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Many types of skincare products used to treat acne have been called back due to the risk of cancer.
The US Food and Drug Administration (FDA) said in a notice this week, the products that have a common treatment for acne are benzoyal peroxide, which had a common treatment for acne.
The products called back include:
- La Roshe – Posa Eiffeller duo Dual Action Acne Treatment – A lot of numbers Myx46W
- Walgreens acne control cleanser – a lot of number 23 09328
- Proactiv emergency blemish relight cream benzoyl peroxide 5% – lot number v3305a; V3304a
- Processive skin smoothing exfoliator – lot number v4204a
- Slmd benzoyl peroxide acne lotion – a lot of number 2430600
- Walgreens tinted acne treatment cream – lot number 4970743
The FDA remembers the common Chinese food component after the undeclared sulfate found in the Florida inspection
Many types of skincare products used to treat acne have been called back at the risk of cancer. (Istock)
The FDA stated that the manufacturer of Zapazite Acne Treatment Gel also agreed to voluntarily remember the product due to a high level of benzene found in his own test.
The FDA reported that 95% of 95 products with benzoyal peroxide were tested, “benzene’s” was undesirable or extremely low levels. ,
According to the agency, benzene is a “chemical used in the production of a wide range of industrial products including chemicals, chemicals, chemicals, detergents and some plastic.”
The new report states
It is released in the air through “cigarette smoke, automobile emissions and coal and oil burning”.
La Roche-Posay Effaclar duo dual action acne treatment was one of the products called back with a large number of Myx46W. (La Roshe-Passer)
While it is safe to use benzoyal peroxide in acne products, prolonged amount of benzene contamination “can reduce the formation of blood cells. Long -term contact for benzene can occur for benzene through breathing, oral intake and skin absorption.
The FDA stated that it began an independent test of benzoyal peroxide products following the results of the third party testing, “some acne products increased concerns about the high levels of benzene in some acne products.”
The agency said, “FDA test results indicate less products with benzene contamination compared to third party findings.”
The FDA said that the companies voluntarily recalled the products, given that it was at the retail level and not at the consumer level. (AP Photo/Andrew Harnik, File)
The FDA said that the companies voluntarily recalled the products, given that it was at the retail level and not at the consumer level.
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“This means that retailers are instructed to remove products from store shelves and online marketplaces, but do not instruct consumers to take action about the products in their possession,” the FDA said. “With the daily use of these products for decades, the risk of a person developing cancer is very low due to exposure to the benzene found in these products.”
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