To date, artnaturals has not responded to multiple FDA attempts to discuss the contaminated hand sanitizers, including identification of the manufacturer, possible recalls, and the scope of the contamination. The agency urges consumers not to use this contaminated product and has added artnaturals hand sanitizer products to thelistof hand sanitizers consumers should not use. Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. Sophora Extract Generally, all manufacturers and compounders that produce drugs containing ethanol must conduct the limit test for methanol, using the test method that appears in the USP Alcohol monograph. FDA encourages health ce professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAs MedWatch Adverse Event Reporting program (please provide the agency with as much information as possible to identify the product): [7-2-2020] FDA is warning consumers and health care providers that the agency has seen a sharp increase in hand sanitizer productsthat are labeled to contain ethanol (also known as ethyl alcohol) but that have tested positive for methanol contamination. Transliquid. Last updated on May 17, 2022. Instant action with safe ingredients - no Triclosan, Sulfates, Parabens or Synthetics. 74721-0001-0 Is being recalled by the manufacturer or distributor. Hand Sanitizer Topical Solution, Alcohol Antiseptic 80%, 75293-001-02 Drivergent Hand Sanitizer, 80% Alcohol Antiseptic Topical Hand Rub, Non-Sterile, 1 Quart, 32 FL OZ (0.95 L), Drivergent Hand Sanitizer 70% Alcohol Antiseptic Topical Hand Rub, Non-Sterile Solution, Gel, 8 FL OZ (250 ml), Drivergent Hand Sanitizer, 70% Alcohol Antiseptic Topical Hand Rub, Non-Sterile Solution. Has been tested and is found to have microbial contamination. FDA tested product; contains unacceptable levels of acetaldehyde and acetal;Company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality and the scope of the contamination; FDA recommended the company recall on 1/24/2023. 74721-0002-3 UL did not test, certify, or approve the substance described in this SDS, and CNN . FDA tested product; contains unacceptable levels of acetaldehyde and acetal; company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality, and the scope of the contamination. FDA tested product; contains unacceptable levels of acetaldehyde and acetal; after FDA contacted the firm, firms testing identified benzene in another product. This organic hand sanitizer, which contains 62% alcohol, is formulated with glycerin and dimethicone, which together help hydrate and moisturize the skin, according to EO . Free shipping. 75821-001-03 74530-013-04 Hand sanitizer recall: FDA expands list of 'toxic' sanitizers to avoid over methanol risk by: Alexa Mae Asperin. Hand Sanitizer Sold Nationwide Recalled Due to Health Concerns, FDA Warns 79279-521-04 Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. 74721-0020-0 The agency tweeted on Monday about the two latest recalls. Now, about five dozen different. Do not pour these products down the drain or flush them. PDF Safety Data Sheet - ULINE 80969-010-06 FDA says not to use this hand sanitizer, may contain cancer - KRON4 The FDA's list of dangerous hand sanitizers has now grown to - CNN Consumers who have products on thelist of hand sanitizerswith potential contamination should immediately stop using the product and dispose of it, ideally in ahazardous waste container. Guangdong Theaoson Technology Co. Ltd. (China), Guangdong Theaoson Technology Co., Ltd. Acetal can irritate the upper respiratory tract, eyes, and skin. The agency continues to add certain hand sanitizers to theimport alertto stop these products from legally entering the U.S. market and has issued warning letters to companies that violate federal law. (Mexico), SQ2SKIN Skin Care, Antiseptic Hand Sanitizer Foam (Benzalkonium Chloride 0.13%), 79279-420-01 Grapefruit Extract, 74721-0010-1 Add to cart. 74046-001-10 The testing method (with appropriate validation) can be used for hand sanitizers labeled with either alcohol (ethanol) or isopropyl alcohol (also called isopropanol or 2-propanol) as the active ingredient and can screen for potentially harmful impurities, as listed in FDAs temporary guidances. Durisan tested its hand sanitizer and found microbial contamination including high levels of Burkholderia cepacia complex and Ralstonia pickettii, which can lead to serious infections, including infection of the skin, soft tissues, lungs or bloodstream. The Colorado-based company issued a voluntary recall of 20 lots of Adam's Polishes Hand Sanitizer to the consumer level in "an abundance of caution" after the FDA found one lot had contained. FDA Expands List of Hand Sanitizers That Contain Toxic - Healthline 80969-020-04 74530-012-04 Lukas Flippo, Photo Editor. FDA Adds 4 Brands Of Hand Sanitizer To Growing Recall List 8 Pack 80% Alcohol Naturewell Advanced Liquid Hand Sanitizer Made In USA. It also reported that Target sold Born Basic Anti-Bac Hand Sanitizer, while Walmart sold Scent Theory at stores in 17 states. Contact your local waste management and recycling center for more information on hazardous waste disposal. Is purportedly made at the same facility as products that have been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. FDA Recalls Dozens of Toxic Hand Sanitizers - EcoWatch The agency is aware of adults and children ingesting hand sanitizer products contaminated with methanol that has led to recent adverse events including blindness, hospitalizations and death. Product contains methanol based on information provided by the manufacturer. The product, which contains 70% ethyl alcohol gel, comes in 8-ounce bottles and is intended to be . 79279-620-02 Flavor Vapors, LLC, dba: Mob Liquid Labs GSD Hand Sanitizer And Disinfecting Wipes - FDA Approved GSD All-Purpose Anti-Bacterial Wipes | 80 Wipes per Packet The agency continues to add certain hand sanitizers to import alert to stop these products from legally entering the U.S. market. The company announced the recall on Mar. FDA recommended the company recall on 06/01/2022. Although all persons using these products on their hands are at risk for methanol poisoning, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk. 79279-421-06 Product purported to be made at the same facility that produced an acetaldehyde and acetal contaminated product. Consumers who have been exposed to hand sanitizer containing 1-propanol and are experiencing symptoms should seek immediate care for treatment of toxic effects of 1-propanol poisoning. These 75 Hand Sanitizers Have Been Recalled By The FDA For - Forbes 71120-112-11 FDA updates on hand sanitizers consumers should not use | FDA Sophora Extract Individual Warp Wipes can use anywhere you need to clean hands or there's no water available. List of antiseptic or antibacterial skin cleansers or hand sanitizers meeting Health Canada's requirements for safety, effectiveness and quality, for use against coronavirus (COVID-19). CLARKSBURG, W.Va. (WBOY) A hand sanitizer that was sold over the internet nationwide is being recalled because the company that manufactured it says it may have been contaminated with a toxic chemical. Report any health product adverse events or complaints to Health Canada. Health Canada has suspended the product licence for two of . Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. The Food and Drug Administration has expanded the list of hand sanitizers some sold at Walmart, Costco and other national chains being recalled to at least 75 recently, saying toxic. Health Canada warns about certain hand sanitizers that may pose health Canada's health agency has added three more hand sanitizer products to its growing list of 48 recalled items which began in the spring of 2021. Add to Cart Overview GSD Liquid Hand Sanitizer kills more than 99.99% of the most common germs. The agency urges consumers not to use these subpotent products and has expanded its list to include subpotent hand sanitizers, in addition to hand sanitizers that are or may be contaminated with methanol. Carcinogen found in hand sanitizer distributed by Yale Herbacil Antiseptic Hand Sanitizer 70% Alcohol, FDA tested product; contains methanol; FDA recommended the company recall on 7/24/2020; product voluntarily, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/24/2020; product voluntarily, Soho Fresh Hand Sanitizer Gel Antibacterial, FDA tested product; contains methanol; FDA recommended the company recall on 9/15/2020; added manufacturer to, SOHO Fresh Hand Sanitizer Gel Antibacterial, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 9/15/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; Product voluntarily recalled by, CALA Advanced Hand Sanitizer with Aloe Vera Extract, FDA-tested product; contains benzene; FDA recommended the company recall Lot 2004718 (Expiration 04/2023) on 12/27/2021; FDA expanded recall on 2/25/2022 to include all hand sanitizer drug products manufactured at the facility; added manufacturer to, Earths Amenities Instant Unscented Hand Sanitizer with Aloe Vera Advanced, FDA tested product; contains methanol; product retained at the border; FDA recommended the company recall of all other potential products on the market on 6/29/2020; added manufacturer to, FDA tested product; contains methanol; FDA recommended the company recall of all other potential products on the market on 6/29/2020; added manufacturer to, Vidanos Easy Cleaning Rentals Hand Sanitizer Agavespa Skincare, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall of all other potential products on the market on 6/29/2020; added manufacturer to, DEPQ Internacional S de RL de CV (Mexico), FDA tested product; benzalkonium chloride level was subpotent; FDA has no evidence this product is in the U.S. market; added manufacturer to, dgreen Advanced Hand Sanitizer Antibacterial Gel, Product purported to be made at the same facility that produced subpotent benzalkonium chloride product; FDA has no evidence this product is in the U.S. market; added manufacturer to, FDA tested product; contains methanol; addedmanufacturerto, Product purported to be made at the same facility that produced methanol contaminated product; addedmanufacturerto, Distribuidora Lagunera del Norte SA de CV (Mexico), FDA tested product; ethyl alcohol level was subpotent; FDA has no evidence this product is in the U.S. market; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA has no evidence this product is in the U.S. market; added manufacturer to, Distribuidora Lagunera del Norte SA de CV, FDA tested product; contains methanol; FDA recommended the company recall on 8/21/2020; added manufacturer to, Cleaner by Crystalware Hand Sanitizer Alcohol Gel, FDA tested product; FDA recommended the company recall on 8/21/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 8/21/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; contains methanol; FDA recommended the company recall on 8/21/2020; added manufacturer to, CleanCare NoGerm Advanced Hand Sanitizer 75% Alcohol, FDA tested product; contains methanol; FDA recommended the company recall on 6/17/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall all other products potentially on the market on 6/17/2020; product voluntarily recalled by, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall all other products potentially on the market on 6/17/2020; added manufacturer to, The Good Gel Antibacterial Gel Hand Sanitizer, CleanCare NoGerm Advanced Hand Sanitizer 80% Alcohol, Estrategia Hospitalaria SA de CV (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 8/5/2020; added manufacturer to, Gaza Proveedora de Servicios de Hospedaje y Alimentacion (Mexico), FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 11/20/2020; product voluntarily recalled on 12/1/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 11/20/2020; product voluntarily recalled on 12/1/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 11/20/2020; product voluntarily recalled on 12/8/2020; added manufacturer to, Genesis Partnership Company SA (Guatemala), FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 8/27/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 8/27/2020; added manufacturer to. 1-propanol, not to be confused with 2-propanol/isopropanol/isopropyl alcohol, is not an acceptable ingredient for hand sanitizer products marketed in the United States and can be toxic and life-threatening when ingested. 74530-015-04 There's a nationwide spray hand sanitizer recall on 11 products that were sold at Ulta, TJ Maxx, and Marshalls stores. This comes after a series of recalls related to. Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. Certain hand sanitizers are being recalled because they do not meet Health Canada's requirements. FDA remains vigilant and will continue to take action when quality issues arise with hand sanitizers. 74530-013-05 Hand sanitizer recall: A cancer-causing chemical was found in this The newest recalled hand sanitizers are: Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 01/05/2023, 74046-004-01 75339-751-04 Children are particularly at risk with these products since ingesting only a small amount of hand sanitizer may be lethal in a young child. 74721-0010-6 Health Canada has recalled several hand sanitizers across the country over the last two years over concerns of potential health risks from using the products. Product purported to be made at the same facility that produced product containing acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. The agencys investigation of contaminated hand sanitizers is ongoing. 79279-610-04 74530-012-03 74046-006-10. 80969-020-03 71120-112-05 The temporary guidances have also been updated to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities. Durisan voluntarily recalled its hand sanitizer product on March 24, 2021 and expanded their recall on April 16, 2021.. 74046-001-17 FDA tested product; contains unacceptable levels of acetal; Company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality and the scope of the contamination. Hand Sanitizer Sold Nationwide Recalled Due to Health Concerns, FDA Warns Even though it's long been available to customers, the COVID-19 pandemic certainly changed the rate at which we buy. About this item No animal testing for beauty products 3rd-party certification required for organic claims on body care products Product Description Body Care Product details First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. GSD Disinfecting Sanitizing Wipes can be used for everyone. Ingesting 1-propanol can cause central nervous system (CNS) depression, which can result in death. On June 19, 2020, the U.S. Food and Drug Administration (FDA) advised consumers not to use any hand sanitizer manufactured by "Eskbiochem SA de CV" in Mexico, due to the potential presence of methanol, a "toxic alcohol", as an active ingredient, which can cause blindness and/or death when absorbed through the skin or when swallowed. If soap and water are not readily available, theCenters for Disease Control and Prevention(CDC) recommend consumers use an alcohol-based hand sanitizer that contains at least 60 percent ethanol (also referred to as ethyl alcohol). product voluntarilyrecalledon 11/30/2021, Product labeled to contain methanol; FDA recommended the company recall on 12/6/2021; product voluntarily recalled on 12/6/2021, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality even after receiving a warning letter. 75339-751-02 FDA recommended the company recall on 9/14/2022; product voluntarily recalled lot 1166A on 9/17/2022; FDA issued a warning letter on 12/21/2022. (Florida), Salon Technologies International Sanitizing Hand Spray 80%. 74046-004-03 The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. If You're Using This Hand Sanitizer, Stop Immediately - Best Life Cultivation Republic (Clearwater, Florida). FDA will consider revising the list as appropriate. Picture Information. 71120-112-10 Dongguan Mingyi Medical Products, Co., Ltd. 74721-0002-6 FDA tested product; contains acetaldehyde and acetal contaminants. Product purported to be made at the same facility that produced subpotent ethyl alcohol product;added to import alert to help stop products from entering the U.S. on 12/21/2020; FDA recommended the company recall on 4/12/2021; FDA issued awarning letteron 07/06/2021. 74046-001-14 Consumers who have products on thelist of hand sanitizerswith potential methanol or 1-propanol contamination should immediately stop using the product and dispose of it, ideally in ahazardous waste container. Category: Hand Sanitizer. FDA hand sanitizer recall widens to over 100 products The company recalled one lot of hand sanitizer: Antica Ocean Citron Hand Sanitizer (alcohol) Gel 65%. Health Canada has issued a recall for 19 hand sanitizers because they may pose health risks. Anti-Bac Hand Sanitizer 70% alcohol, Born Basic. Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. The hand sanitizers include brands sold at Sam's Club and BJ's Wholesale Club. 74046-004-09 GSD Advanced Hand Sanitizer Drug Facts Active ingredients Ethyl alcohol 70% v/v Purpose Antimicrobial Use Grapefruit Extract, 74721-0001-1 79279-421-07 74530-015-02 74046-006-02 75293-001-03 74046-001-15 74721-0020-6 74530-011-04 74530-013-03 FDA encourages health care professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAsMedWatch Adverse Event Reportingprogram (please provide the agency with as much information as possible to identify the product): [1/19/2021] Today, FDA issued a guidance outlining the agencys policy for drug manufacturers and compounders to test alcohol or isopropyl alcohol for methanol contamination prior to using the alcohol to produce drugs, including hand sanitizer products. Free shipping. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. Anti-Bac Hand Sanitizer 65% Alcohol, Scent Theory Keep It Clean Pure Clean Anti-bacterial Hand Sanitizer, Cavalry (labeled with Product of Mexico), Natural Gold Gel Alcohol Antiseptic 75% Topical Solution, Command Gel AntiBac Instant hand sanitizer, FDA tested product; contains methanol; FDA recommended the company recall on 7/31/2020; product voluntarily, UltraCruz Hand Sanitizing Gel Antimicrobial, Company tested product; isopropyl alcohol level was subpotent; product voluntarily recalled lot BF12530 on 8/7/2020, Sanit Technologies LLC, doing business as Durisan (Florida), Durisan Antimicrobial Solutions Hand Sanitizer, Alcohol-Free, Company tested product; contains microbial contamination; product, Durisan Antimicrobial Solutions Hand Sanitizing Wipes, Alcohol-Free, New Wave Cleaning Solutions Foaming Hand Sanitizer (Benzalkonium chloride 0.1%), Company tested product; manufacturing process lacks adequate controls to prevent microbial contamination. (Nevada), Mob Liquid Alcohol Antiseptic Hand Sanitizer Non-Sterile Solution, FDA tested product; isopropyl alcohol level was subpotent; FDA recommended the company recall on 10/13/2022, Salon Technologies International Zorin Pharmaceutical Technology Co. Ltd. (China), Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 10/12/2022, Biotipo Pharma Medical Sanitizing Hand Wipes, PalmShield Hand Sanitizer Gel with Aloe and Coconut Oil. Products packaged to appear as drinks, candy or liquor bottles, as well as products marketed as drinks or cocktails because their appearance could result in accidental ingestion or encourage ingestion. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. In a public advisory notice. Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. Consumers who have been exposed to hand sanitizer containing methanol and are experiencing symptoms should seek immediate treatment for potential reversal of toxic effects of methanol poisoning. FDA recommended the company recall on 9/20/2021;product voluntarily recalled on 9/21/2021, SBL Brands LLC dba Global Sanitizers, LLC (Nevada), Hand sanitizer products packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA issued a, Scentsational Soaps and Candles Inc. (Florida), Scentsational Sanitizer Non-Sterile Solution Alcohol Antiseptic 70% Topical Solution, Company tested product; contains methanol, benzene and acetaldehyde; product voluntarily, Fresh Lemon Citron Frais Scented Hand Sanitizer, SS Black and White Collection and Photo Real Collection: Coconut Breeze; Eucalyptus & Mint; Lavender & Herbs; Lemon Zest; Tangerine & Guava, Sck Zeta Dis Ticaret Pazarlama Ltd. (Turkey), FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 1/20/2022; product voluntarily recalled on 1/28/2022. The agency will provide additional information as it becomes available. Updated: Jul 13, 2020 / 11:49 AM PDT. Learn more at poisonhelp.hrsa.gov/. FDA Recalls 149 Hand Sanitizers Due to "Toxic" Methanol - Hand Call 9-1-1 if the person is unconscious or has trouble breathing. In the letter, company asked the FDA to recall the contaminated batches of hand sanitizer, conduct an investigation of the products, and provide information to the public, among other things. GSD Hand Sanitizer, Hand Sanitizer, 33.8 Ounce - amazon.com Recalled hand sanitizers The following products have been recalled as of Aug. 1: ITECH 361's All Clean Hand Sanitizer, Moisturizer and Disinfectant : UPC code 628055370130. Hand sanitizer products packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 09/08/2021. Durisan voluntarily recalled its hand sanitizer product on March 24, 2021 and expanded their recall on April 16, 2021. Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. 33.8 oz. Consult your health care professional if you have used any of these products and have health concerns. It was distributed nationwide to wholesale distributors and retailers. 79279-610-03 Don't drink this: Hand sanitizer recalled over packaging. $ 7.99. Unibeleza Industria E Comercio De 74721-0010-2 Products labeled with harmful or poisonous ingredients, such as methanol. FDA recommends using the test methods described in the USP monograph for alcohol (ethanol) and conducting the testing in a laboratory that has been previously inspected by FDA and is compliant with current good manufacturing practice (CGMP). Recall: Hand Sanitizers May Contain Toxic Methanol - WebMD A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. When the FDA continues to issue recalls for the inclusion of potentially toxic ingredients (as of this release, the list of banned sanitizers has now surpassed 100), we all need a hand sanitizer . FDA issued a, Yara Elena de La Garza Perez Nieto (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 7/10/2020; added manufacturer to, Product labeled to be edible alcohol; added manufacturer to. FDA test results show certain hand sanitizers have concerningly low levels of ethyl alcohol or isopropyl alcohol, which are active ingredients in hand sanitizer products. Valisure . HAN Archive - 00434 | Health Alert Network (HAN) - Centers for Disease 74721-0002-8 The FDA listed the following products in its warning: All-Clean Hand Sanitizer (NDC: 74589-002-01) Esk Biochem Hand Sanitizer (NDC: 74589-007-01) CleanCare NoGerm Advanced Hand Sanitizer 75% . 74046-006-05 79279-521-03 If soap and water are not readily available, the Centers for Disease Control and Prevention (CDC) recommend consumers use an alcohol-based hand sanitizer that contains at least 60 percent ethanol (also referred to as ethyl alcohol). Hand sanitizer recalled over potential methanol contamination Use of this contaminated hand sanitizer by health care professionals who tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization or extend an existing hospitalization. Methanol is not an acceptableingredient for hand sanitizers and must not be used due to its toxic effects. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. $19.95. MIAMI (CBSMiami) - The Food and Drug Administration has added four brands of hand sanitizer to a list of more than 75 that have been recalled. (China). Aloe Vera Based Hand And Skin Purifying Gel. 74046-001-03