SELENIUM ORAL CONCENTRATE

Country: Australia

Language: English

Source: APVMA (Australian Pesticides and Veterinary Medicines Authority)

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Active ingredient:

SELENIUM AS SODIUM SELENITE

Available from:

NUTRIEN AG SOLUTIONS LIMITED

INN (International Name):

Se as sod.selenite(10mg/mL)

Pharmaceutical form:

TOPICAL SOLUTION/SUSPENSION

Composition:

SELENIUM AS SODIUM SELENITE MINERAL-SELENIUM Active 10.0 mg/ml

Units in package:

5L

Class:

VM - Veterinary Medicine

Manufactured by:

LANDMARK OPERATIONS

Therapeutic area:

NUTRITION & METABOLISM

Product summary:

Poison schedule: 7; Withholding period: WITHHOLDING PERIODS: Zero (0) days. TRADE ADVICE EXPORT SLAUGHTER INTERVAL (ESI): Zero (0) days.; Host/pest details: CATTLE: [SELENIUM DEFICIENCY, WHITE MUSCLE DISEASE]; POULTRY: [SELENIUM DEFICIENCY, WHITE MUSCLE DISEASE]; SHEEP: [SELENIUM DEFICIENCY, WHITE MUSCLE DISEASE]; Poison schedule: 7; Withholding period: ; Host/pest details: CATTLE: [SELENIUM DEFICIENCY, WHITE MUSCLE DISEASE]; POULTRY: [SELENIUM DEFICIENCY, WHITE MUSCLE DISEASE]; SHEEP: [SELENIUM DEFICIENCY, WHITE MUSCLE DISEASE]; For the prevention and treatment of white muscle disease, (W.M.D) and other conditions caused by selenium deficiency in sheep, cattle and poultry.See CONTRAINDICATIONS section on label. A veterinarian should establish that a selenium problem exists before treatment is initiated. Not compatible with products containing copper sulphate.

Authorization status:

Registered

Authorization date:

2023-07-01

Patient Information leaflet

                                ~~~~~~~~
~~~~~~~~~~~~~--~~~~~~~~~~~~~~~~~~~~··----"·-
TEMPLATE FOR RELEVANT LABEL PARTICULARS (RLPS)
(VETERINARY PRODUCTS)
Select appropriate:
!Rl
New Product (include all applicable RLPs)
OR
RLP
Approved
D
Variation (highlight instructions that are being varied). Approval no.
of
label being varied:
Signal
heading:
DANGEROUS POISON
KEEP OUT OF REACH OF CHILDREN
READ SAFETY DIRECTIONS BEFORE OPENING OR USING
FOR ANIMAL TREATMENT ONLY
PRODUCT
NAME:
SELENIUM ORAL CONCENTRATE
Active
ACTIVE CONSTITUENT: 10
MG
SELENIUM
(Se)
PER ML
AS
SODIUM SELENITE
CONSTITUENTLS:
Statement
of
FOR THE PREVENTION AND TREATMENT OF WHITE MUSCLE DISEASE
claims:
(W.M.D.) AND OTHER CONDITIONS CAUSED BY SELENIUM DEFICIENCY
IN
SHEEP, CATTLE AND POULTRY.
Net
contents:
5L
DIRECTIONS
FOR
USE
DIRECTIONS FOR USE:
Heading:
Restraints:
CONTRAINDICATIONS:
CONTRAINDICATIONS:
This product
is
contraindicated for use when selenium intake from pasture
is
high
or selenium
is
provided by other means (such as top dressing, vaccine, pellets or
selenium drenches) if blood selenium levels at treatment are high.
Users can
determine selenium status by consulting their veterinarian.
This product
is
contraindicated for use in animals that are dehydrated or unwell.
PRECAUTIONS:
PRECAUTIONS:
Minerals such as copper, cobalt, selenium, iron, manganese and
molybdenum
compete with each other for metabolically important processes
in
the animal.
Users should seek veterinary advice before treatment.
Side
effects:
Dosage
&
DOSAGE AND ADMINISTATION:
ADMINISTRATION:
TO MAKE UP DRENCH.
Dilute Selenium Concentrate
as
follows:
Mix one part
Selenium Concentrate with 9 parts water (e.g.
50
ml
Selenium Concentrate with
450
ml
of water).
Administer 1
ml
of diluted product/1 0
kg
bodyweight for sheep and cattle using
any standard drenching equipment. Check dose rates and equipment
before
drenching commences. Then dose as follows:
APPLICATION
AMOUNT OF DILUTED SELENIUM
DRENCH PER ANIMAL
EWES:
For congenital W.M.D.
in
lambs dose one
month before mating and one month
5
ml
before
lam
bi
                                
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