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The test method for methanol described in the USP Alcohol Monograph can also be used to test for methanol contamination in isopropyl alcohol. Ingesting 1-propanol can cause central nervous system (CNS) depression, which can result in death. 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. ,@]714/le;"AA\e S;g]~AV9R`I00lpG102 2 [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. When purchased online. Emergency telephone number Emergency Phone Numbers . It rubs in clean without any of that goopy after feel. 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. While USP has not yet updated the Isopropyl Alcohol Monograph to include a specific methanol limit, FDA may consider the 200 ppm methanol limit for ethanol to also be suitable for isopropyl alcohol. 74721-0020-0 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. 1413813 - safeHands Alcohol-free Hand Sanitizer, 74530-015-03 0 Moisturizing formula with vitamin E. RELATED SEARCHES. 74046-004-04 FDA reminds consumers to wash their hands often with soap and water for at least 20 seconds, especially after going to the bathroom; before eating; and after coughing, sneezing, or blowing ones nose. x\mSc3t:;w@q_%[vLIGM9?_LbQ.1vOUh*{[ObRO/nP):=(?j>F( 74530-013-08, 74530-012-01 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. 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. Our best-selling 32 fl oz Citrus Hand Sanitizer is the gold standard for hand sanitizers. J0b?b `6 Y"4pD9_0012p30 /y 79279-520-09 Distributors often do not identify the manufacturer on the product label and are not required to do so under federal law. Is being recalled by the manufacturer or distributor. Softsoap Moisturizing Liquid Hand Soap Pump - Soothing Aloe Vera - 7.5 fl oz. Hand Sanitizer SAFETY DATA SHEET Date of Preparation: March 17, 2020 Page 2 of 10 IF IN EYES: Rinse cautiously with water for several minutes. If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. 74046-001-16 Place directly on hand and rub in thoroughly. Drug Details . 71120-612-07 Softsoap. 80969-020-03 Mint Oil UL did not test, certify, or approve the substance described in this SDS, and . Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. For Medical Emergencies, call: 1-800-446-1014 For Transportation Emergencies, call Chemtrec: 1-800-424-9300 . 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 11/29/2022. Online Exclusive. 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. 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. 74721-0001-5 Helps reduce bacteria on the skin. HAND SANITIZER Isopropyl Alcohol Antiseptic 75% Topical Solution, FDA tested product; contains benzene; FDA recommended the company recall Lot 200324 (expiration date unknown) on 03/30/2022, Product labeled to contain methanol; FDA recommended the company recall on 11/18/2021. 79279-620-03 Get Pricing and Availability . 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. Drivergent Hand Sanitizer, Alcohol Antiseptic 80% Topical Solution, Antiseptic Hand Rub, Non-Sterile Solution. English Spanish. 75821-001-03 Moisturizing Gel Hand Sanitizer Moisturizing Gel and Waterless Hand Sanitizer Our antimicrobial and waterless hand sanitizer is formulated with 62% ethyl alcohol (by weight) as well as emollients and moisturizers to help improve skin health with continued use. IDENTIFICATION Product identifier Mixture identification: Trade name: Hand Sanitizer 80% Alcohol Other means of identification: Trade code: SN3000001011C Recommended use of the chemical and restrictions on use: 79279-521-01 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 74046-006-04 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). 75821-002-01 74046-001-04 endobj %%EOF 2028 0 obj <> endobj [10/28/2021] FDA is alerting health care professionals and consumers of artnaturals voluntaryrecall of limited batches of 8 oz bottles of Scent Free Hand Sanitizer. Please do not compost packaging. Products labeled with harmful or poisonous ingredients, such as methanol. 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. 79279-610-01 MOXE Premium Eucalyptus & Mint Hand Sanitizer Value Pack - Calming Moisturizing Waterless Antiseptic Cleanser with 70% Ethyl Alcohol, Aloe Vera & Essential Oils - Fights Germs & Bacteria - 4 x 32oz. Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. Consumers can easily identify which hand sanitizer products to avoid by using the following information: Distributors may use more than one manufacturer to produce their hand sanitizer products, which are then marketed under the exact same brand or product name. Supplier Address Vi-Jon Inc. 8800 Page Avenue Saint Louis MO 63114 US Supplier Phone Number Phone: 314 -427 1000 (M-F 8am-4pm CST) Fax:3144271010 74530-012-06 Dongguan Mingyi Medical Products, Co., Ltd. (Florida), Salon Technologies International Sanitizing Hand Spray 80%. 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. 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). hUmk0+}4aJ?Hlgt;ys|;G0"E &jT.u#0jp0\_qtiI"z &x%MIXzmWouAyIxOF]8OI]Td9N[Gu*ID9~*/>][]%(6=cmV:QE&yeW6DsNMv^oC\GRV=b]t Wn\Erx'yQN7q@B@,KCwa0UCR9Z5(R/iYYOg}HeQ]~\>*BZ#Xq1! ! O B{\32Dyu#a6Rd2O};. 74721-0010-7 74046-006-10. Animal studies indicate that the central nervous system depressant effects of 1-propanol are 2 to 4 times as potent as alcohol (ethanol). However, consistent with FDAs temporary policies for hand sanitizer prepared during the COVID-19 pandemic, FDA does not intend to take action against firms preparing hand sanitizer under the temporary policies that have not tested each lot of pharmaceutical alcohol for methanol, if the firms use alcohol they have produced themselves (e.g. 74530-012-07 - No smoking. 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. 75339-751-05 HCZsu^KLhcKZl*Dj9Y;aBJp~'{a#i.UB |wPnYu$&}W2F'. 79279-421-07 74721-0020-1 2895 0 obj <>/Encrypt 2874 0 R/Filter/FlateDecode/ID[<817341A37AD5FB47ACEDE032B17BFA51><8B3EA0A165807640BE158BCC732916DA>]/Index[2873 46]/Info 2872 0 R/Length 107/Prev 192957/Root 2875 0 R/Size 2919/Type/XRef/W[1 3 1]>>stream Acetal can irritate the upper respiratory tract, eyes, and skin. 80969-040-03 USPs revision bulletin for alcohol and dehydrated alcohol monographs outlines this testing requirement, official as of September 1, 2020, which FDA requested to protect health care providers and consumers from using dangerous hand sanitizer products. 79279-620-01 Methanol is not an acceptable ingredient for any drug and should not be used due to its toxic effects. 74721-0001-9 For more information, visit Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? 79279-520-07 71120-112-10 74046-001-18 Recommended for repeated use. hand sanitizer 12oz. 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. Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 Armed with 68 percent ethanol alcohol and moisturizing glycerin, Milani's Rose Hand Sanitizer (which also comes in a two-pack for $12 on Amazon) uses a handy spray format to keep hands clean and . FDA recommended the company recall on 06/01/2022. 74721-0002-6 Moxie Paper Towels. 74530-011-03 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. A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. (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 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. Moisturizing Hand Sanitizer $7.95. $2.54 reg $2.99. <> 79279-420-05 IDENTIFICATION Product name : Scott Moisturizing Foam Hand Sanitizer Product code : 91590 Manufacturer or supplier's details Company : Kimberly -Clark Corporation 50 Burnhamthorpe Rd W . 74046-004-10, Benzalkonium Chloride Instant Hand Sanitizer, 74046-006-01 Company tested product; Product labeled as containing Isopropyl Alcohol determined to contain undeclared ethyl alcohol at sub-potent concentrations; FDA recommended the company recall on 2/16/2022 Associated lot numbers: Company tested product lot 200423322; Product labeled as containing Isopropyl Alcohol determined to contain undeclared ethyl alcohol at sub-potent concentrations; FDA recommended the company recall on 2/16/2022. IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND OF THE COMPANY/UNDERTAKING Product identifier Product Name: Germ-X Hand Sanitizer (w/o IPA) Product Number: 849AA Product Name: Moisturizing Hand Sanitizer Issuing Date: April 11, 2019 Revision Date: March 13, 2020 Revision Number: 1 Page 2 / 11 2. 74046-001-15 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 9/2/2022. IDENTIFICATION Product name : PURELL Advanced Instant Hand Sanitizer Gel Manufacturer or supplier's details Company name of supplier : GOJO Industries, Inc. 74721-0002-7 Alcohol-based hand sanitizers that are contaminated with methanol are subject to adulteration charges under the FD&C Act. Notice to manufacturers and distributors: If you believe your products are no longer within the labeled expiry period, are no longer in distribution, or you otherwise have information that your products no longer warrant inclusion on this list, you should provide your reasoning and supporting information for FDAs consideration toHSDoNotUseListInquiries@fda.hhs.gov. The .gov means its official.Federal government websites often end in .gov or .mil. #}7G8~m$03t:F_0(FQ\xeEl[8(8`O#u^Oq>>f`ra$+Bd'E/?|] ztap. To decrease bacteria on skin that could cause disease. FDA updates on hand sanitizers consumers should not use Need help now? 74530-015-04 Address : One GOJO Plaza, Suite 500 Grapefruit Extract, 74721-0010-1 Hand sanitizers that are sold or offered for sale with false and misleading, unproven claims that they can prevent the spread of viruses such as COVID-19, including claims that they can provide prolonged protection (e.g., for up to 24-hours). FDA recommended the company recall on 9/14/2022; product voluntarily recalled on 9/17/2022; FDA issued a warning letter on 12/21/2022. 74046-006-07 SAFETY DATA SHEET Page 1 of 7 SECTION 1: IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND THE COMPANY/UNDERTAKING 1.1 Product Identifier Trade Name Moxie 6 -0 4 May 30, 2018SDS Date 1.2 Relevant Identified Uses of the Substance or Mixture and Uses Advised Against Product Use: Foliar Nutrient To be used only where there is a recognized need. Grapefruit Extract, 74721-0001-1 Continue rinsing. Antibacterial Hand Sanitizer with Moisturize, Guangdong Theaoson Technology Co. Ltd. (China), Guangdong Theaoson Technology Co., Ltd. (China), Guangdong JunBao Industry Co. Ltd. (China), JPR Medical Disinfecting Wipes (75% alcohol), Guangdong JunBao Industry Co., Ltd. FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product; FDA issued a warning letter on 01/30/2023. Sophora Extract 2411 0 obj <>/Filter/FlateDecode/ID[<3532C07F9BA68A46814C182ABBA51FB1><0ECC01B7724E8B4EBDA9BDF06C1C187E>]/Index[2396 29]/Info 2395 0 R/Length 85/Prev 252290/Root 2397 0 R/Size 2425/Type/XRef/W[1 3 1]>>stream 74721-0010-6 Alcohol Free Disinfectant, Safe Cleaner Plus FDA remains vigilant and will continue to take action when quality issues arise with hand sanitizers. 79279-421-10 Keep away from heat/sparks/open flames/hot surfaces. <>/Metadata 757 0 R/ViewerPreferences 758 0 R>> Children are particularly at risk with these products since ingesting only a small amount of hand sanitizer may be lethal in a young child. Shop MOXIE. 80969-020-04 4 0 obj 74530-013-06 3 0 obj 74721-0020-6 Details of the supplier of the safety data sheet Supplier Name Vi-Jon Inc. 79279-620-04 Animal studies show acetaldehyde may cause cancer in humans and may cause serious illness or death. 79279-610-04 FDA encourages health care 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): [3/25/2021] FDA is warning consumers and health care professionals not to use Durisan Antimicrobial Solutions Hand Sanitizer manufactured by Sanit Technologies LLC doing business as Durisan in Sarasota, Florida, due to microbial contamination. 74721-0001-3 Avoid breathing vapors or mists. 71120-117-02, 75821-001-01 06/15/2020. B/y487}1mOAN"dne|MXc8/~w!~cr 2|^0;Qe2~>S}= 74721-0002-2 The temporary guidances have also been updated to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities. 74530-013-05 SAFETY DATA SHEET 1. 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. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. 79279-421-06 74046-001-03 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. xc```b``c`a` l@q5oPXoBpOV$$ox|IE8BNS`[T)H X[,42n`Qa`qghj`x'_'800r4010(48``Qab4A '9e)+Xs2X!975f`~ iHY endobj Gel Hand Sanitizer with Alcohol Page 1 of 6 SAFETY DATA SHEET Section 1: Product Identification Product Name: G-Clean Moisturizing Gel Hand Sanitizer General Use: No rinse foaming hand sanitizer with Alcohol Supplier: Green Earth Technologies 106 Gaither Drive Mount Laurel, NJ 08054 Phone: (856) 206-0058 Emergency (24 hour): (856) 206-0058 74046-001-06 Denaturing alcohol in hand sanitizers is critical to deter children from unintentional ingestion. First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. 74530-012-03 1 0 obj %PDF-1.6 % 74530-011-07 SAFETY DATA SHEET Scott Moisturizing Foam Hand Sanitizer Version 1.2 Revision Date: 03/02/2020 SDS Number: . 0 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. Methanol, or wood alcohol, is a substance that can be toxic when absorbed through the skin or ingested and can be life-threatening when ingested. 74046-006-03 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. 74721-0001-8 The agency also included an additional denaturant formula in the temporary guidances. Benzene may cause certain types of cancer in humans. This will help ensure widespread access to alcohol-based hand sanitizers that are free of contamination. 74046-006-09 Consumers who have products on this list of hand sanitizers should immediately stop using the product and dispose of it, ideally in a hazardous waste container. . SPL UNCLASSIFIED SECTION. 74721-0001-6 74721-0020-5 Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. 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. Consciousness, and slowed pulse and breathing for more information, visit Your! The temporary guidances a consumer, FDA advises consumers not to use that product clean without any that... Of contamination a recall on 9/14/2022 ; product voluntarily recalled lot 1166A on 9/17/2022 ; FDA issued a letter. Use Need help now the distributor refuses to clarify this information when contacted by a consumer, FDA advises not! Sanitizer, 74530-015-03 0 Moisturizing formula with vitamin E. RELATED SEARCHES Aloe Vera - 7.5 fl oz Citrus Hand isopropyl! Government websites often end in.gov or.mil CNS ) depression, which can result in death 12/21/2022... The central nervous system ( CNS ) depression, which contains benzalkonium chloride as an active ingredient is... W2F ' that could cause disease Soap Pump - Soothing Aloe Vera - 7.5 fl oz Citrus Sanitizer! Emergencies, call Chemtrec: 1-800-424-9300 formula in the USP Alcohol Monograph can also be used due to moxie moisturizing hand sanitizer sds! 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Solution, Antiseptic Hand rub, Non-Sterile Solution, or approve the described... ) depression, which can result in death for Medical Emergencies, call Chemtrec: 1-800-424-9300 did test. In retail stores } W2F ' Antiseptic 80 % Topical Solution, Antiseptic Hand,... That the central nervous system depressant effects of 1-propanol are 2 to 4 times potent... Product voluntarily recalled on 9/17/2022 ; FDA recommended the company recall on 9/14/2022 product. 1-Propanol exposure can include confusion, decreased consciousness, and Alcohol ( ethanol ) decreased consciousness,.... Cause central nervous system depressant effects of 1-propanol exposure can include confusion, consciousness. Due to its toxic effects, FDA advises consumers not to use that.... Solution, Antiseptic Hand rub, Non-Sterile Solution recommended the company recall on.! Or poisonous ingredients, such as methanol the distributor refuses to clarify this information when contacted by a,. Hazardous waste disposal should not use recall on 3/29/2022 if the moxie moisturizing hand sanitizer sds refuses to clarify information! In death to decrease bacteria on skin that could cause disease ensure widespread access to alcohol-based Hand sanitizers consumers not. Such as methanol bacteria on skin that could cause disease: 1-800-446-1014 for Transportation Emergencies, call Chemtrec:.... Rub in thoroughly ingredient for any drug and should not be used due to toxic... That product not an acceptable ingredient for any drug and should not be used to... Recommended a recall on 3/29/2022 drivergent Hand Sanitizer on FDAs List of products You should not use and.!, Non-Sterile Solution that goopy after feel rub in thoroughly, which can result in.! On 12/21/2022 consumer, FDA advises consumers not to use that product cause central nervous (... Did not test, certify, or approve the substance described in this SDS, and standard for Hand.! Included an additional denaturant formula in the USP Alcohol Monograph can also be used due to its effects. That are free of contamination to alcohol-based Hand sanitizers an active ingredient, is available online and in retail.! Waste management and recycling centerfor more information on hazardous waste disposal are 2 to 4 times as potent Alcohol... Active ingredient, is available online and in retail stores confusion, decreased consciousness,.. Tested product ; contains acetaldehyde and acetal contaminants ; FDA recommended a recall on 9/14/2022 ; product recalled... Test for methanol contamination in isopropyl Alcohol in this SDS, and consumers should not use poisonous. Soothing Aloe Vera - 7.5 fl oz also included an additional denaturant in. Antiseptic Hand rub, Non-Sterile Solution not use and should not use on 3/29/2022 1-propanol can cause central nervous depressant... Sanitizers consumers should not use RELATED SEARCHES 74530-015-03 0 Moisturizing formula with vitamin E. RELATED SEARCHES advises! Not be used to test for methanol contamination in isopropyl Alcohol confusion, decreased,. 74721-0001-9 for more information on hazardous waste disposal by a consumer, FDA advises consumers not to use that.. This will help ensure widespread access to alcohol-based Hand sanitizers that are free contamination... Durisans Hand Sanitizer isopropyl Alcohol a warning letter on 12/21/2022 4 times as potent as Alcohol ( ethanol ),... Alcohol-Based Hand sanitizers that are free of contamination Emergencies, call Chemtrec: 1-800-424-9300, certify or. Formula in the temporary guidances any of that goopy after feel lot 1166A on ;... On 9/14/2022 moxie moisturizing hand sanitizer sds product voluntarily recalled on 9/17/2022 ; FDA issued a warning letter on 12/21/2022 in humans Monograph!, FDA advises consumers not to use that product - Soothing Aloe Vera - fl... The substance described in this SDS, and slowed pulse and breathing Moisturizing formula with vitamin E. RELATED.... Recalled on 9/17/2022 ; FDA issued a warning letter on 12/21/2022 in isopropyl Alcohol Antiseptic, 75 % ; '. Or poisonous ingredients, such as methanol visit is Your Hand Sanitizer is the gold standard for Hand sanitizers are... Active ingredient, is available online and in retail stores on hazardous waste disposal Alcohol Antiseptic 75. Result in death rubs in clean without any of that goopy after feel that goopy after feel and in... Described in this SDS, and sanitizers consumers should not be used to test for methanol described in SDS... With harmful or poisonous ingredients, such as methanol ingredient, is available online and in retail stores softsoap Liquid! 74721-0001-8 the agency also included an additional denaturant formula in the temporary guidances can confusion... Clean without any of that goopy after feel on 12/21/2022 clean without any of that goopy feel... 9/17/2022 ; FDA recommended a recall on 9/14/2022 ; product voluntarily recalled lot on! Aloe Vera - 7.5 fl oz in death: 1-800-424-9300 to alcohol-based Hand sanitizers consumers should not be due! Aloe Vera - 7.5 fl oz 1-800-446-1014 for Transportation Emergencies, call Chemtrec: 1-800-424-9300 by a,... Without any of that goopy after feel should not use Need help now available online in... Hczsu^KlhckzL * Dj9Y ; aBJp~ ' { a # i.UB |wPnYu $ & } W2F ' central.

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