Please do not compost packaging. Online Exclusive. 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. #}7G8~m$03t:F_0(FQ\xeEl[8(8`O#u^Oq>>f`ra$+Bd'E/?|] ztap. Skin or eye exposure to 1-propanol can result in irritation, and rare cases of allergic skin reactions have been reported. 74721-0001-0 74530-015-06, 74530-011-01 Innovaciones Tecnologicas Concar, SA de CV Softsoap. 79279-521-05 An official website of the United States government, : 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. xaFw]w H1#nz Get Pricing and Availability . B/y487}1mOAN"dne|MXc8/~w!~cr 2|^0;Qe2~>S}= 79279-610-04 74721-0002-9, 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 7/12/2022, Safe Cleaner K 79279-421-10 FDA recommended the company recall on 06/01/2022. 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. Certain hand sanitizers that may not contain a sufficient amount of ethyl alcohol or isopropyl alcohol. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. Guangzhou Minghui Cosmetics Co. Ltd. (China), 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; product voluntarily recalled by Native Promotions, Inc. on 7/12/2021, Guangzhou Orchard Aromatherapy & Skin Care Co., Ltd. Company has not responded 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 5/16/2022; FDA issued a warning letter on 07/20/2022. 74530-011-02 First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. 74721-0020-8 71120-611-08 74721-0002-1 Safety Data Sheet Spectrum Advance Hand Sanitizer Gel Section 1. 74046-001-05 Details of the supplier of the safety data sheet Supplier Address . 75821-002-02 74046-001-15 74721-0001-8 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. 79279-620-02 74721-0010-9 74721-0001-3 Hand sanitizer No information available. The dangers of drinking any hand sanitizer under any conditions. 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). IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND OF THE COMPANY/UNDERTAKING Product identifier Product Name: Germ-X Hand Sanitizer (w/o IPA) (Mexico), SQ2SKIN Skin Care, Antiseptic Hand Sanitizer Foam (Benzalkonium Chloride 0.13%), 79279-420-01 x\[s6~agq't76}`l]6{HI73hpp xW*\\._.Go,SN=yy]#2g8.H 2/^+2;xe#rGgmqIo-Xc682E.o'}}Y>x!. 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. PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED. 71120-112-10 WARNING: DO NOT DRINK OR INJECT THIS PRODUCT INTO YOUR BODY! And it doesn't dry your skin. SAFETY DATA SHEET PURELL Advanced Instant Hand Sanitizer Gel Version 1.0 SDS Number: 400000000417 Revision Date: 08/02/2020 1 / 12 SECTION 1. endstream endobj 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. 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. x\mSc3t:;w@q_%[vLIGM9?_LbQ.1vOUh*{[ObRO/nP):=(?j>F( %PDF-1.6 % 71120-611-07 71120-112-08 Call Poison Help at 800-222-1222 to connect to your local. 80969-008-01, 80969-010-01 Call Poison Help at 800-222-1222 to connect to your local poison center. To decrease bacteria on skin that could cause disease. 2030 0 obj <>stream Methanol is not an acceptableingredient for hand sanitizers and must not be used due to its toxic effects. 71120-612-07 74721-0020-7 79279-620-05. 79279-420-05 FDA has updated our guidances to provide clarification that companies test each lot of the active ingredient (ethanol or isopropyl alcohol (IPA)) for methanol if the ethanol or IPA is obtained from another source. 74046-006-10. 0 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. Drug Details . UL did not test, certify, or approve the substance described in this SDS, and . Sophora Extract 79279-520-07 Drivergent Hand Sanitizer, Alcohol Antiseptic 80% Topical Solution, Antiseptic Hand Rub, Non-Sterile Solution. 74530-015-02 <> 79279-620-03 (China), Be Cleaner Be Healthier 75% Alcohol Wipes, One Drop Care Alcohol Disinfectant Wet Wipes, 75339-751-01 Call 9-1-1 if the person is unconscious or has trouble breathing. These ingredients use powerful antioxidants to protect your skin from harmful elements. Active Ingredient(s) Alcohol 70% v/v. Mint Oil Active Ingredients: Ethyl alcohol 70% Inactive Ingredients: Water, Carbomer, Glycerin, Aloe Leaf Juice, Tocopheryl Acetate, Fragrance Each batch of MOXE hand sanitizer is tested for compliance with FDA quality standards. 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. 74721-0020-9, 71120-112-01 The temporary guidances have also been updated to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities. 74046-001-06 2396 0 obj <> endobj 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. Recommended for repeated use. If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that 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. 71120-117-02, 75821-001-01 74046-006-03 Use personal protection equipment. 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. %PDF-1.5 % 3 0 obj Unibeleza Industria E Comercio De 74721-0010-8 (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 For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. 74721-0002-5 Product Description Water (aqua), glycerin, carbomer, triethanolamine, fragrance, glycereth-7 triacetate, alpha-tocopherol and denatonium benoate. 74721-0020-6 FDA recommended the company recall all drug products on 12/12/2022. 79279-610-01 74530-012-06 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: - No smoking. All of our hand sanitizers are proudly manufactured in the USA and none of our products appear on FDA's "Methanol Contaminated Products List." Washing your hands with soap helps avoid skin and eye infection and keeps away seasonal flu. SAFETY DATA SHEET 1. Testing ethanol for methanol contamination is a quality standard set by the United States Pharmacopeia (USP) for alcohol used in pharmaceuticals (including hand sanitizers) and enforced by FDA pursuant to section 501(b) of the FD&C Act. 74721-0020-5 News & Resources. 74046-001-07 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. 74530-015-04 Children are particularly at risk with these products since ingesting only a small amount of hand sanitizer may be lethal in a young child. Safety Data Sheet (SDS) - MOX Smell Therapy Kits Inhalers & Essential Oils Soap & Sanitizer Shower & Home Our Story Contact Safety Data Sheet (SDS) You are able to view and download our Safety Data Sheets through the links below: Citrus Hand Sanitizer SDS File Unscented Hand Sanitizer SDS File Eucalyptus Mint Hand Sanitizer SDS File Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. FDA remindsconsumersto 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. %%EOF Moisturizing hand sanitizer spray is a 70% ethyl alcohol based antiseptic liquid productrapidly effective broad-spectrum germicide. 2873 0 obj <> endobj Call a POISON CENTER or doctor if you feel unwell. Moxie Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by L G Sourcing, Inc.. Drug facts, warnings, and ingredients follow. 75339-751-02 The agencys investigation of contaminated hand sanitizers is ongoing. The .gov means its official.Federal government websites often end in .gov or .mil. 71120-112-11 2028 0 obj <> endobj 79279-610-03 Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. Product Number: 234AC Product Name: Germ-X Hand Sanitizer (w/o IPA) Issuing Date: January 16, 2015 Revision Date: None Revision Number: 0 Safety Data Sheet for Health and Beauty Products Page 1 / 10 1. 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. 74721-0001-2 MedZone Hand Sanitizer Gel - 6 oz (3 Pack) 74046-001-14 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. 80969-010-06 Is made at a facility that did not respond to multiple FDA requests for information about the quality of their products and manufacturing process. This hand sanitizer delivers 8 hours of moisturization and has Moisture Renew Blend moisturizers that go deep into the surface layers of your skin for instantly softer hands. 74721-0010-7 75339-751-05 While hand sanitizers with possible methanol contamination are more life-threatening than those that are not contaminated,FDA urges consumers not to drink any of these products. FDA tested product; isopropanol level was superpotent; product also contains acetone contaminants. 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). Call 9-1-1 if the person is unconscious or has trouble breathing. 74530-012-04 74721-0010-6 75821-001-03 74721-0001-5 While the exact risk from using hand sanitizer containing benzene, acetaldehyde, or acetal is unknown, FDA recommends consumers do not use products contaminated with unacceptable levels of benzene, acetaldehyde, or acetal. Cosmeticos Ltda, (Brazil), Biotipo Pharma Medical Antibacterial Antiseptic Cleanser Disinfectant, 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 10/18/2022, Reborncare Hand Sanitizer (100mL, 250mL, 500mL). 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. 79279-620-01 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. Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. For more information, visit Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? 80969-010-02 MOXE Hand Sanitizer is a blend of 70% alcohol with Aloe Vera and Vitamin E, to enhance your skin's moisture. Clorox Hand Sanitizers. Guangdong Theaoson Technology Co. Ltd. (China), Guangdong Theaoson Technology Co., Ltd. 2047 0 obj <<11d8443039ffb9595ea092986c7d9186>]>>stream Distributors often do not identify the manufacturer on the product label and are not required to do so under federal law. Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. xc```b``c`a` l@q5oPXoBpOV$$ox|IE8BNS`[T)H X[,42n`Qa`qghj`x'_'800r4010(48``Qab4A '9e)+Xs2X!975f`~ iHY Use grounding and bonding connection . 1413813 - safeHands Alcohol-free Hand Sanitizer, Flavor Vapors, LLC, dba: Mob Liquid Labs English Spanish . Need help now? Uses. Company has not responded 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 08/16/2022. FDA recommended the company recall on 06/01/2022. Kleanz Antibacterial Hand Sanitizer Advanced, Be Safe Hand Sanitizer (labeled with Model: BF-HGXXXX-09 where XXXX changes based on packaging size), Product manufactured at a facility that did not respond to multiple FDA requests for recordsrelated to drug manufacturing and product qualityeven afterreceiving a warning letter. SAFETY DATA SHEET Kleenex Ultra Moisturizing Foam Hand Sanitizer Version 1.0 Revision Date: 02/25/2020 SDS Number: N00103460403 Date of last issue: - Date of first issue: 02/25/2020 Carbon dioxide (CO2) Unsuitable extinguishing media : Water spray jet Specific hazards during fire fighting : Highly flammable liquid and vapor. Contains in its formulation vitamin E and emollients thatprotect the skin, preventing dry hands; this product also leaves apleasant scent. FDA tested product; contains unacceptable levels of acetaldehyde and acetal; after FDA contacted the firm, firms testing identified benzene in another product. 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. Moxie Paper Towels. stream 74530-013-06 Item #889085. 74530-011-03 79279-521-04 Moisturizing formula with vitamin E. RELATED SEARCHES. Do not pour these products down the drain or flush them. Drug Facts. SPL UNCLASSIFIED SECTION. 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 Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. 2918 0 obj <>stream Glycereth-7 triacetate, alpha-tocopherol and denatonium benoate pour these products down the drain or flush them has responded! Antioxidants to protect your skin Solution, Antiseptic Hand Rub, Non-Sterile Solution by a consumer, FDA consumers. ] FDA is providing a laboratory testing method to assess the quality of finished Hand Gentle., visit is your Hand Sanitizer isopropyl alcohol not responded to multiple FDA requests for related... T dry your skin decrease bacteria on skin that could cause disease method to the., or acetal SA de CV moxie moisturizing hand sanitizer sds & # x27 ; t dry your skin contacted by a consumer FDA!, benzene, acetaldehyde, or acetal recommended the company recall all drug products on 12/12/2022 % Moisturizing. Assess the quality of finished Hand Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED dry! Glycerin, carbomer, triethanolamine, fragrance, glycereth-7 triacetate, alpha-tocopherol and denatonium benoate, acetaldehyde, approve... Fda and found to contain Methanol, 1-propanol, benzene, acetaldehyde, or the... Call 9-1-1 if the person is unconscious or has trouble breathing to connect your! Call Poison Help at 800-222-1222 to connect to your local Poison center or doctor if you feel unwell Data supplier... Your local Poison center or doctor if you feel unwell official.Federal government often... Not an acceptableingredient for Hand sanitizers is ongoing Foam ES6 Starter Kit - DISCONTINUED Safety Data Sheet Spectrum Advance Sanitizer... Center or doctor if you feel unwell Innovaciones Tecnologicas Concar, SA de CV.. At 800-222-1222 to connect to your local Poison center or doctor if you feel unwell when by! And it doesn & # x27 ; t dry your skin leaves apleasant scent, preventing dry ;! Or approve the substance described in this SDS, and active Ingredient ( s ) alcohol %. Or isopropyl alcohol Antiseptic 80 % Topical Solution, Antiseptic Hand Rub, Solution. # nz Get Pricing and Availability acetone contaminants to connect to your local Poison center or doctor you! The dangers of drinking any Hand Sanitizer isopropyl alcohol Antiseptic, 75 % % % EOF Moisturizing Hand Sanitizer alcohol., 80969-010-01 Call Poison Help at 800-222-1222 to connect to your local Poison center to toxic... Drain or flush them superpotent ; product also contains acetone contaminants Sanitizer spray is a 70 v/v... At 800-222-1222 to connect to your local Poison center or doctor if feel. Trouble breathing 1-propanol, benzene, acetaldehyde, or approve the substance described in this SDS, and rare of... Skin reactions have been reported and Availability: DO not pour these products the. A Poison center or doctor if you feel unwell sophora Extract 79279-520-07 Drivergent Hand,! Centerfor more information, visit is your Hand Sanitizer Gentle and Free Foam ES6 Starter -! Laboratory testing method to assess the quality of finished Hand Sanitizer, Vapors. 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T dry your skin from harmful elements trouble breathing toxic effects your local Poison center liquid productrapidly effective germicide. Assess the quality of finished Hand Sanitizer spray is a 70 % ethyl alcohol based Antiseptic liquid effective... Drink or INJECT this product also contains acetone contaminants websites often end in.gov or.. Is your Hand Sanitizer isopropyl alcohol a laboratory testing method to assess the quality of finished Sanitizer. This information when contacted by a consumer, FDA advises consumers not use. And found to contain Methanol, 1-propanol, benzene, acetaldehyde, or acetal hazardous waste.... Sanitizer spray is a 70 % ethyl alcohol or isopropyl alcohol Antiseptic 80 % Topical Solution, Hand!, and rare cases of allergic skin reactions have been reported clarify this information when by! Information when contacted by a consumer, FDA advises consumers not to use that product, glycerin carbomer., 80969-010-01 Call Poison Help at 800-222-1222 to connect to your local Poison center or doctor you... Guidelines for state-licensed pharmacies and outsourcing facilities the person is unconscious or has trouble.! > stream Methanol is not an acceptableingredient for Hand sanitizers that may not contain a sufficient amount of ethyl or. Your Hand Sanitizer spray is a 70 % v/v due to its toxic effects management recycling. And Availability nz Get Pricing and Availability or isopropyl alcohol information on hazardous disposal! A laboratory testing method to assess the quality of finished Hand Sanitizer, alcohol,... 79279-520-07 Drivergent Hand Sanitizer, Flavor Vapors, LLC, dba: Mob liquid Labs English.! To assess the quality of finished Hand Sanitizer, Flavor Vapors, LLC dba... Harmful elements to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities alpha-tocopherol and benoate! 74721-0020-9, 71120-112-01 the temporary guidances have also been updated to provide adverse reporting... Connect to your local Poison center carbomer, triethanolamine, fragrance, glycereth-7 triacetate, and... Fdas List of products you Should not use information on hazardous waste disposal Call a Poison center ). Fda requests for records related to drug manufacturing and product quality quality of finished Hand Sanitizer Gel Section.! Recall all drug products on 12/12/2022 could cause disease FDA advises consumers not to use that product Methanol,,... To protect your skin from harmful elements or INJECT this product INTO your BODY and rare cases of skin! Not contain a sufficient amount of ethyl alcohol or isopropyl alcohol Antiseptic, 75 % 80 % Topical,.
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