Nu-Lax

Main information

  • Trade name:
  • Nu-Lax Natural Laxative Tablets with Prebiotic
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • Nu-Lax Natural Laxative Tablets with Prebiotic
    Australia
  • Language:
  • English

Other information

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 220218
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:

220218

Nu-Lax Natural Laxative Tablets with Prebiotic

ARTG entry for

Medicine Listed

Sponsor

Orchard Manufacturing Co Pty Ltd

Postal Address

Unit 1/97-101 Bayfield Road East,Bayswater, VIC, 3153

Australia

ARTG Start Date

17/02/2014

Product category

Medicine

Status

Active

Approval area

Listed Medicines

Conditions

Colouring agents used in listed medicine for ingestion, other than those listed for export only under section 25 of the Act, shall be only those included in

the list of 'Colourings permitted in medicines for oral use'.

The sponsor shall keep records relating to this listed medicine as are necessary to: (a) Expedite recall if necessary of any batch of the listed medicine,

(b) Identify the manufacturer(s) of each batch of the listed medicine. Where any part of or step in manufacture in Australia of the listed medicine is

sub-contracted to a third party who is not the sponsor, copies of relevant Good Manufacturing Practice agreements relation to such manufacture shall be

kept.

The sponsor shall retain records of the distribution of the listed medicine for a period of five years and shall provide the records or copies of the records

to the Complementary Medicines Branch, Therapeutic Goods Administration, upon request.

The sponsor of the listed medicine must not, by any means, intentionally or recklessly advertise the medicine for an indication other than those accepted

in relation to the inclusion of the medicine in the Register.

All reports of adverse reactions or similar experiences associated with the use or administration of the listed medicine shall be notified to the Head, Office

of Product Review, Therapeutic Goods Administration, as soon as practicable after the sponsor of the goods becomes aware of those reports. Sponsors

of listed medicines must retain records of such reports for a period of not less than 18 months from the day the Head, Office of Product Review is notified

of the report or reports.

The sponsor shall not supply the listed medicine after the expiry date of the goods.

Where a listed medicine is distributed overseas as well as in Australia, product recall or any other regulatory action taken in relation to the medicine

outside Australia which has or may have relevance to the quality, safety or efficacy of the goods distributed in Australia, must be notified to the National

Manager Therapeutic Goods Administration, immediately the action or information is known to the sponsor.

Products

1. Nu-Lax Natural Laxative Tablets with Prebiotic

Product Type

Single Medicine Product

Effective date

3/10/2016

Warnings

If symptoms persist consult your healthcare practitioner (or words to that effect).

Use in children under 12 years is not recommended.

Do not use when abdominal pain, nausea or vomiting are present, or if you develop diarrhoea. If you are pregnant or breast feeding, seek the advice of a

healthcare professional before taking this product (or words to that effect).

Prolonged use may cause serious bowel problems.

Drink plenty of water (or words to that effect).

Standard Indications

Aids or assists in the relief of constipation. [Warnings S and LAX1 required / LAX2 required in certain circumstances]

Laxative. Aids or assists in the prevention of constipation. [Warnings S and LAX1 required / LAX2 required in certain circumstances]

May assist in the management of constipation. [Warnings S and LAX1 required / LAX2 required in certain circumstances]

For the symptomatic relief of constipation. [Warnings S and LAX1 required / LAX2 required in certain circumstances]

Aids or assists in the treatment of constipation. [Warnings S and LAX1 required / LAX2 required in certain circumstances]

Specific Indications

Aloe barbadensis may help to maintain healthy digestive function and relieve gastrointestinal inflammation. Aloe barbadensis may reduce inflammation in

the gastrointestinal tract. Aloe barbadensis is a prebiotic. Prebiotics improve the survival and implantation of live probiotics for the benefit of the host

health and wellbeing. Aloe barbadensis promotes the growth of "good" bacteria and soothes the irritated lining of the digestive system. Brings overnight

relief, assists regularity and supports normal bowel function. Maintains a healthy digestive function. Relieves constipation and soothes the digestive

system.

Additional Product information

Pack Size/Poison information

Pack Size

Poison Schedule

Components

Public Summary

Page 1 of

Produced at 26.11.2017 at 02:43:23 AEDT

This is not an ARTG Certificate document.

The onus is on the reader to verify the current accuracy of the information on the document subsequent to the date shown.

Visit www.tga.gov.au for contact information

1. Formulation 1

Dosage Form

Tablet, film coated

Route of Administration

Oral

Visual Identification

Active Ingredients

Aloe vera

5 mg

Equivalent: Aloe vera (Juice fresh)

Senna alexandrina

180 mg

Equivalent: Senna alexandrina (Dry)

540 mg

© Commonwealth of Australia.This work is copyright.You are not permitted to re-transmit, distribute or commercialise the material without obtaining prior

written approval from the Commonwealth.Further details can be found at http://www.tga.gov.au/about/website-copyright.htm.

Public Summary

Page 2 of

Produced at 26.11.2017 at 02:43:23 AEDT

This is not an ARTG Certificate document.

The onus is on the reader to verify the current accuracy of the information on the document subsequent to the date shown.

Visit www.tga.gov.au for contact information

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Veraflox (Bayer Animal Health GmbH)

Veraflox (Bayer Animal Health GmbH)

Veraflox (Active substance: Pradofloxacin) - Centralised - Yearly update - Commission Decision (2018)3834 of Wed, 13 Jun 2018

Europe -DG Health and Food Safety

11-6-2018

Bexsero (GlaxoSmithKline Vaccines S.r.l.)

Bexsero (GlaxoSmithKline Vaccines S.r.l.)

Bexsero (Active substance: Meningococcal group B Vaccine (rDNA, component, adsorbed)) - Centralised - 2-Monthly update - Commission Decision (2018)3769 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2333/II/59

Europe -DG Health and Food Safety

4-6-2018

Venclyxto (AbbVie Deutschland GmbH and Co. KG)

Venclyxto (AbbVie Deutschland GmbH and Co. KG)

Venclyxto (Active substance: venetoclax) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3633 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4106/T/12

Europe -DG Health and Food Safety

16-5-2018

EU/3/13/1116 (GlaxoSmithKline Trading Services Limited)

EU/3/13/1116 (GlaxoSmithKline Trading Services Limited)

EU/3/13/1116 (Active substance: Mepolizumab) - Transfer of orphan designation - Commission Decision (2018)3046 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/174/12/T/01

Europe -DG Health and Food Safety

16-5-2018

EU/3/04/213 (GlaxoSmithKline Trading Services Limited)

EU/3/04/213 (GlaxoSmithKline Trading Services Limited)

EU/3/04/213 (Active substance: Mepolizumab) - Transfer of orphan designation - Commission Decision (2018)3045 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/027/04/T/02

Europe -DG Health and Food Safety

16-5-2018

EU/3/17/1954 (AbbVie Deutschland GmbH and Co. KG)

EU/3/17/1954 (AbbVie Deutschland GmbH and Co. KG)

EU/3/17/1954 (Active substance: Venetoclax) - Transfer of orphan designation - Commission Decision (2018)3028 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/131/17/T/01

Europe -DG Health and Food Safety

16-5-2018

EU/3/16/1767 (AbbVie Deutschland GmbH and Co. KG)

EU/3/16/1767 (AbbVie Deutschland GmbH and Co. KG)

EU/3/16/1767 (Active substance: Venetoclax) - Transfer of orphan designation - Commission Decision (2018)3027 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/121/16/T01

Europe -DG Health and Food Safety

16-5-2018

EU/3/16/1766 (AbbVie Deutschland GmbH and Co. KG)

EU/3/16/1766 (AbbVie Deutschland GmbH and Co. KG)

EU/3/16/1766 (Active substance: Venetoclax) - Transfer of orphan designation - Commission Decision (2018)3026 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/122/16/T/01

Europe -DG Health and Food Safety

16-5-2018

EU/3/16/1617 (AbbVie Deutschland GmbH and Co. KG)

EU/3/16/1617 (AbbVie Deutschland GmbH and Co. KG)

EU/3/16/1617 (Active substance: Venetoclax) - Transfer of orphan designation - Commission Decision (2018)3023 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/205/15/T/01

Europe -DG Health and Food Safety

3-5-2018

Avamys (Glaxo Group Ltd)

Avamys (Glaxo Group Ltd)

Avamys (Active substance: Fluticasone furoate) - Centralised - Yearly update - Commission Decision (2018)2773 of Thu, 03 May 2018

Europe -DG Health and Food Safety