BORACOL

Main information

  • Trade name:
  • BORACOL 100RH FUNGICIDE
  • Pharmaceutical form:
  • LIQUID
  • Units in package:
  • 1L,3L,5L,10L,20L,25L,50L,200L,250L,1000L
  • Class:
  • AgChem
  • Medicine domain:
  • Equipment
  • Medicine type:
  • Agrochemical
  • Manufactured by:
  • OSMOSE AUSTRALIA

Documents

Localization

  • Available in:
  • BORACOL 100RH FUNGICIDE
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • CONCRETE | TIMBER | PAINTED CONCRETE | UNPAINTED CONCRETE | WOOD
  • Therapeutic area:
  • Fungicide
  • Therapeutic indications:
  • ALGAE | DECAY PREVENTION OR PRESERVATION | FUNGUS | LICHEN | MOSS | FUNGAL LEAF SPOTS | FUNGI | FUNGUS DISEASES | GIVES LONGER LIFE | LEAF SPOT DISEASES | LEAF SPOTS
  • Product summary:
  • For the treatment of surfaces attacked or susceptible to mould, algae, fungus, lichen and moss etc. Suitable for timber, brickwork, concrete etc. or other surfaces where eradication and/or residual action is required.NOT TO BE USED on surfaces which come into direct contact with the ground.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 30710/0799
  • Authorization date:
  • 28-07-1999
  • Last update:
  • 15-06-2017

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

CAUTION

KEEP OUT OF REACH OF CHILDREN

READ SAFETY DIRECTIONS BEFORE OPENING OR USING

BORACOL 100RH FUNGICIDE

ACTIVE CONSTITUENTS:

23 g/L BORON (B) present as DISODIUM

OCTABORATE TETRAHYDRATE

22 g/L BENZALKONIUM CHLORIDE

SOLVENT:

109 g/L MONOETHYLENE GLYCOL

FOR THE TREATMENT OF SURFACES ATTACKED OR SUSCEPTIBLE TO

MOULD, ALGAE, FUNGUS, LICHEN AND MOSS ETC. SUITABLE FOR

TIMBER, BRICKWORK, CONCRETE ETC. OR OTHER SURFACES WHERE

ERADICATION AND/OR RESIDUAL ACTION IS REQUIRED.

CONTENTS:

1L / 3L / 5L / 10L / 20L / 25L / 50L / 200L / 250L / 1000L

FERNZ TIMBER PROTECTION

Cafpirco Road

(A Division of Fernz Australia Ltd)

Compton via Mount Gambier

ACN 008 433 010

SA 5290

Tel:

(08) 8723 1399

Fax:

(08) 8723 0010

DIRECTIONS FOR USE

RESTRAINTS

NOT TO BE USED on surfaces which come into direct contact with foodstuffs.

NOT TO BE USED on roofs for collection of potable water.

NOT TO BE USED on surfaces which come into direct contact with the ground.

GENERAL INSTRUCTIONS

BORACOL 100RH is effective in controlling surface mould, algae, fungi, lichen and

moss. Applications include marinas, decking, pool surrounds, roofs, fences, walls or

any other surfaces where damp conditions favour growth of attacking organisms.

BORACOL 100RH used at the recommended rate will give a residual effect which

will help prevent re-infestation. The residual effect of BORACOL 100RH will be

enhanced if the applied surface is sealed with a sealer such as a water

repellent/paint/varnish etc.

BORACOL 100RH is supplied ready for use. Surfaces with excessively heavy

infestation should be given a preliminary clean-down using a high pressure water

spray or a stiff brush.

BORACOL 100RH, after correct application, may require up to 48 hours to destroy

the attacking organisms. It is then recommended that the surface is brushed to remove

dead material prior to sealing. BORACOL 100RH can be applied to either dry or

damp surfaces.

APPLICATION TABLE

BORACOL 100RH can be applied by brush, roller, dipping or spraying.

SITUATION

STATES

RECOMMENDATION

Timber, concrete,

brickwork, masonry,

asbestos, cement render,

roofs

ALL STATES

Dependent on surface porosity

160-500mL per square metre (2-

6 square metres per litre).

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

Do not contaminate streams, rivers or waterways with the chemical or used

containers.

STORAGE AND DISPOSAL

Store in original closed container in a dry, cool, well ventilated area. Do not store for

long periods in direct sunlight. DO NOT use the container for any other purpose.

Triple or preferably pressure rinse containers before disposal. Dispose of rinsings in a

disposal pit specifically marked and set up for this purpose, clear of waterways,

desirable vegetation and tree roots.

(For All Pack Sizes except 1000L)

Break, crush or puncture and bury containers in a local authority landfill.

If no landfill is available, bury the containers below 500mm in a disposal pit. Empty

containers and product should not be burnt.

(For 1000L Packsize)

Empty contents fully into application equipment. Close all valves and return to point

of supply for refill or storage.

SAFETY DIRECTIONS

Will irritate the eyes, nose and throat and skin. Avoid contact with eyes and skin. Do

not inhale spray mist. After use and before eating, drinking or smoking, wash hands,

arms and face thoroughly with soap and water.

FIRST AID

If poisoning occurs, contact a doctor or Poisons Information Centre. Phone Australia

131126.

If swallowed, and if more than 15 minutes from a hospital, induce vomiting preferably

using Ipecac Syrup APF.

Additional information is listed in the Material Safety Data Sheet

CONDITIONS OF SALE

Fernz Corporation Ltd. (“Fernz”) shall not be liable for any loss, injury, damage or

death whether consequential or otherwise whatsoever or howsoever arising whether

through negligence or otherwise in connection with the sale, supply, use or

application of this product. The supply of this product is on the express condition that

the purchaser does not rely on Fernz skill or judgment in purchasing or using the same

and every person dealing with this product does so at their own risk absolutely. No

representative of Fernz has any authority to add or alter these conditions.

Batch No.:

Date of Manufacture:

NRA Approval No.: 30710/0799

IN CASE OF EMERGENCY PHONE 1800 088 809

17-1-2019

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The Danish Medicines Agency will be closed between Christmas and New Year from 22 December 2018 to 1 January 2019, both days inclusive. This means that enquiries made to the Danish Medicines Agency, with a few exceptions, will not be read and replied during this period. On this page, you can find the deadlines that apply to applications in the Danish Medicines Agency's area in 2018.

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NEXGARD SPECTRA (Merial)

NEXGARD SPECTRA (Merial)

NEXGARD SPECTRA (Active substance: Afoxolaner / milbemycin oxime) - Centralised - 2-Monthly update - Commission Decision (2018)6977 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/003842/WS1338/0015/G

Europe -DG Health and Food Safety

22-10-2018

EU/3/16/1640 (Celgene Europe B.V.)

EU/3/16/1640 (Celgene Europe B.V.)

EU/3/16/1640 (Active substance: 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl]amino}-1,3,5-triazin-2-yl)amino]propan-2-ol methanesulfonate) - Transfer of orphan designation - Commission Decision (2018)6989 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/253/15/T/01

Europe -DG Health and Food Safety

22-10-2018

EU/3/16/1689 (Alan Boyd Consultants Ltd)

EU/3/16/1689 (Alan Boyd Consultants Ltd)

EU/3/16/1689 (Active substance: Teriparatide) - Transfer of orphan designation - Commission Decision (2018)6987 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/031/16/T/01

Europe -DG Health and Food Safety

22-10-2018

EU/3/01/075 (Eisai GmbH)

EU/3/01/075 (Eisai GmbH)

EU/3/01/075 (Active substance: Denileukin diftitox) - Transfer of orphan designation - Commission Decision (2018)6991 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/038/01/T/02

Europe -DG Health and Food Safety

22-10-2018

Pemetrexed Hospira (Pfizer Europe MA EEIG)

Pemetrexed Hospira (Pfizer Europe MA EEIG)

Pemetrexed Hospira (Active substance: pemetrexed) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6971 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3970/T/14

Europe -DG Health and Food Safety

22-10-2018

Velphoro (Vifor Fresenius Medical Care Renal Pharma France)

Velphoro (Vifor Fresenius Medical Care Renal Pharma France)

Velphoro (Active substance: mixture of polynuclear iron(iii)-oxyhydroxide, sucrose and starches) - Centralised - Yearly update - Commission Decision (2018)6972 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

EU/3/05/264 (Roche Registration GmbH)

EU/3/05/264 (Roche Registration GmbH)

EU/3/05/264 (Active substance: Cholest-4-en-3-one, oxime) - Transfer of orphan designation - Commission Decision (2018)6995 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/OD/081/04/T/02

Europe -DG Health and Food Safety

22-10-2018

EU/3/11/901 (Merck Sharp and Dohme B.V.)

EU/3/11/901 (Merck Sharp and Dohme B.V.)

EU/3/11/901 (Active substance: Dinaciclib) - Transfer of orphan designation - Commission Decision (2018)6990 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/052/11/T/01

Europe -DG Health and Food Safety

22-10-2018

EU/3/15/1495 (Ultragenyx Netherlands B.V.)

EU/3/15/1495 (Ultragenyx Netherlands B.V.)

EU/3/15/1495 (Active substance: Triheptanoin) - Transfer of orphan designation - Commission Decision (2018)6992 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/007/15/T/02

Europe -DG Health and Food Safety

22-10-2018

Evoltra (Genzyme Europe B.V.)

Evoltra (Genzyme Europe B.V.)

Evoltra (Active substance: clofarabine) - Centralised - Yearly update - Commission Decision (2018)6973 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

Irbesartan / Hydrochlorothiazide Teva (Teva B.V.)

Irbesartan / Hydrochlorothiazide Teva (Teva B.V.)

Irbesartan / Hydrochlorothiazide Teva (Active substance: irbesartan / hydrochlorothiazide) - Centralised - Yearly update - Commission Decision (2018) 6974 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

Forsteo (Eli Lilly Nederland B.V.)

Forsteo (Eli Lilly Nederland B.V.)

Forsteo (Active substance: Teriparatide) - Centralised - Yearly update - Commission Decision (2018) 6975 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

EU/3/17/1966 (Sirius Regulatory Consulting EU Limited)

EU/3/17/1966 (Sirius Regulatory Consulting EU Limited)

EU/3/17/1966 (Active substance: N-(bromoacetyl)-3,3-dinitroazetidine) - Transfer of orphan designation - Commission Decision (2018)6986 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

EU/3/15/1532 (Sirius Regulatory Consulting EU Limited)

EU/3/15/1532 (Sirius Regulatory Consulting EU Limited)

EU/3/15/1532 (Active substance: Insulin human) - Transfer of orphan designation - Commission Decision (2018)6985 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

EU/3/16/1704 (Drug Development and Regulation S.L.)

EU/3/16/1704 (Drug Development and Regulation S.L.)

EU/3/16/1704 (Active substance: Sirolimus) - Transfer of orphan designation - Commission Decision (2018)6988 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/045/16/T/01

Europe -DG Health and Food Safety

22-10-2018

EU/3/10/815 (Pfizer Europe MA EEIG)

EU/3/10/815 (Pfizer Europe MA EEIG)

EU/3/10/815 (Active substance: Sildenafil citrate) - Transfer of orphan designation - Commission Decision (2018)6993 of Mon, 22 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/068/10/T/01

Europe -DG Health and Food Safety