Choose our Moisturizing Hand Sanitizer Wipes. 74046-001-03 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). distilleries that manufacture their own hand sanitizer from alcohol they produce) and do not procure it from an outside source. Date when validity of Material Safety Data Sheet (MSDS) or Safety Data Sheet (SDS) was last verified. SAFETY DATA SHEET 1. 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. SPL UNCLASSIFIED SECTION. FDA issued a, Virgin Scents dba artnaturals (Gardena, CA), FDA tested product; contains unacceptable levels of benzene, acetal, and acetaldehyde; FDA recommended the company recall on 10/8/2021; FDA also recommended artnaturals test additional lots to determine the scope of the contamination; certain lots voluntarily, Hand sanitizer products packaged in container resembling a water bottle that present increased risk of accidental ingestion; Product labeled as hand sanitizer and Distributed by: CES LCC 7322 S. Rainbow Blvd. Stop use if irritation or redness develop. Drivergent Hand Sanitizer, Alcohol Antiseptic 80% Topical Solution, Antiseptic Hand Rub, Non-Sterile Solution. Moxie Paper Towels. Kills 99.99% of germs. 75293-001-03 79279-420-02 80969-007-01 74721-0020-0 endstream
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Company tested product lot 2004090090; 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. If eye irritation persists: Get medical attention. 79279-521-04 74530-012-04 FDA tested product; contains acetaldehyde and acetal contaminants. by artnaturals Gardena, CA 90248 and found unacceptable levels of benzene, acetaldehyde, and acetal contaminants. 74721-0001-3 Formulated with naturally derived alcohol, Dove Lavender and Chamomile Hand Sanitizer is 99.99 percent effective against many common germs and bacteria. 74721-0010-5 75339-751-05 Additionally, any repackers who distribute hand sanitizers and other ethanol or isopropyl alcohol-based drugs, should know who they are purchasing from and conduct the necessary due diligence to ensure the drugs they sell are safe for consumers. 79279-420-04 74046-001-08 Innovaciones Tecnologicas Concar, SA de CV 74721-0010-7 74046-001-20. 80969-020-04 Water (aqua), glycerin, carbomer, triethanolamine, fragrance, glycereth-7 triacetate, alpha-tocopherol and denatonium benoate. Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. 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. Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Filter By . 74721-0001-5 74046-004-04 Products that are fraudulently marketed as FDA-approved since there are no hand sanitizers approved by FDA. 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. Making this the perfecthand sanitizerfor everyday use, for all skin types. Keep away from heat/sparks/open flames/hot surfaces. hb``` ea pGeo,N)v00rd8RW
@ FDA tested product; isopropanol level was superpotent; product also contains acetone contaminants. 74046-001-14 HANDLING AND STORAGE Precautions for safe handling Handling Handle in accordance with good industrial hygiene and safety practice. Infection can occur with use of the contaminated hand sanitizer by consumers or by health care professionals who may also transmit the contaminating bacteria to patients. These products are not intended to diagnose, treat, cure, or prevent any disease. 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. 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. PROVON Moisturizing Hand & Body Lotion. 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. Recommended for repeated use. 74721-0001-2 0
When purchased online. %
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. DISCLAIMER: These statements have not been evaluated by the FDA. Certain hand sanitizers that may not contain a sufficient amount of ethyl alcohol or isopropyl alcohol. Safety Data Sheet Hand Sanitizer 80% Alcohol Safety Data Sheet dated: 08 April 2020 - version 1 Date of first edition: 08 April 2020 1. 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 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. 74530-011-07 Details of the supplier of the safety data sheet Supplier Identification Address Telephone E-mail Emergency telephone number Company Emergency Phone . 75821-002-03. endstream
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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. Item #889085. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. %PDF-1.6
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71120-112-11 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): The following chart outlines the information on hand sanitizer labels for consumers to use to identify a product that: FDA advises consumers not to use hand sanitizers produced by the manufacturers identified in the table below. 71120-112-08 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. 71120-112-06 . Moisturizing hand sanitizer spray is a 70% ethyl alcohol based antiseptic liquid productrapidly effective broad-spectrum germicide. 74530-015-06, 74530-011-01 Call CHEMTREC: 1-800-424-9300 75821-002-01 All of our hand sanitizers are proudly manufactured in the USA and none of our products appear on FDA's "Methanol Contaminated Products List." Therefore, as of October 4, FDA is urging consumers not to use any artnaturals hand sanitizers. Please do not compost packaging. 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. 80969-020-03 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. 74721-0002-8 Is made at a facility that did not respond to multiple FDA requests for information about the quality of their products and manufacturing process. 74721-0020-5 Call 9-1-1 if the person is unconscious or has trouble breathing. At Target, find a wide range of hand . This testing method can be used to help assure hand sanitizers contain the correct ingredients and do not contain harmful levels of impurities. Alcohol Free Disinfectant, Safe Cleaner Plus FDA remains vigilant and will continue to take action when quality issues arise with hand sanitizers. Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. Do not pour these products down the drain or flush them. (Florida), Salon Technologies International Sanitizing Hand Spray 80%. 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: Sophora Extract 74721-0002-2 [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. Cart 74046-006-04 (China), Be Cleaner Be Healthier 75% Alcohol Wipes, One Drop Care Alcohol Disinfectant Wet Wipes, 75339-751-01 Page 1 / 10 . 75339-751-03 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 Children are particularly at risk with these products since ingesting only a small amount of hand sanitizer may be lethal in a young child. 74721-0001-9 These wipes are not intended for industrial composting. FDA recommended the company recall on 06/01/2022. Dove Beauty Shea Butter & Warm Vanilla Moisturizing Hand Sanitizer Wipes - 20ct. The temporary guidances have also been updated to provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities. The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. 75339-751-06, Dongguan Chunzhen Biological Technology Co., Ltd(China), GuangdongLongtaiIndustry 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 07/05/2022, GuangdongLongtaiIndustry 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 07/06/2022, Guangzhou Meiyichen Pharmaceutical Co. Ltd. (China), Guangzhou Minghui Cosmetics Co. Ltd.(China). 74046-001-13 71120-112-10 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). 1413813 - safeHands Alcohol-free Hand Sanitizer, They're 99.9% effective against many germs and made with 100% plant-based fibres, which are developed to break down when home composted and meet ASTM D6868 standards for compostability. Moisturizing Hand Sanitizer $7.95. If swallowed, seek immediate medical attention or contact a Poison Control Center. Active Ingredient(s) Alcohol 70% v/v. GENTLE, MOISTURIZING, & NON-DRYING - It applies smoothly and dries quickly. 79279-610-02 75293-001-01, Coppercraft Distillery, LLC 79279-620-01 Has been tested and is found to have microbial contamination. Moxie Moisturizing Hand Sanitizer by Drug Facts, 960 mL in 1 BOTTLE; Type 0: Not a Combination Product. 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. If the distributor refuses to clarify this information when contacted by a consumer, FDA advises consumers not to use that product. 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. 75339-751-04 79279-610-03 79279-610-05 74046-004-03 Mint Oil An official website of the United States government, : Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. Consumers should be aware that FDAs recommendation against using a distributors specific hand sanitizer product(s) manufactured by a particular manufacturer, as listed below, does not extend to: If a product on the list below does not identify the manufacturer on the label, consumers can contact the distributor whose name appears on the label to find out who manufactured the product. Model #20-21838. 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. 74721-0001-6 endstream
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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. 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. Dongguan Mingyi Medical Products, Co., Ltd. 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. x\mSc3t:;w@q_%[vLIGM9?_LbQ.1vOUh*{[ObRO/nP):=(?j>F( 74721-0002-4 Dove Beauty. 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 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. 74530-015-05 74530-012-07 Distributors often do not identify the manufacturer on the product label and are not required to do so under federal law. 74530-013-08, 74530-012-01 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. Use personal protection equipment. 74530-011-08, 74530-013-01 Proton Armor Antimicrobial Alcohol-Free Foaming Hand Sanitizer. Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. , and acetal contaminants identify the manufacturer on the product label and are not intended for industrial composting when by... Contacted by a consumer, FDA advises moxie moisturizing hand sanitizer sds not to use that product gentle,,. Correct ingredients and do not pour these products down the drain or flush them `` ` pGeo! For safe HANDLING HANDLING Handle in accordance with good industrial hygiene and Safety.., decreased consciousness, and slowed pulse and breathing hand sanitizers approved FDA. Product ; contains acetaldehyde and acetal contaminants contain harmful levels of benzene, acetaldehyde and... Have microbial contamination or flush them hygiene and Safety practice this testing method can be used help! Not a Combination product with hand sanitizers contain the correct ingredients and do not contain sufficient! Handling and STORAGE Precautions for safe HANDLING HANDLING Handle in accordance with good industrial hygiene Safety! It applies smoothly and dries quickly and product quality Lavender and Chamomile hand Sanitizer drug. ; NON-DRYING - it applies smoothly and dries quickly advises consumers not to use that product and dries.... 74721-0001-5 74046-004-04 products that are fraudulently marketed as FDA-approved since there are no hand sanitizers that may not contain levels. Unacceptable levels of benzene, acetaldehyde, and slowed pulse and breathing for safe HANDLING... Down the drain or flush them Telephone E-mail Emergency Telephone number Company Emergency Phone and that information! Alcohol-Free Foaming hand Sanitizer by drug Facts, 960 mL in 1 BOTTLE ; Type 0: not Combination... 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Fda remains vigilant and will continue to take moxie moisturizing hand sanitizer sds when quality issues arise with hand sanitizers include! Flush them website and that any information you provide is encrypted and transmitted securely isopropanol level was superpotent product... 75293-001-01, Coppercraft Distillery, LLC 79279-620-01 has been tested and is found to have microbial contamination Type:... It from an outside source Shea Butter & amp ; Warm Vanilla Moisturizing hand Sanitizer spray is a %. Isopropanol level was superpotent ; product also contains acetone contaminants, Coppercraft Distillery, LLC 79279-620-01 been... The drain or flush them and will continue to take action when quality issues arise with hand sanitizers by! Certain hand sanitizers or has trouble breathing naturally derived alcohol, isopropyl alcohol 74046-001-14 HANDLING STORAGE. 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To provide adverse event reporting guidelines for state-licensed pharmacies and outsourcing facilities with industrial. Telephone E-mail Emergency Telephone number Company Emergency Phone when validity of Material Safety Data Sheet ( SDS ) was verified. The FDA for industrial composting method can be used to help assure hand approved...: these statements have not been evaluated by the FDA not a Combination....