IDYNE

Main information

  • Trade name:
  • IDYNE IODOPHOR DAIRY SANITISER
  • Pharmaceutical form:
  • LIQUID CONCENTRATE
  • Units in package:
  • 5L,20L,25L,110L,200L
  • Class:
  • AgChem
  • Medicine domain:
  • Equipment
  • Medicine type:
  • Agrochemical

Documents

Localization

  • Available in:
  • IDYNE IODOPHOR DAIRY SANITISER
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • MILKING EQUIPMENT | MILKING MACHINE
  • Therapeutic area:
  • dairy cleanser
  • Therapeutic indications:
  • MILKSTONE REMOVAL | MILK FAT | MILK PROTEIN | MINERAL DEPOSITS
  • Product summary:
  • An iodine based pre-milking sanitiser which is used to sanitise milking machine.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 30112/0601
  • Authorization date:
  • 15-06-2001
  • Last update:
  • 15-06-2017

Patient Information leaflet: composition, indications, side effects, dosage, interactions, adverse reactions, pregnancy, lactation

Issue No 2

Page 1 of 3

Issue Date : 01/05/2001

DRAFT LABEL OF

IDYNE

IODOPHOR DAIRY SANITISER

Front Label

POISON

KEEP OUT OF REACH OF CHILDREN

READ SAFETY DIRECTIONS BEFORE OPENING OR USING

IDYNE

IODOPHOR DAIRY SANITISER

ACTIVE CONSTITUENT: 160 g/L PHOSPHORIC ACID

g/L SULPHAMIC ACID

20 g/L IODINE

LOW FOAMING DETERGENT FOR MILKSTONE REMOVAL IN MILKING

PLANTS

CONTENTS: 5L, 20L ( 25L, 110L, 200L)

Info

pest

Verified

Issue No 2

Page 2 of 3

Issue Date : 01/05/2001

APPLICATION :

IDYNE IODPOPHOR DAIRY SANITISER is an iodine based pre milking sanitiser

which is used to sanitise milking machine equipment.

DIRECTIONS FOR USE: (ALL STATES )

SITUATION PURPOSE: RATE:

CRITICAL

COMMENTS:

Use after morning

milking

1. WARM IDYNE

Milking Plant

Sanitising of Standard solution SOLUTION

milking

16 mL per 10L of

Flush plant a standard

machine

hot water

solution using 5L per

equipment

(less than 50 deg C ) set of cups

2. DRAIN

Allow milking machine to

Drain for at least 5 minutes

3. HOT RINSE

Rinse plant with boiling

water using 5L per set of

cups

NOT TO BE USED FOR ANY PURPOSE OR IN ANY MANNER CONTRARY

TO THIS LABEL UNLESS AUTHORISED UNDER APPROPRIATE

LEGISLATION

PROTECTION OF WILDLIFE, FISH, CRUSTACEA AND ENVIRONMENT :

Dangerous to fish. Do not contaminate streams, rivers or waterways with the chemical

or used containers.

STORAGE AND DISPOSAL:

Store in closed, original container in a well ventilated area, as cool as possible, out of

direct sunlight. Triple or preferably pressure rinse containers before disposal. Add

rinsings to solution. Do not dispose of undiluted chemicals on site. If recycling,

replace cap and return clean container to recycler or point of supply. If not recycling,

break, crush, or puncture and bury empty containers in a local authority landfill. If

there is no local authority landfill readily available in your area, bury the containers at

a depth of 500mm in a disposal pit specifically marked and set up for this purpose

clear of waterways, desirable vegetation and tree roots. Empty containers and product

should not be burnt.

Issue No 2

Page 3 of 3

Issue Date : 01/05/2001

SAFETY DIRECTIONS :

Corrosive. Attacks eyes, nose, throat and skin. Avoid contact with eyes, skin and

clothing. Do not inhale vapour or spray mist. When preparing the product for

use wear cotton overalls buttoned to the neck and wrists, a washable hat, rubber

apron, elbow length neoprene gloves, a face shield and chemical resistance

footwear. If clothing becomes contaminated with the product remove clothing

immediately. If product on skin immediately wash area with soap and water. If

product in eyes wash it out immediately with water. After use and before eating,

drinking or smoking wash hands, arms and face with soap and water. After each

day’s use wash gloves, face shield and contaminated clothing.

FIRST AID :

If poisoning occurs, contact a Doctor or Poisons Information Centre. ( eg Australia

13 1126). If swallowed do NOT induce vomiting. Give a glass of water. If skin

contact occurs, remove contaminated clothing and wash skin thoroughly. If in eyes,

hold eyes open, flood with water for at least 15 minutes and see a Doctor. For further

information refer to the MSDS for the product.

NRA Approval No: 30112/0601

Batch No:

Date of Manufacture :

UN 1805 HAZCHEM 2R CLASS 8 P.G. III

In a transport emergency dial 000, police or fire brigade

Manufactured by:

Tasman Chemicals Pty Ltd

2 – 6 Roberna Street

Moorabbin

Victoria 3189

Phone: (03) 9555 8033

Fax:

(03) 9553 2902

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13-12-2018

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7-12-2018

Re‐evaluation of propane‐1,2‐diol esters of fatty acids (E 477) as a food additive

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Published on: Thu, 06 Dec 2018 The EFSA Panel on Food Additives and Flavourings (FAF) provides a scientific opinion re‐evaluating the safety of propane‐1,2‐diol esters of fatty acids (E 477) when used as a food additive. The Scientific Committee on Food (SCF) in 1978 endorsed the acceptable daily intake (ADI) of 25 mg/kg body weight (bw) per day, expressed as propane‐1,2‐diol, established by the Joint FAO/WHO Expert Committee on Food Additives (JECFA) in 1974. No adverse effects were observed in short‐t...

Europe - EFSA - European Food Safety Authority Publications

1-12-2018

Safety evaluation of the food enzyme endo‐1,4‐β‐xylanase from a genetically modified Trichoderma reesei (strain DP‐Nzd22)

Safety evaluation of the food enzyme endo‐1,4‐β‐xylanase from a genetically modified Trichoderma reesei (strain DP‐Nzd22)

Published on: Fri, 30 Nov 2018 The food enzyme endo‐1,4‐β‐xylanase (EC 3.2.1.8) is produced with a genetically modified Trichoderma reesei (strain DP‐Nzd22) by DuPont. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. The endo‐1,4‐β‐xylanase is intended to be used in distilled alcohol production, bakery and brewery. Residual amounts of total organic solids (TOS) are removed during the production of dis...

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21-11-2018

Risk for animal and human health related to the presence of dioxins and dioxin-like PCBs in feed and food

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19-11-2018

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FDA issues a qualified health claim for oleic acid oils based on data showing it reduces cholesterols levels.

FDA - U.S. Food and Drug Administration

9-11-2018

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31-10-2018

Safety and efficacy of a super critical carbon dioxide extract of Humulus lupulus L. flos when used as a feed flavouring for all animal species

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Published on: Tue, 30 Oct 2018 00:00:00 +0100 Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of a super critical carbon dioxide extract of Humulus lupulus L. flos (hop strobiles) when used as a sensory feed additive for all animal species. The additive is specified to containing 40% beta acids and less than 0.2% alpha acids. Known substances of conce...

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11-10-2018

Re‐evaluation of oxidised soya bean oil interacted with mono‐ and diglycerides of fatty acids (E 479b) as a food additive

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22-9-2018

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22-9-2018

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9-4-2010

Consultation responses on the Reimbursement Committee’s recommendation concerning the reimbursement status of medicinal products in ATC group A02 (drugs for acid related disorders)

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17-12-2009

Consultation on the Reimbursement Committee's recommendation concerning the reimbursement status of medicinal products in ATC group A02 (drugs for acid related disorders)

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Opinion/decision on a Paediatric investigation plan (PIP): Recombinant human acid ceramidase (RVT-801), decision type: , therapeutic area: , PIP number: P/0319/2018

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Europe - EMA - European Medicines Agency

19-12-2018


Orphan designation: (S)-(−)-3-(4-aminophenyl)-2-methoxypropanoic acid, Treatment of idiopathic pulmonary fibrosis, 24/08/2018, Positive

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18-12-2018


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18-12-2018


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12-12-2018


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30-11-2018

Keppra (UCB Pharma S.A.)

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Keppra (Active substance: levetiracetam) - Centralised - Yearly update - Commission Decision (2018)8160 of Fri, 30 Nov 2018

Europe -DG Health and Food Safety

26-11-2018


Withdrawn application: HopGuard Gold, purified semi-solid extract from Humulus lupulus L. containing approximately 48% of beta acids as potassium salts, Date of withdrawal: 12/04/2018, Initial authorisation

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Europe - EMA - European Medicines Agency

22-11-2018


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Europe - EMA - European Medicines Agency

22-11-2018


Opinion/decision on a Paediatric investigation plan (PIP): Citric acid (as citric acid anhydrous) / sodium chloride / simeticone / macrogol 4000 / sodium citrate /sodium sulfate (as sodium sulfate anhydrous) / potassium chloride (PMF104), decision type:

Opinion/decision on a Paediatric investigation plan (PIP): Citric acid (as citric acid anhydrous) / sodium chloride / simeticone / macrogol 4000 / sodium citrate /sodium sulfate (as sodium sulfate anhydrous) / potassium chloride (PMF104), decision type:

Opinion/decision on a Paediatric investigation plan (PIP): Citric acid (as citric acid anhydrous) / sodium chloride / simeticone / macrogol 4000 / sodium citrate /sodium sulfate (as sodium sulfate anhydrous) / potassium chloride (PMF104), decision type: , therapeutic area: , PIP number: P/0223/2018

Europe - EMA - European Medicines Agency

30-10-2018

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Active substance: Glycine, L-alanine, L-arginine, L-aspartic acid, L-cysteine, L-cystine, L-glutamic acid, L-histidine, L-lysine monohydrate, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, taurine) - Orphan designation - Commission Decision (2018)7277 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/100/18

Europe -DG Health and Food Safety

29-10-2018

Clopidogrel/Acetylsalicylic acid Zentiva (Sanofi-Aventis groupe)

Clopidogrel/Acetylsalicylic acid Zentiva (Sanofi-Aventis groupe)

Clopidogrel/Acetylsalicylic acid Zentiva (Active substance: clopidogrel / acetylsalicylic acid) - Centralised - 2-Monthly update - Commission Decision (2018)7249 of Mon, 29 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1144/WS1433/0051

Europe -DG Health and Food Safety

2-10-2018

Zoledronic acid Actavis (Actavis Group PTC ehf.)

Zoledronic acid Actavis (Actavis Group PTC ehf.)

Zoledronic acid Actavis (Active substance: zoledronic acid) - Centralised - Yearly update - Commission Decision (2018)6488 of Tue, 02 Oct 2018

Europe -DG Health and Food Safety

2-10-2018

Zoledronic acid Mylan (Mylan S.A.S.)

Zoledronic acid Mylan (Mylan S.A.S.)

Zoledronic acid Mylan (Active substance: zoledronic acid) - Centralised - Yearly update - Commission Decision (2018)6486 of Tue, 02 Oct 2018

Europe -DG Health and Food Safety

2-10-2018

Zoledronic acid Teva (Teva B.V.)

Zoledronic acid Teva (Teva B.V.)

Zoledronic acid Teva (Active substance: zoledronic acid) - Centralised - Yearly update - Commission Decision (2018)6466 of Tue, 02 Oct 2018

Europe -DG Health and Food Safety

24-9-2018

Zoledronic acid Hospira (Pfizer Europe MA EEIG)

Zoledronic acid Hospira (Pfizer Europe MA EEIG)

Zoledronic acid Hospira (Active substance: zoledronic acid) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6243 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2365/T/33

Europe -DG Health and Food Safety

6-8-2018

Zoledronic acid Accord (Accord Healthcare Limited)

Zoledronic acid Accord (Accord Healthcare Limited)

Zoledronic acid Accord (Active substance: zoledronic acid) - Centralised - Yearly update - Commission Decision (2018)5386 of Mon, 06 Aug 2018

Europe -DG Health and Food Safety

30-7-2018

Esmya (Gedeon Richter Plc.)

Esmya (Gedeon Richter Plc.)

Esmya (Active substance: ulipristal) - Referral - Commission Decision (2018)5101 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2041/A-20

Europe -DG Health and Food Safety

11-7-2018

Vantavo (Merck Sharp and Dohme B.V.)

Vantavo (Merck Sharp and Dohme B.V.)

Vantavo (Active substance: alendronic acid / colecalciferol) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4511 of Wed, 11 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1180/T/30

Europe -DG Health and Food Safety

4-6-2018

Chenodeoxycholic acid Leadiant (Leadiant GmbH)

Chenodeoxycholic acid Leadiant (Leadiant GmbH)

Chenodeoxycholic acid Leadiant (Active substance: chenodeoxycholic acid) - Centralised - Yearly update - Commission Decision (2018)3627 of Mon, 04 Jun 2018

Europe -DG Health and Food Safety

8-3-2018

Mycophenolate mofetil, mycophenolic acid

Mycophenolate mofetil, mycophenolic acid

Mycophenolate mofetil, mycophenolic acid (Active substance: mycophenolate mofetil or mycophenolic acid) - Centralised - Art 28 - (PSUR - Commission Decision (2018)1540 of Thu, 08 Mar 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10550/201705

Europe -DG Health and Food Safety