Probiotic

Main information

Documents

Localization

  • Available in:
  • Probiotic Advanced
    Australia
  • Language:
  • English

Other information

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization number:
  • 220114
  • Last update:
  • 08-10-2017

Public Assessment Report

Public Summary

Summary for ARTG Entry:

220114

Probiotic Advanced

ARTG entry for

Medicine Listed

Sponsor

Global Therapeutics Pty Ltd

Postal Address

Commercial 1 57-61 Rothschild Avenue,ROSEBERY, NSW, 2018

Australia

ARTG Start Date

13/02/2014

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. Probiotic Advanced

Product Type

Single Medicine Product

Effective date

12/05/2016

Warnings

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

Adults only. OR Not to be used in children under two years of age without medical advice (or words to that effect).

Standard Indications

Aids or assists in the relief of flatulence. [Warning S required]

May assist in the management of eczema. [Warning S required]

Aids digestion.

Aids, assists or helps in the maintenance or improvement of general well-being.

Helps maintain healthy digestive function.

Specific Indications

Probiotics seem to change how the immune system reacts to invading microorganisms. They may compete with harmful/ bad gut bacteria and promote a

healthy immune system. They may help restore and maintain proper/ healthy bacteria/ microflora balance/ ecology in the intestines, which can be upset

by certain medications, antibiotics and invading microorganisms.

Promotes/supports healthy gastrointestinal/ intestinal microflora/ flora/ ecology/ function

Helps maintain/ restore normal/ healthy/ balanced intestinal/ gut flora

Strong adherence to human intestinal mucosa/ epithelium/ cell lining

Helps maintain/ improve intestinal barrier/ integrity of gut lining

Competes with/ helps inhibit (growth/colonisation of) opportunistic microorganisms/ bad bacteria (in the gut)

Helps reduce abdominal bloating/ gas/ flatulence and discomfort

Improves faecal properties and gut ecology

Promotes gastrointestinal/ intestinal/ colonic health and wellbeing

Supports/maintains normal/ healthy digestive/ gastrointestinal/ bowel function

Benefits immune function to promote gastrointestinal and respiratory health

Public Summary

Page 1 of

Produced at 26.11.2017 at 02:48:57 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

Improves bowel movements.

Supports healthy bowel movements

Promotes normal transit time through the gastrointestinal tract

Resistant to (environmental) factors including stomach acid, bile salts and digestive enzymes incl. pepsin and pancreatin

Assists in the maintenance of normal faecal microbiota from disruption by antibiotics

Helps maintain and more rapidly restore microbiota/ microflora after antibiotic use

Helps restore healthy digestive function after antibiotic use

Supports healthy immune function/ system

Helps maintain a normal/ healthy immune system

Contains clinically researched HOWARU® HN019 and HN001, and FloraFIT® Bl-04 strains

May reduce the risk/incidence of upper respiratory tract infections

Additional Product information

Pack Size/Poison information

Pack Size

Poison Schedule

Components

1. Formulation 1

Dosage Form

Capsule, hard

Route of Administration

Oral

Visual Identification

Active Ingredients

Bifidobacterium animalis ssp lactis

4 billion CFU

Bifidobacterium animalis ssp lactis

3 billion CFU

Lactobacillus acidophilus

12 billion CFU

Lactobacillus plantarum

7 billion CFU

Lactobacillus rhamnosus

2 billion CFU

Lactobacillus rhamnosus

2 billion CFU

© 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 02:48:57 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

31-10-2018

Safety and efficacy of Lactobacillus hilgardii CNCM I‐4785 and Lactobacillus buchneri CNCM I‐4323/NCIMB 40788 as a silage additive for all animal species

Safety and efficacy of Lactobacillus hilgardii CNCM I‐4785 and Lactobacillus buchneri CNCM I‐4323/NCIMB 40788 as a silage additive for all animal species

Published on: Tue, 30 Oct 2018 00:00:00 +0100 Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed was asked to deliver a scientific opinion on the safety and efficacy of a strain of Lactobacillus hilgardii and of Lactobacillus buchneri when used as a technological additive intended to improve ensiling at a proposed application rate of 3.0 x 108 colony forming units (CFU)/kg fresh material. The two bacterial species are considered by EFS...

Europe - EFSA - European Food Safety Authority Publications

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