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Several species skin care products Used to treat acne are withdrawn due to the risk of cancer.
Products containing benzoil peroxide, usual acne treatment, have been tested to elevated Benzen levels, according to the reports of the America Food and Medication Directorate (FDA).
AND recalled products Include:
- La Roche -Posay Effaclar Duo Dual Action Treatment Against Akni – Lot Myx46w
- Walgreens Akni Control Inspection – Lot Number 23 09328
- Proactiv Emergency Cream Benzoil Peroxide 5% – Lota V3305A number; V3304A
- Proactiv Exofoving Exofoving – Lota V4204A number
- SLMD BENZOIL PEROXID ASCIENCE AGNIA – LOT number 2430600
- Walgreens Darkened Acne Cream – Lot Number 4970743
Several types of skin care products used to treat acne are withdrawn due to the risk of cancer. (East)
Acnni Zapzyt gel manufacturer also agreed that he would voluntarily recall the product due to the elevated Benzen level found in his own testing, the FDA said.
The FDA explained that 90% of 95 products with benzoil peroxide that tested had “undiscovered or extremely low benzene levels”.
Benzen is “a chemical used in the production of a wide range of industrial products, including chemicals, colors, detergents and some plastic,” the Agency states.
It is released into the air through “Cigarette smoke, car emissions and burning coal and oil”.
La Roche-Posay Effaclar Duo Dual Action Treatment Against AKNI with Lot Myx46W number was one of the recalled products. (La Roche-Posay)
Although it is safe to use benzoil peroxide in acne products, benzene contamination in small quantities over a long period of time “can reduce blood cell formation. Long -term exposure to benzene by inhalation, oral intake and absorption of skin can result in cancer such as leukemia and other blood disorders.”
The FDA announced that the independent testing of Benzoil Peroxide products began after the result of third -party tests “caused concern for elevated benzen levels in certain acne products.”
“The results of the FDA test show less products with the contamination of benzen from the findings of third parties,” the agency added.
The FDA announced that the companies voluntarily recalled the products, noting that it was in retail and not at the consumer level. (AP Photo/Andrew Hardik, file)
FDA He said the companies voluntarily recalled the products, noting that it was in retail and not at the consumer level.
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“This means that traders are instructed to remove products from the shelves of stores and online markets, but they do not specifically do not indicate consumers to perform actions regarding the products currently in their possession,” FDA said. “Even with the daily use of these products for decades, the risk of a person developing cancer due to the exposure to the benzen found in these products is very low.”
