Spray of the athlete's foot recalled on a chemical cancer cancer, the FDA warns
The over -the -counter antifungal treatment is taken from the shelves nationwide due to carcinogen.
Whether you are a passionate trail runner or just spend a lot of time shopping, making sure that your feet are in good shape are essential to spend the day comfortably. Most common problems involve finding the right shoes, get rid of painful , or avoid habits that could cause injuries around the house. But now the US Food & Drug Administration (FDA) warns that a spray on foot has been recalled in stores because it contains a chemical cancer of cancer. Read the rest to see which product is affected and what it could mean for you.
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The FDA announced that an antifungal spray had just been recalled from the market.
On November 24, the FDA published an opinion that Insight Pharmaceuticals had voluntarily recalled two lots of its ting to 2% nitrate nitrate nitrate athlete of antifungal spray powder. The product was distributed to "limited retailers" nationally and sold online in the United States in the United States
The affected elements include the National Drug Code (NDC) 63736-532-05 on the label. The recall affects sprays wrapped in 4.5 ounce spray bottles with the Lot code 0h88645 and the expiration date 07/24, as well as the Lot code 0B88345 and the expiration date 02/24.
The alert specifies that the codes are printed at the bottom of the box. The recall does not affect any other product or lot of the company range.
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Sprays contain high levels of benzene, a chemical cancer cancer.
In his opinion, Insight Pharmaceuticals said that he had initiated the recall after a recent examination carried out by its manufacturer and a third -party laboratory found that the product contained high levels of benzene in affected land.
"Although benzene is not an ingredient in any ting antifungal spray product, the review has shown that unexpected benzene levels came from the propellant that spreads the product out of the box," wrote the company.
Even if it is present in our daily environment from various sources, benzene is a dangerous chemical Classified as a human carcinogen who can cause leukemia, blood cancer of the bone marrow and other blood disorders which "can be fatal", according to the FDA. Exposure can occur orally, topically through the skin and by inhalation.
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Here is what you need to do if you have the sprays recalled at home.
Insight Pharmaceuticals says that there has been no report of "serious undesirable events" linked to the spray on foot recalled so far. He also alerted the sellers and retailers of the problem and asked them to draw the remaining products from the store shelves. AE0FCC31AE342FD3A1346EBB1F342FCB
However, the Company says that all customers who bought the items concerned should stop using them immediately and take a photo of the product's code code. Customers can then send the image to Insight Pharmaceuticals for a full refund.
The company also urges people who believe they have experienced unwanted reactions of product use to immediately contact their health care provider. Anyone with questions or concerns about the spray can also reach the company through the contact details provided on the FDA reminder notice.
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There have been other over -the -counter medicine reminders recently.
Ting antifungal spray is not the only over -the -counter medication (OTC) recalled in recent weeks. At the end of last month, the FDA issued consumers not to buy or continue to use a list of 26 Eye drop products Marketed under CVS health, the leader (Cardinal Health), Rugby (Cardinal Health), Rite Aid, Target Up & Up and Velocity Pharma Brands.
According to an agency survey, the articles manufacturing sites had insanitary conditions . The survey also discovered "the results of positive bacterial tests for the environmental sampling of critical areas for the production of drugs in the installation" for contamination which could cause "ocular infections that could cause partial vision loss or a blindness".
And on November 17, the agency issued an alert that Kinderfarms, LLC had voluntarily recalled two of his pain medication and OTC fever made for children and infants who were sold nationally. In this case, the company said it pulled the products Shelves due to potential "instability" problems with the active ingredient of drugs, acetaminophen, which "may present a health risk".
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