT
ON THIS A/W IS AT:
01/15 FS1692114PAECA
239842
DIMENSIONS
55 x 55 x 102.5 mm
DRAWING NUMBER
BPS-231
PMS WARM RED
VARNISH FREE
PMS 116
Dystosel
®/MD
_VITAMIN E – _
_SELENIUM INJECTION_
_INJECTION DE VITAMINE E_
_ET SÉLÉNIUM_
DIN 00170968
Dystosel
®
_VITAMIN E –_
_SELENIUM INJECTION_
VETERINARY USE ONLY
STERILE AQUEOUS EMULSION
_for sheep and cattle_
WARNINGS:
Treated
animals
must not be slaughtered for use in
food for at least 21 days after the
latest
treatment
with
this
drug.
This product must not be used in
lactating dairy cattle.
_NET 100 ML_
DIN 00170968
Dystosel
MD
_INJECTION DE VITAMINE E_
_ET SÉLÉNIUM_
USAGE VÉTÉRINAIRE SEULEMENT
ÉMULSION AQUEUSE STÉRILE
_pour moutons et bovins_
MISES EN GARDE : Les animaux
traités ne doivent pas être abattus à
des fins alimentaires dans un délai
d’au moins 21 jours après le dernier
traitement avec ce médicament. Ce
produit ne doit pas être utilisé chez
les vaches laitières en lactation.
_NET 100 ML_
Lot
EXP.
MEDICINAL
INGREDIENTS:
Selenium
(as
sodium
selenite),
3 mg/mL and vitamin E (_dl_-
α
-tocopherol acetate), 136 IU/mL
PRESERVATIVE: Benzyl alcohol, 15 mg/mL
INDICATIONS:
For
the
prevention
and
treatment
of
white
muscle disease (nutritional myopathy) in calves and lambs.
DOSAGE
AND
ADMINISTRATION:
Administer
the
following
single doses subcutaneously or intramuscularly:
PREVENTION: _Postnatal_: _Calves_ – 1 mL/45 kg body weight.
_Lambs,_ Newborn – 0.25 mL per animal; 2 to 8 weeks of age
– 0.5
mL
per
animal.
_Prenatal_:
After
a
pregnancy
of
5 months in cows and 3 months in ewes – 1 mL/45 kg body
weight and repeat, if necessary, at no less than 2 week
intervals for a maximum of 4 doses.
TREATMENT: _Calves_: 2 mL/45 kg body weight.
_Lambs_: 0.5 mL per animal.
CAUTIONS:
This
product