Recall children's Lesgo mouthwash water for violating ingredient disclosure

Hà Lê |

The Ministry of Health recalls Lesgo children's mouthwash nationwide due to containing ingredients other than the advertised formula.

The Drug Administration of Vietnam (Ministry of Health) issued a decision to suspend the circulation, recall and destroy nationwide the batch of children's Lesgo Mouth Drink - 150 ml bottle produced by Ellie Joint Stock Company for detecting substances that were not in accordance with the advertised formula.

According to information from the Drug Administration of Vietnam (Ministry of Health), Lesgo Children's Ganetana Products - 150 ml bottle (receiving number of published notes: 2083/22/CBMP -HCM, Lot number: 0426230724, NSX: 23.7.2024, HSD: 23.7.2027) by ELLIE Joint Stock Company, which is responsible for producing and putting on the market. This ingredient is not included in the product formula that has been granted the number of cosmetic releases.

The test sample was taken by the Center for Drug, Cosmetic and Food Testing - Ho Chi Minh City Department of Food Safety at CoopXtra Tan Phong supermarket (SC Vivo City, Ho Chi Minh City). The analysis results showed that the product violated regulations on cosmetic management according to Circular No. 06/2011/TT-BYT of the Ministry of Health.

The Drug Administration of Vietnam requires the Departments of Health of provinces and cities to notify businesses and users to immediately stop the circulation and use of the above product batch; at the same time, recall and destroy all violating goods and strictly handle non-compliant units.

Ellie Joint Stock Company must notify all distributors and users of the product of the recall; receive the returned goods; organize the destruction and report the results to the Drug Administration before September 20, 2025.

The Ho Chi Minh City Department of Health closely monitors the recovery and destruction of enterprises; at the same time, revokes the receipt number of the cosmetic product declaration form 2083/22/CBMP-HCM and conducts inspections and handling violations according to regulations. Report the results to the Department of Drug Administration before October 5, 2025.

Hà Lê
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