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Health Sciences Authority
Product Recalls

皮得康 DERMATITIS CREAM SKIN ITCHING CREAM (EXTERNAL)

Audiences

Healthcare professional

Industry member

Product type

Chinese Proprietary Medicines

Cosmetic products

Health supplements

Traditional medicines

23 July 2025

Consumer-level recall of 皮得康 DERMATITIS CREAM SKIN ITCHING CREAM (EXTERNAL) due to Clobetasol propionate and Miconazole detected.

This article has been migrated from an earlier version of the site and may display formatting inconsistencies.

Recall details

Date of Recall:

23 July 2025

Product:

皮得康 DERMATITIS CREAM SKIN ITCHING CREAM (EXTERNAL)

Product Category:

Medicated Balm

Batch No.:

All Batches

Class of Recall:

1

Level of Recall:

Consumer

Local Company:

Da Zhong Tang Pte. Ltd. / Chinese Medical Centre Pte. Ltd.

Description of Issue:

The product was tested under HSA’s product quality surveillance programme and was found to contain Clobetasol propionate and Miconazole.

Recall Instructions:

Consumers:
Consumers are advised to see a doctor as soon as possible if they are using the product. Sudden stopping of the steroid-containing creams without medical supervision may worsen underlying skin conditions or cause topical steroid withdrawal symptoms which present as burning, redness, itching, pain or skin peeling. Return the product to retailer or seller whom they have purchased from.

Retail and wholesale suppliers:
Stop supplying the product and return the remaining stocks to the company.

Pidekang Dermatitis Cream tube showing front label with product name
Pidekang Dermatitis Cream tube showing back label with usage instructions
Open jar of Pidekang Dermatitis Cream showing yellow-green cream contents

Note: 

The Health Sciences Authority (HSA) publishes information regarding recalls of health products supplied in Singapore. These product recalls may be conducted on a company’s own initiative or upon HSA’s request to remove products where there are issues with quality, safety or efficacy. 

When a recall is initiated, it does not necessarily imply that a product is considered unsafe or is inefficacious. A recall can also be initiated to remove products with quality defects that does not impact safety or efficacy from the market so as to ensure that products registered in Singapore continue to meet the stringent regulatory standards stipulated by HSA.

Not all recalls will lead to press releases. However, when a recall involves a product that has been widely distributed or a product that poses a serious health risk, HSA will issue a press release to inform members of public.

Class of recall

A recall is classified as Class 1 or Class 2 depending on the potential hazard of the issue.

  • Class 1: For recalls of products with issues that can potentially cause serious adverse health outcomes or death.

  • Class 2: For recalls of products with issues that would not likely cause serious adverse health outcomes.

Level of recall

The level of product recall will depend on the potential hazard of the affected product, extent of distribution and whether other mitigating measures can be taken to address the issue.

  1. Consumer level: Affected product or batch(es) recalled from patients and consumers as well as wholesale suppliers, retail suppliers, hospitals, clinics and pharmacies.

  2. Retail level: Affected product or batch(es) recalled from retail suppliers, hospitals, clinics and pharmacies as well as wholesale suppliers.

  3. Wholesale level: Affected product or batch(es) recalled from wholesale suppliers.

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