Product description
Neutrogena Ultra Sheer Sunscreen Spray SPF 50+ with Helioplex 140g
SAP Code: 28422031
TUN: 19300607560821
IUN: 29300607560828
AUST L 202301
All batches with an expiry date of 30-Aug-2023 or earlier.
ARTG 202301
(Neutrogena Ultra Sheer Sunscreen Spray SPF 50+ with Helioplex)
Only the aerosol spray product is affected. This recall does not affect any other Ultra Sheer or Neutrogena sun care products.
SAP Code: 28422031
TUN: 19300607560821
IUN: 29300607560828
AUST L 202301
All batches with an expiry date of 30-Aug-2023 or earlier.
ARTG 202301
(Neutrogena Ultra Sheer Sunscreen Spray SPF 50+ with Helioplex)
Only the aerosol spray product is affected. This recall does not affect any other Ultra Sheer or Neutrogena sun care products.
See a list of details to help identify the product
Reason the product is recalled
The chemical benzene has been identified in batches of the product. Benzene is not an ingredient listed for inclusion within the product.
The hazards to consumers
Exposure to benzene can be linked to adverse health effects. Benzene is a recognised carcinogen (substance that could potentially cause cancer).
What consumers should do
Consumers should stop using the product and dispose of it. Consumers should visit the website www.neutrogena.com.au to request a refund.
Consumers concerned about their health after using this product, should seek medical advice.
For more information, consumers can contact the Johnson & Johnson Consumer Care Centre
on 1800 789 348.
Consumers concerned about their health after using this product, should seek medical advice.
For more information, consumers can contact the Johnson & Johnson Consumer Care Centre
on 1800 789 348.
Details to help identify the product
Supplier running the recall
Who sold the product
Retail stores and pharmacies nationally
Identifying numbers
Barcode number
9300607560824
Where the product was sold
Nationally
Online
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2021/19147 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.