DAIRYAID MARK II

Main information

  • Trade name:
  • DAIRYAID MARK II MILKING MACHINE DETERGENT
  • Pharmaceutical form:
  • Soluble
  • Units in package:
  • 5kg,10kg,20kg,25kg,200kg
  • Class:
  • AgChem
  • Medicine domain:
  • Equipment
  • Medicine type:
  • Agrochemical

Documents

Localization

  • Available in:
  • DAIRYAID MARK II MILKING MACHINE DETERGENT
    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:
  • Medium foaming dairy detergent for removal of milkstone in milking plants.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 30166/0601
  • Authorization date:
  • 06-07-2001
  • Last update:
  • 15-06-2017

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

DRAFT LABEL OF

DAIRY

AlD'

MARK

II

MILKING MACHINE DETERGENT

Front

Label

CAUTION

KEEP OUT OF REACH OF CHILDREN

READ SAFETY DIRECTIONS BEFORE OPENING OR USING

DAIRY

MARK

II

MILKING MACHINE DETERGENT

ACTIVE CONSTITUENT

995 glkg

ALKALINE

SALTS

MEDIUM FOAMING DAIRY

DETERGENT

REMOVAL OF MILKSTONE

MILKING

PLANTS

NET CONTENTS: 5kg,

lOkg (20kg,

200kg)

Issue No 2

Issue

Date:

01/05/2001

N.R.A.

APPROVED

LABEL

JTEXT)

~,..,'"

r'"';c'

-·C.·''OOVh·'

Label

.:-::

.....

Date:

.I.QPoI

.

Ignature

~./.L.I

Page 1

DIRECTIONS FOR USE:

(ALL

STATES)

SITUATION

Milking Plant

PURPOSE:

Milkstone

Removal

RATE:

Standard solution

lSg per 10L

hot water

(6S-70

deg C )

CRITICAL

COMMENTS:

COLD RINSE

Rinse plant with cold

water using SL per

cups

ALKALl

DETERGENT

Flush plant with standard

solution using SL per set

cups

RINSE

Rinse plant with boiling

water using SL per set

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,

direct sunlight.

Triple or preferably pressure rinse containers before disposaL Add

rinsings to solution.

Do not dispose

undiluted chemicals on site.

Break,

crush,

puncture and bury empty containers in a local

authority landfill.

there is no local

authority landfill readily available in your area, bury the containers at a depth

SOOmm

in a disposal pit specifically marked

up for this purpose clear

waterways,

desirable vegetation and tree roots.

Empty containers

product should

not be burnt.

SAFETY DIRECTIONS:

This product is strongly alkaline.

Avoid contact with skin

eyes.

Issue

Issue

Date:

01/0SI2001

Page 2

01'6

FIRST

AID:

poisoning occurs,

contact a Doctor or Poisons Information Centre.

( eg Australia

13 1126).

swallowed do NOT induce vomiting.

Give a glass

water.

skin

contact occurs,

remove contaminated clothing and wash skin thoroughly.

in eyes,

hold eyes open,

flood with water for at

leastl

S minutes and see a Doctor.

For further

information refer to the MSDS for the product.

NRA Approval No: 30166

"

C6D

Batch No:

Date

Manufacture:

Manufactured by:

Tasman Chemicals Pty Ltd

6 Robema Street

Moorabbin

Victoria 3189

Phone: (03) 9555 8033

Fax:

(03) 9553 2902

Issue No 2

Issue

Date:

01/05/200

Page 3

DRAFT LABEL OF

DAffiYAID

MARK

n

MILKING MACHINE DETERGENT

Front

Label

CAUTION

KEEP

OUT

OF REACH OF CIDLDREN

READ SAFETY DIRECTIONS BEFORE OPENING OR USING

DAIRYAID

MARK

II

MILKING MACHINE DETERGENT

ACTIVE CONSTITUENT.

J!~~

ALKALINE SALTS

MEDIUM FOAMING ALKALI DAIRY DETERGENT FOR MILKS TONE

REMOVAL

NET CONTENTS: 25kg

Issue

No 2

Issue

Date:

01/05/2001

Page 4

off)

APPLICATION:

DAIRYAID MARK II MILKING MACHINE DETERGENT is a alkali dairy

detergent for use every evening for milkstone removal.

is designed to be used in

conjunction with THERMOKLEEN ACID MILKSTONE REMOVER POWDER

DIRECTIONS FOR USE:

SITUATION

Milking Plant

PURPOSE:

Milkstone

Removal

RATE:

Standard solution

l5gper

hot water

(65-70 deg C )

CRITICAL

COMMENTS:

Use after evening

milking

COLD RINSE

Rinse plant with cold

water using 5L per

cups

2. HOT ALKALI

DETERGENT

Flush plant with standard

solution using 5L per set

cups

3. HOT RINSE

Rinse plant with boiling

water using 5L per set

cups

NOT TO BE USED

FOR

ANY PURPOSE OR IN ANY MANNER CONTRARY

TO THIS LABEL UNLESS AUTlIORlSED 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,

direct sunlight.

Single rinse before disposal.

Add rinsings to solution.

Do not dispose

undiluted chemicals on site. Puncture and bury empty containers in a local

authority landfill.

there is no local authority landfill

readily available in your area,

bury the containers at a depth

500mm in a disposal

pit specifically marked and set

up for this purpose clear

waterways,

desirable vegetation and tree roots. Empty

containers and product

should not be burnt.

SAFETY DIRECTIONS:

This product

is strongly alkaline.

Avoid contact with skin and eyes.

Issue No 2

Issue

Date:

0110512001

Page 5

FIRST

AID:

If poisoning occurs,

contact a Doctor or Poisons Information Centre.

( eg Australia

13 1126).

swallowed do NOT induce vomiting.

Give a glass

water.

Ifskin

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: 30166

/C(;C

Batch No:

Date ofManufacture :

Manufactured by:

Tasman Chemicals Pty Ltd

6 Roberna Street

Moorabbin

Victoria 3189

Phone: (03) 9555 8033

Fax:

(-03)

9553 2902

Issue No 2

Issue

Date:

01/05/2001

Page 6

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Statement on the safety of d‐ribose

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FDA - U.S. Food and Drug Administration

7-12-2018

Accra Super Market Issues Allergy Alert On Undeclared Peanuts In 'Suya Barbecue Seasoning'

Accra Super Market Issues Allergy Alert On Undeclared Peanuts In 'Suya Barbecue Seasoning'

Accra Super Market of Worcester MA, is recalling 0.53 lbs packages of "Suya Barbecue Seasoning" because it may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

7-12-2018

Magnesium citrate malate as a source of magnesium added for nutritional purposes to food supplements

Magnesium citrate malate as a source of magnesium added for nutritional purposes to food supplements

Published on: Thu, 06 Dec 2018 The present scientific opinion deals with the assessment of the bioavailability of magnesium, from the proposed nutrient source, magnesium citrate malate (MgCM), when added for nutritional purposes to food supplements. MgCM is a mixed salt consisting of magnesium cations and citrate and malate anions, and with a magnesium content of 12–15%. MgCM is proposed to be used in food supplements that are intended to provide up to 300–540 mg/day magnesium. The data provided demonst...

Europe - EFSA - European Food Safety Authority Publications

7-12-2018

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

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

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

6-12-2018

King Soopers and City Market Recalls Abound Chicken and Brown Rice Dog Food Because of Elevated Vitamin D Levels

King Soopers and City Market Recalls Abound Chicken and Brown Rice Dog Food Because of Elevated Vitamin D Levels

Following a recall by Sunshine Mills, Inc., King Soopers announced it has removed from sale Abound Chicken & Brown Rice Recipe dog food produced by Sunshine Mills, Inc. sold in King Soopers and City Market stores, located in Colorado, Utah, New Mexico and Wyoming. Only Abound Chicken & Brown Rice Recipe dog food with the listed UPC numbers and Best by Dates are affected by this recall. The recall was initiated because the product had the potential to contain an elevated level of Vitamin D, which may caus...

FDA - U.S. Food and Drug Administration

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...

Europe - EFSA - European Food Safety Authority Publications

29-11-2018

Glyphosate: ANSES launches a comparative assessment with the available alternatives

Glyphosate: ANSES launches a comparative assessment with the available alternatives

Following the five-year re-approval of this active substance at European level in December 2017, ANSES is reassessing marketing authorisations for products containing glyphosate. For products for which an application for authorisation or re-authorisation has been submitted, the Agency will carry out a comparative assessment with the available alternatives. For each glyphosate-based product, all uses for which there is an alternative that meets the substitution criteria will therefore be prohibited.

France - Agence Nationale du Médicament Vétérinaire

29-11-2018

ANSES and CEA join forces to strengthen technological innovation in order to safeguard health

ANSES and CEA join forces to strengthen technological innovation in order to safeguard health

During the symposium organised to mark the sixtieth anniversary of the creation of the ANSES Laboratory in Ploufragan (Côtes d'Armor), on Thursday 29 November 2018, Roger Genet, Director General of ANSES, and Stéphane Siebert, Director of Technological Research at the CEA, signed a framework partnership agreement aimed at strengthening their cooperation to develop innovative technological tools in order to improve responsiveness in the fields of animal and plant health and food safety.

France - Agence Nationale du Médicament Vétérinaire

29-11-2018

MPS Canada Corporation recalls various Consumer chemical products in pressurized containers

MPS Canada Corporation recalls various Consumer chemical products in pressurized containers

The recalled products were not destined for the Canadian marketplace and do not have mandatory hazard labelling as required by the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. Improper labelling could result in unintentional exposure to these products and lead to serious illness, injury or death.

Health Canada

20-12-2018

.@US_FDA provides an update on new steps to revise #Essure's post-market study to collect long-term safety information following discontinuation of its U.S. sales. Read FDA Commissioner @SGottliebFDA's statement on the new steps here:  https://go.usa.gov/

.@US_FDA provides an update on new steps to revise #Essure's post-market study to collect long-term safety information following discontinuation of its U.S. sales. Read FDA Commissioner @SGottliebFDA's statement on the new steps here: https://go.usa.gov/

. @US_FDA provides an update on new steps to revise #Essure's post-market study to collect long-term safety information following discontinuation of its U.S. sales. Read FDA Commissioner @SGottliebFDA's statement on the new steps here: https://go.usa.gov/xEaNB  #MedicalDevice

FDA - U.S. Food and Drug Administration

20-12-2018

Following Essure’s removal from the market, the FDA will continue to monitor women with device; we’re working to implement surveillance system and registries to answer crucial questions on devices for women’s health.  https://go.usa.gov/xEa9p 

Following Essure’s removal from the market, the FDA will continue to monitor women with device; we’re working to implement surveillance system and registries to answer crucial questions on devices for women’s health. https://go.usa.gov/xEa9p 

Following Essure’s removal from the market, the FDA will continue to monitor women with device; we’re working to implement surveillance system and registries to answer crucial questions on devices for women’s health. https://go.usa.gov/xEa9p 

FDA - U.S. Food and Drug Administration

20-12-2018

The use of necklaces, bracelets,& other jewelry marketed for relieving teething pain can lead to serious injuries or death & should not be used to reduce teething pain in infants or to provide sensory  stimulation to persons with special needs. Learn more

The use of necklaces, bracelets,& other jewelry marketed for relieving teething pain can lead to serious injuries or death & should not be used to reduce teething pain in infants or to provide sensory stimulation to persons with special needs. Learn more

The use of necklaces, bracelets,& other jewelry marketed for relieving teething pain can lead to serious injuries or death & should not be used to reduce teething pain in infants or to provide sensory stimulation to persons with special needs. Learn more: https://go.usa.gov/xEaWn  pic.twitter.com/RScrgBUSYj

FDA - U.S. Food and Drug Administration

14-12-2018


Guidance on the classification of veterinary medicinal products indicated for minor use minor species (MUMS) / limited market - Revsion 2

Guidance on the classification of veterinary medicinal products indicated for minor use minor species (MUMS) / limited market - Revsion 2

Guidance on the classification of veterinary medicinal products indicated for minor use minor species (MUMS) / limited market - Revsion 2

Europe - EMA - European Medicines Agency

14-12-2018

Revinty Ellipta (GlaxoSmithKline (Ireland) Limited)

Revinty Ellipta (GlaxoSmithKline (Ireland) Limited)

Revinty Ellipta (Active substance: fluticasone furoate / vilanterol) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8927 of Fri, 14 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2745/T/38

Europe -DG Health and Food Safety

14-12-2018

Relvar Ellipta (GlaxoSmithKline (Ireland) Limited)

Relvar Ellipta (GlaxoSmithKline (Ireland) Limited)

Relvar Ellipta (Active substance: fluticasone furoate/vilanterol) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8928 of Fri, 14 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2673/T/40

Europe -DG Health and Food Safety

12-12-2018

Oncaspar (Les Laboratoires Servier)

Oncaspar (Les Laboratoires Servier)

Oncaspar (Active substance: pegaspargase) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8757 of Wed, 12 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3789/T/21

Europe -DG Health and Food Safety

11-12-2018

Ziagen (ViiV Healthcare BV)

Ziagen (ViiV Healthcare BV)

Ziagen (Active substance: abacavir sulfate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8685 of Tue, 11 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/252/T/104

Europe -DG Health and Food Safety

11-12-2018

Rubraca (Clovis Oncology Ireland Limited)

Rubraca (Clovis Oncology Ireland Limited)

Rubraca (Active substance: rucaparib) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8686 of Tue, 11 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4272/T/5

Europe -DG Health and Food Safety

10-12-2018

Exondys (AVI BioPharma International Ltd)

Exondys (AVI BioPharma International Ltd)

Exondys (Active substance: eteplirsen) - Centralised - Refusal of marketing authorisation - Commission Decision (2018)8620 of Mon, 10 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4355

Europe -DG Health and Food Safety

7-12-2018

Olanzapine Mylan (Mylan S.A.S.)

Olanzapine Mylan (Mylan S.A.S.)

Olanzapine Mylan (Active substance: Olanzapine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7622 of Fri, 07 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/961/T/45

Europe -DG Health and Food Safety

30-11-2018

Selected participants will work directly with the FDA to accelerate the development of and eventual review of marketing applications for these innovative products. Read more:  https://go.usa.gov/xPMPk pic.twitter.com/6rRnfSyLy4

Selected participants will work directly with the FDA to accelerate the development of and eventual review of marketing applications for these innovative products. Read more: https://go.usa.gov/xPMPk pic.twitter.com/6rRnfSyLy4

Selected participants will work directly with the FDA to accelerate the development of and eventual review of marketing applications for these innovative products. Read more: https://go.usa.gov/xPMPk  pic.twitter.com/6rRnfSyLy4

FDA - U.S. Food and Drug Administration

29-11-2018

alli (GlaxoSmithKline Dungarvan Limited)

alli (GlaxoSmithKline Dungarvan Limited)

alli (Active substance: Orlistat) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8041 of Thu, 29 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/854/T/59

Europe -DG Health and Food Safety

28-11-2018

Docetaxel Zentiva (Zentiva k.s.)

Docetaxel Zentiva (Zentiva k.s.)

Docetaxel Zentiva (Active substance: Docetaxel) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8039 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/808/T/56

Europe -DG Health and Food Safety

28-11-2018

Econor (Elanco GmbH)

Econor (Elanco GmbH)

Econor (Active substance: Valnemulin hydrochloride) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8038 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/42/T/54

Europe -DG Health and Food Safety

28-11-2018

Zeffix (GlaxoSmithKline (Ireland) Limited)

Zeffix (GlaxoSmithKline (Ireland) Limited)

Zeffix (Active substance: Lamivudine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8044 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/242/T/73

Europe -DG Health and Food Safety

28-11-2018

Orkambi (Vertex Pharmaceuticals (Ireland) Limited)

Orkambi (Vertex Pharmaceuticals (Ireland) Limited)

Orkambi (Active substance: Lumacaftor/Ivacaftor) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8042 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3954/T/39

Europe -DG Health and Food Safety

28-11-2018

PHEBURANE (Eurocept International BV)

PHEBURANE (Eurocept International BV)

PHEBURANE (Active substance: Sodium Phenylbutyrate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8043 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2500/T/20

Europe -DG Health and Food Safety

28-11-2018

Kalydeco (Vertex Pharmaceuticals (Ireland) Limited)

Kalydeco (Vertex Pharmaceuticals (Ireland) Limited)

Kalydeco (Active substance: ivacaftor) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8047 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2494/T/71

Europe -DG Health and Food Safety

28-11-2018

Use of market authorisation evidence from comparable overseas regulators / assessment bodies for medical devices (including IVDs)

Use of market authorisation evidence from comparable overseas regulators / assessment bodies for medical devices (including IVDs)

Clarification of ISO 13485 certificates for IVD medical devices

Therapeutic Goods Administration - Australia

28-11-2018

Listed medicine compliance rating scheme

Listed medicine compliance rating scheme

We have implemented a Compliance Rating Scheme for listed medicines as part of ongoing enhancements to our post-market compliance monitoring program

Therapeutic Goods Administration - Australia

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

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

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

Europe - EMA - European Medicines Agency