AUROFAC D DISPERSIBLE ANTIBIOTIC FEED SUPPLEMENT

Country: Australia

Language: English

Source: APVMA (Australian Pesticides and Veterinary Medicines Authority)

Active ingredient:

CHLORTETRACYCLINE HYDROCHLORIDE

Available from:

BEC FEED SOLUTIONS PTY LTD

INN (International Name):

chlortetracycline HCl(10g/kg)

Pharmaceutical form:

ORAL POWDER, PRE-MIX

Composition:

CHLORTETRACYCLINE HYDROCHLORIDE ANTIBIOTIC Active 10.0 g/kg

Units in package:

5kg

Class:

VM - Veterinary Medicine

Manufactured by:

BEC FEED SOLUTIONS

Therapeutic group:

CALF | PIG - PIGLET | BEEF CALF | BOVINE | CALF - PODDY | CALF - PREWEANING | CALF - SUCKER | DAIRY CALF | NEONATAL CALF | NEONA

Therapeutic area:

NUTRITION & METABOLISM

Therapeutic indications:

BACTERIA SENSITIVE TO CHLORTETRACYCLINE

Product summary:

Poison schedule: 4; Withholding period: WITHHOLDING PERIOD: MEAT (CATTLE): REM OVE ALL MEDICATED FEED 10 DAYS BEFORE SLAUGHTER FOR HUMAN CONSUMPTION. MEAT (PIGS): REMOVE ALL MEDICATED FEED 7 D AYS BEFORE SLAUGHTER FOR HUMAN CONSUMP TION. MILK: DO NOT FEED TO COWS WHICH A RE PRODUCING OR MAY IN THE FUTURE PROD UCE MILK THAT MAY BE USED OR PROCESSED FOR HUMAN CONSUMPTION. TRADE ADVICE: EXPORT SLAUGHTER INTERVAL (ESI): THIS PRODUCT DOES NOT HAVE AN ESI ESTABLIS HED. FOR ADVICE ON THE ESI CONTACT BE C FEED SOLUTIONS PTY LTD ON 1300 884 5 93 BEFORE USING THIS PRODUCT.; Host/pest details: CALF: [BACTERIA SENSITIVE TO CHLORTETRACYCLINE]; PIG - PIGLET: [BACTERIA SENSITIVE TO CHLORTETRACYCLINE]; Poison schedule: 4; Withholding period: ; Host/pest details: CALF: [BACTERIA SENSITIVE TO CHLORTETRACYCLINE]; PIG - PIGLET: [BACTERIA SENSITIVE TO CHLORTETRACYCLINE]; For the prevention of diseases in pigs and calves caused by bacteria sensitive to chlortetracycline.DO NOT FEED to cows which are producing or may in the future produce milk that may be used or processed for human consumption.

Authorization status:

Stopped

Authorization date:

2023-07-01

Patient Information leaflet

AUROFAC® D
DISP
E
RSIBLE
ANTIB
I OT
IC
F
EED
SUPPLEMENT
DIRECTIONS FOR USE:
AUROFAC®
Dis
recommended for addition
to
liquid milk replacer feed of
calves. For young calves
on
liquid feed, each
500
g
of
dry milk
replacer
fortified with 5 g
of
AUROFAC® D
can
be
made
up
to
5 litres by the
addition
of
lukewarm water.
It
may also be mixed with dry feed for pigs
and
calves.
PIGS
UP
TO 12 WEEKS
OF
AGE
Thoroughly
mi
x 10
kg
AUROFAC® D Dispersible Antibiotic
Feed
Supplement with each
tonn
~
of
starter feed.
CALVES UP TO 12 WEEKS
OF
AGE
Thoroughly
mi
x 5 g AUROFAC® D Dispersible Antibiotic Feed
Supplement with each 500 g
of
dry
feed
.
RESTRAINTS
DO
NOT FEED to cows which
are
producing or may
in
the future produce
milk that may
be
used or processed for human consumption.
CONTRAINDICATIONS
This product
is
contraindicated for use
in
ruminating animals.
(
9 I
)
05
00(
I 0 )
2985
3
WITHHOLDING PERIOD:
MEAT (CATTLE):
REMOVE
ALL
MEDICATED FEED 10 days before
slaughter
for
human
consumption
.
MEAT (PIGS):
REMOVE
ALL
MEDICATED
FEED
7 days
before
slaughter
for
human
consumption
.
MILK:
DO
NOT FEED
to
cows
which
are
producing
or
may in the
future
produce milk
that
may be used
or
processed
for
human con-
sumption.
TRADE ADVICE:
EXPORT SLAUGHTER INTERVAL (ESI): This
product does not have
an
ESI
established.
For advice
on
the
ESI
, con-
tact BEC Feed Solutions Ply
Ltd
on
1300 884
593
before using this prod-
uct.
FIRST AID:
If
poi
soning occurs, contact a Doctor or Poisons Information
Centre.
Ph
. Australia 131126, New Zealand 0800
764
766.
DISPOSAL:
For plastic containers
and
bag
liners, triple or (preferably) pressure rinse
into
th
e medicated feed .
Do
not dispose
of
undiluted chemicals
on
-site.
Puncture
or
shred
and
bury empty containers or bag liners in a local
authority landfill.
If
no
landfill available, bury the containers below 500
mm
in
a disposal pit specifically marked
and
set
up
for this purpose clear
of
waterways, vegetation
and
roots.
Empty
containers
and
product
should not
be
burnt. If recyclable, return clean contai

Summary of Product characteristics

_MATERIAL SAFETY DATA SHEET _
_ _
_ _
_ _
ADISSEO AUSTRALIA PTY LIMITED
ABN 54 098 527 247
_AUROFAC D™ _
Page 1 of total 3
Date of Issue: Feb 2005
NOT CLASSIFIED AS HAZARDOUS ACCORDING TO CRITERIA OF WORKSAFE
AUSTRALIA
COMPANY:
Adisseo Australia Pty Limited
ADDRESS:
66 Antimony St CAROLE PARK QLD 4300
TELEPHONE:
[phone]
FAX:
[phone]
EMERGENCY TELEPHONE:
[phone] (office hours)
IDENTIFICATION
PRODUCT NAME:
AUROFAC D™
OTHER NAMES:
Chlortetracycline 1% soluble premix
MANUFACTURER’S PRODUCT CODE: 84002100
UN NUMBER:
None allocated
DANGEROUS GOODS CLASS:
None allocated
SUBSIDIARY RISK:
None allocated
HAZCHEM CODE:
None allocated
POISONS SCHEDULE NUMBER:
4
USE:
Water dispersible medication for calves, pigs and
poultry.
PHYSICAL DESCRIPTION/PROPERTIES
APPEARANCE:
White free flowing powder
BOILING POINT/MELTING POINT:
Not available
VAPOUR PRESSURE:
Not relevant
SPECIFIC GRAVITY:
Not available
FLASHPOINT:
Not available
FLAMMABILITY LIMITS:
May form an explosive dust cloud
SOLUBILITY IN WATER:
Soluble
OTHER PROPERTIES
PH
Not available
BULK DENSITY
Not available
INGREDIENTS
_CHEMICAL NAME _
_CAS NUMBER _
_PROPORTION_
Ingredients determined not to
be hazardous
Not relevant
to 100%
Chlortetracycline
57-65-2
1.2%
msds84002100- Aurofac DT.doc
_MATERIAL SAFETY DATA SHEET _
_ _
_ _
_ _
ADISSEO AUSTRALIA PTY LIMITED
ABN 54 098 527 247
_AUROFAC D™ _
Page 2 of total 3
Date of Issue: Feb 2005
HEALTH HAZARD INFORMATION
HEALTH EFFECTS
The oral LD
50
for rats for pure Chlortetracycline is >3000
mg/kg. This is equivalent to >250 000 mg/kg of this
compound which means it is not classified as hazardous.
Exposure to high levels of Chlortetracycline may cause
mucous
membrane
irritation
(inflammation),
hepatic
system
effects
(elevated
liver
enzyme
levels
and
jaundice),
gastrointestinal
effects
(nausea,
vomiting,
diarrhoea, constipation, cramps and loss of appetite),
renal
system
effects
(urine
retention,
changed
urine
production, painful urination, blood in urine).
Inhalation of high levels of Chlortetracycline may