CODRAL COLD & FLU oral powder sachet

Main information

  • Trade name:
  • CODRAL COLD & FLU oral powder sachet
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • CODRAL COLD & FLU oral powder sachet
    Australia
  • Language:
  • English

Status

  • Source:
  • Dept. of Health,Therapeutic Goods Administration - Australia
  • Authorization status:
  • Registered
  • Authorization number:
  • 181442
  • Last update:
  • 22-05-2019

Public Assessment Report

Public Summary

Summary for ARTG Entry:

181442

CODRAL RELIEF MAX COLD & FLU + DECONGESTANT Hot Drink oral powder sachet

ARTG entry for

Medicine Registered

Sponsor

Johnson & Johnson Pacific Pty Ltd

Postal Address

Locked Bag 5,

BROADWAY, NSW, 2007

Australia

ARTG Start Date

25/03/2011

Product category

Medicine

Status

Active

Approval area

Non-Prescription Medicines

Conditions

Conditions applicable to all therapeutic goods as specified in the document "Standard Conditions Applying to Registered or Listed Therapeutic Goods

Under Section 28 of the Therapeutic Goods Act 1989" effective 1 July 1995.

Conditions applicable to the relevant category and class of therapeutic goods as specified in the document "Standard Conditions Applying to Registered

or Listed Therapeutic Goods Under Section 28 of the Therapeutic Goods Act 1989" effective 1 July 1995.

Products

1. CODRAL RELIEF MAX COLD & FLU + DECONGESTANT Hot Drink oral powder sachet

Product Type

Single Medicine Product

Effective date

2/03/2016

Warnings

No Warnings included on Record

Standard Indications

Specific Indications

For relief of blocked or runny noses, sore throat, headache and body aches and pains associated with cold and flu. Reduces fever.

Additional Product information

Container information

Type

Material

Life Time

Temperature

Closure

Conditions

Sachet

Not recorded

3 Years

Store below 25

degrees Celsius

Not recorded

Not recorded

Pack Size/Poison information

Pack Size

Poison Schedule

10 sachets (with backing card)

Not Scheduled after consideration by Committee

10 sachets

Not Scheduled after consideration by Committee

Components

1.

Dosage Form

Powder, oral

Route of Administration

Oral

Visual Identification

Yellow, free flowing powder.

Active Ingredients

Paracetamol

1000 mg

Phenylephrine hydrochloride

12.2 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 1 of

Produced at 29.11.2017 at 07:43:36 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