Product description
Batch Number 11256, Expiry Date: February, 2003. Aust R 50239. The batch number is located on the tuck-in flap on the bottom of the box and on the blister pack.
See a list of details to help identify the product
Reason the product is recalled
One or more Nightime tablets may have been incorrectly positioned in the Daytime section of the blister pack. Nightime caplets should be taken at bed time as they may cause drowsiness.
What consumers should do
If you have a packet of Orthoxicol Day and Night 24 Cold and Flu Caplets from batch 11256 please call our free call number 1800 789 348 to arrange the return of the affected product for a replacement product OR return to Johnson & Johnson Pacific Pty Ltd.
Details to help identify the product
Supplier running the recall
Johnson & Johnson Pacific Pty Ltd
Where the product was sold
Nationally
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2002/5804 when contacting a regulator about this recall.
Recall and remedy questions
Contact the Therapeutic Goods Administration if you have:
- a question about the remedy being offered to you by the business that is responsible for managing this recall, or
- concerns about the way the business is managing this recall.