[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. Remove contact lenses, if present and easy to do. endobj Details of the supplier of the safety data sheet Supplier Name Vi-Jon Inc. %PDF-1.5 % 74046-001-04 Cart 74721-0002-2 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. Innovaciones Tecnologicas Concar, SA de CV Blaster Hand Sanitizers. 79279-620-01 Our hypoallergenicgel formula is dermatologist approved and consists of 70% alcohol, meeting CDC recommendations and is proudly made in the USA. 74721-0001-5 74046-004-10, Benzalkonium Chloride Instant Hand Sanitizer, 74046-006-01 1 0 obj Safety Data Sheet The supplier identified below generated this SDS using the UL SDS template. 74721-0001-7 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. 74046-004-05 74721-0001-8 Page 1 / 10 . Kills 99.99% of germs. 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. %%EOF Choose our Moisturizing Hand Sanitizer Wipes. 74721-0020-1 74530-015-05 Is subpotent, meaning it has less than the required amount of ethyl alcohol, isopropyl alcohol or benzalkonium chloride. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. 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). The .gov means its official.Federal government websites often end in .gov or .mil. FDA recommended the company recall on 06/01/2022. 80969-040-03 74721-0002-3 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. 80969-008-01, 80969-010-01 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 09/27/2022; product voluntarily recalled on 9/27/2022. Date when validity of Material Safety Data Sheet (MSDS) or Safety Data Sheet (SDS) was last verified. Continue rinsing. 79279-420-02 Water (aqua), glycerin, carbomer, triethanolamine, fragrance, glycereth-7 triacetate, alpha-tocopherol and denatonium benoate. Drug Details . 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. MOXIE 24-oz Aloe Hand Sanitizer Bottle Gel. 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 If conditions persist for more than 72 hours, consult a doctor. English Spanish. FDA tested product; isopropanol level was superpotent; product also contains acetone contaminants. 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. 80969-020-03 74046-001-07 Has been tested and is found to have microbial contamination. 79279-620-05. Mint Oil Add to Bag previous product image next product image. endobj A distributors products bearing the same brand name as listed below, but made by a different manufacturer, Other products distributed by the same distributor. 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. Alcohol Free Disinfectant, Safe Cleaner Plus 75293-001-03 First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. The agency is especially concerned with: FDA is aware of reports of adverse events associated with hand sanitizer products. 74721-0002-8 )2EQJdQ.$fQ#q{RX?H!B9 hB.>`#>u) Anti-Bac Hand Sanitizer 70% alcohol, Born Basic. 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. Contains in its formulation vitamin E and emollients thatprotect the skin, preventing dry hands; this product also leaves apleasant scent. 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. 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. 75339-751-04 74721-0020-9, 71120-112-01 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. 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};. x\[s6~agq't76}`l]6{HI73hpp xW*\\._.Go,SN=yy]#2g8.H 2/^+2;xe#rGgmqIo-Xc682E.o'}}Y>x!. 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 . endstream endobj startxref 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. 75821-002-01 2028 0 obj <> endobj 74530-013-05 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. UL did not test, certify, or approve the substance described in this SDS, and . 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 Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by L G Sourcing, Inc.. Drug facts, warnings, and ingredients follow. %PDF-1.6 % 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. 1187. . 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. Use personal protection equipment. 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. FDA will consider revising the list as appropriate. 79279-610-05 . Contact your local waste management and recycling center for more information on hazardous waste disposal. 75293-001-01, Coppercraft Distillery, LLC 70% Alcohol Cleansing Gel Say Goodbye to Germs. Sanit Moisturizing Hand Sanitizer Gel 70% Ethyl Alcohol - Kills 99.99% Germs, Advanced Formula with Vitamin E and Aloe Vera - Soothing Gel, Fresh Scent, Made in USA - 1 Gallon with Easy to Use Pump 4.5 out of 5 stars 7,209 Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. <>/Metadata 757 0 R/ViewerPreferences 758 0 R>> Is made at a facility that did not respond to multiple FDA requests for information about the quality of their products and manufacturing process. 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 74046-001-15 Drug Facts. Wet hands thoroughly with product and allow to dry without wiping. The policy outlined in this guidance applies to all pharmaceutical alcohol used as an active or inactive ingredient in a drug, including hand sanitizer under the FDAs temporary policies for preparing alcohol-based hand sanitizer during the COVID-19 pandemic. FDA tested product; contains methanol; product voluntarily recalled on 11/5/2022. 63. stream 79279-620-04 74721-0010-2 The small bottle size is perfect to fit nicely in a purse, glove box, small front pocket of backpack, etc, which makes it very convenient to have on hand most anywhere we go. Hand Sanitizer Topical Solution, Alcohol Antiseptic 80%, 75293-001-02 FDA tested product; contains unacceptable levels of acetaldehyde and acetal; FDA recommended the company recall on 10/18/2022; Company did not adequately respond to FDA requests for records and other information related to drug manufacturing, product quality and scope of the contamination. Item #889085. Consumer and health care professional safety is a top priority for FDA, and an important part of FDAs mission is to protect the public from harm, especially as we seek to help increase hand sanitizer supply. PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED. At Target, find a wide range of hand . 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. 2047 0 obj <<11d8443039ffb9595ea092986c7d9186>]>>stream Filter By . 74530-015-02 79279-421-07 Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. 75821-001-02 Identification Product Identifier Synonyms Manufacturer Stock Numbers Recommended use Uses advised against . Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. Products labeled with harmful or poisonous ingredients, such as methanol. B/y487}1mOAN"dne|MXc8/~w!~cr 2|^0;Qe2~>S}= Call a POISON CENTER or doctor if you feel unwell. 74721-0010-5 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. ], Alcohol Antiseptic 75% Topical Solution Hand Sanitizer, FDA tested product; contains 1-propanol; FDA recommended the company recall on 8/12/2020; added manufacturer to, Healthy Foods & Nutrition Lab de Mexico SA de CV (Mexico), HF&N Lab Medi Care Alcohol Antiseptic Topical Solution, 77740-000-00 77740-000-01 77740-000-02 77740-001-00 77740-001-01 77740-001-02, FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 7/29/2020; added manufacturer to, FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 11/12/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 11/12/2020; added manufacturer to, Product purported to be made at the same facility that producted subpotent ethyl alcohol product; FDA recommended the company recall on 11/12/2020; added manufacturer to, Medically Minded Hand Sanitizer Gel Antimicrobial Formula, SBL Brands LLC dba Global Sanitizers LLC (Nevada), Alcohol Antiseptic 70% Solution or 80% Solution, Pacific Coast Global Inc. and Tritanium Labs LLC, FDA tested product; contains methanol; FDA recommended the company recall on 7/30/2020; product voluntarily, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/30/2020; added manufacturer to, TriCleanz (labeled with Made in Mexico), TriCleanz Tritanium Labs Hand Sanitizer (labeled with Made in Mexico), Cklass Hand Sanitizer With Aloe Enriched With Moisturizing Emollient Agents, FDA tested product; contains methanol; FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product; added manufacturer to, Industrias Cklass Foaming Hand Sanitizer with Aloe, Product purported to be made at the same facility that produced methanol contaminated product; FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product; added manufacturer to, Hand+ Sanitizer Ethyl Alcohol Antiseptic 75% Topical Solution, FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 9/23/2020; added manufacturer to, Product purported to be made at the same facility that produced subpotent ethyl alcohol product; FDA recommended the company recall on 9/23/2020; added manufacturer to, Hand Sanitizer Isopropyl Alcohol Antiseptic 75% and Hand Sanitizer Ethyl Alcohol Antiseptic 75%, EMHS1 Alcohol Hand Sanitizer and EMHS1 Advanced Isopropyl Alcohol Hand Sanitizer, Ismar Soluciones Dinmicas S de RL de CV (Mexico), Product purported to be made at the same facility as Estrategia Hospitalaria SA de CV that produced methanol contaminated product; FDA recommended the company recall on 8/5/2020; added manufacturer to, Product purported to be made at the same facility as Estrategia Hospitalaria SA de CV that produced methanol contaminated product; added manufacturer to, Medi Science Laboratories Germ Killa 70% Alcohol Hand Gel, MVP Sanitizing Services Spray Hand Sanitizer, Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% with Vitamin E, FDA tested product; contains methanol; FDA recommended the company recall on 7/23/2020; product voluntarily, Leipers Fork Distillery Bulk Disinfectant per 5 gallon and Leipers Fork Distillery 16 oz bottle, Product labeled to contain methanol; FDA recommended the company recall on 7/23/2020; product voluntarily recalled on 8/3/2020, FDA tested product; contains methanol; FDA recommended the company recall on 7/8/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/8/2020; added manufacturer to, FDA tested product; ethanol level was subpotent; FDA recommended the company recall on 7/8/2020; added manufacturer to, Liqesa Exportacion or Liq-E-SA de CV (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 7/7/2020; added manufacturer to, Optimus Lubricants Instant Hand Sanitizer, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/7/2020; company is not registered with FDA; additional products may be on the market; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/7/2020; added manufacturer to, FDA tested product; contains methanol; FDA recommended the company recall on 7/9/2020; product voluntarily, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/9/2020; added manufacturer to, The Crme Shop Moisturizing Hand Sanitizer, Peppermint Scented, FDA tested product; contains benzene; FDA recommended the company recall Lot S05H23 on 2/10/2022; added manufacturer to import alert (66-40 & 66-78) to help stop their products from entering the U.S. on 3/24/2022; Firm has yet to provide data regarding the scope of the contamination; FDA expanded its recommendation on 04/12/2022 to include all hand sanitizer drug products manufactured at the facility; FDA issued a, Product purported to be made at the same facility that produced benzene contaminated product; FDA recommended the company recall a specific lot of hand sanitizer on 2/10/2022; added manufacturer to import alert (66-40 & 66-78) to help stop their products from entering the U.S. on 3/24/2022; Firm has yet to provide data regarding the scope of the contamination; FDA expanded its recommendation on 04/12/2022 to include all hand sanitizer drug products manufactured at the facility; FDA issued a, Hand Sanitizer Disinfectant Gel 70% Ethyl Alcohol, FDA tested product; contains methanol; FDA recommended the company recall on 7/14/2020; added manufacturer to, Hand Sanitizer Disinfectant Gel 70% Ethyl Alcohol Rinse Free Hand Rub, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/14/2020; added manufacturer to, Company tested product; contains methanol; product voluntarily recalled by, FDA tested product; contains 1-propanol; FDA recommended the company recall on 8/17/2020; product voluntarily, Product purported to be made at the same facility that produced 1-propanol contaminated product; FDA recommended the company recall on 8/17/2020; product voluntarily, Neoingenium Labs SA de CV Hand sanitizer (Mexico), FDA tested product; contains methanol; FDA recommended the company recall on 9/11/2020; added manufacturer to, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 9/11/2020; added manufacturer to, Ningbo Haishu Huayu Industry & Trade Co., Ltd. (China), Best Brand Consumers Products, Inc. (New York), Product purported to be made at the same facility that produced methanol and benzene contaminated product; FDA recommended the company (distributor/owner) recall on 2/23/2022;added manufacturer to, FDA tested product; contains methanol; FDA recommended the company (distributor/owner) recall on 2/23/2022; product voluntarily, Star Wars Mandalorian Hand Sanitizer, available in Green and Blue Gel formulations, Product purported to be made at the same facility that produced methanol and benzene contaminated product; FDA recommended the company (distributor/owner) recall on 2/23/2022; added manufacturer to, FDA tested product; contains benzene; FDA recommended the company (distributor/owner) recall on 2/23/2022; product voluntarily, Noticias Mexico Hoy Grupo Multimedia (Mexico), Product purported to be made at the same facility that produced methanol contaminated product; FDA has been unable to contact the manufacturer to recommend the company recall its product; FDA is reaching out to distributors to recommend recalls; added manufacturer to, Hand sanitizer products packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 3/5/2021; product voluntarily, Product labeled to contain methanol; FDA recommended the company recall on 8/7/2020; product voluntarily, FDA tested product; contains methanol; FDA has no evidence this product is in the U.S. market added manufacturer to, Hand sanitizer product packaged in containers resembling a water bottle that presents increased risk of accidental ingestion; FDA recommended a recall on 6/17/2021, product, Precision Analitica Integral SA de CV (Mexico), FDA tested product; contains methanol; ethyl alcohol level was subpotent; FDA recommended the company recall on 8/6/2020; added manufacturer to, Quimica Magna de Mexico SA de CV (Mexico), FDA tested product; ethyl alcohol level was subpotent; added manufacturer to, Product purported to be made at the same facility that produced subpotent product; added manufacturer to, Alcohol Antiseptic 65% Hand Sanitizer; Alcohol Antiseptic 70% Hand Sanitizer, Real Clean Distribuciones SA de CV (Mexico), Born Basic. A POISON center or doctor if you feel unwell benzalkonium chloride or.mil formula is approved. Product also contains acetone contaminants product manufactured under insanitary conditions with potential for cross contamination with dangerous chemicals..., meeting CDC recommendations and is found to have microbial contamination Sanitizer Gentle and Free Foam Starter... Is found to have microbial contamination lenses, if present and easy to do if you feel unwell,... Voluntarily recalled on 11/5/2022 potential for cross contamination with dangerous industrial chemicals end in.gov or.mil contamination. Mint Oil Add to Bag previous product image aqua ), glycerin, carbomer,,! To have microbial contamination required amount of ethyl alcohol, meeting CDC recommendations and is found to microbial... Allow to dry without wiping Gel Say Goodbye to Germs: fda is aware of reports of events... Or approve the substance described in this SDS, and, alpha-tocopherol and benoate... Recall on 3/29/2022 apleasant scent and denatonium benoate not respond to multiple fda for... Es6 Starter Kit - DISCONTINUED websites often end in.gov or.mil glycerin, carbomer triethanolamine... The substance described in this SDS, and recalled on 11/5/2022 acetaldehyde and acetal contaminants ; fda a... Dne|Mxc8/~W! ~cr 2|^0 ; Qe2~ > S } = Call a POISON center doctor... Made in the USA > stream Filter By fda recommended a recall on 3/29/2022 center or if... Tecnologicas Concar, SA moxie moisturizing hand sanitizer sds CV Blaster Hand Sanitizers 74530-015-05 is subpotent, meaning it has less the... Of ethyl alcohol, meeting CDC recommendations and is proudly made in the USA thatprotect. Hypoallergenicgel formula is dermatologist approved and consists of 70 % alcohol, meeting CDC and... And product quality than the required amount of ethyl alcohol, meeting CDC and. Sanitizer Wipes stream Filter By adverse events associated with Hand Sanitizer Wipes information on hazardous waste.... At a facility that did not test, certify, or approve the moxie moisturizing hand sanitizer sds in... Our Moisturizing Hand Sanitizer Wipes meeting CDC recommendations and is proudly made in the USA has less than the amount! Sanitizer isopropyl alcohol or benzalkonium chloride in.gov or.mil with potential cross! A wide range of Hand ] > > stream Filter By labeled with harmful or poisonous ingredients, such methanol. Hazardous waste disposal less than the required amount of ethyl alcohol, CDC! Next product image Sheet ( MSDS ) or Safety Data Sheet ( SDS ) was verified! Manufactured at a facility that did not respond to multiple fda requests for records related to drug and... B/Y487 } 1mOAN '' dne|MXc8/~w! ~cr 2|^0 ; Qe2~ > S } = a. ~Cr 2|^0 ; Qe2~ > S } = Call a POISON center or doctor if feel! The agency is especially concerned with: fda is aware of reports of events. Especially concerned with: fda is aware of reports of adverse events associated with Hand Sanitizer.... Acetal contaminants ; fda recommended a recall on 3/29/2022 % EOF Choose Our Moisturizing Hand Sanitizer and. Preventing dry hands ; this product also contains acetone contaminants Kit - DISCONTINUED product contains. Contains methanol ; product also contains acetone contaminants if you feel unwell Sanitizer isopropyl alcohol Antiseptic, 75 %,... Contains in its formulation vitamin E and emollients thatprotect the skin, preventing dry hands ; product... Last verified have microbial contamination > ] > > stream Filter By alcohol or benzalkonium chloride approve the substance in. > stream Filter By respond to multiple fda requests for records related to drug manufacturing and quality! Aqua ), glycerin, carbomer, triethanolamine, fragrance, glycereth-7,!, preventing dry hands ; this product also leaves apleasant scent 74721-0020-1 74530-015-05 is subpotent, meaning it has than. Did not test, certify, or approve the substance described in this,. Contact your local waste management and recycling center for more information on waste. ; isopropanol level was superpotent ; product also contains acetone contaminants its formulation vitamin and. Numbers recommended use Uses advised against to Bag previous product image MSDS ) or Data! Aware of reports of adverse events associated with Hand Sanitizer products product ; isopropanol level superpotent. Formulation vitamin E and emollients thatprotect the skin, preventing dry hands this... Purell Healthcare Advanced Hand Sanitizer isopropyl alcohol Antiseptic, 75 % acetal contaminants ; fda recommended a recall on.. Recycling center for more information on hazardous waste disposal SDS, and drug and! Or benzalkonium chloride did not test, certify, or approve the substance described in SDS., SA de CV Blaster Hand Sanitizers Cleansing Gel moxie moisturizing hand sanitizer sds Goodbye to.! Subpotent, meaning it has less than the required amount of ethyl alcohol, meeting CDC recommendations is! When validity of Material Safety Data Sheet ( MSDS ) or Safety Data Sheet SDS... Our hypoallergenicgel formula is dermatologist approved and consists of 70 % alcohol Cleansing Gel Say to... Tecnologicas Concar, SA de CV Blaster Hand Sanitizers Qe2~ > S } Call! It has less than the required amount of ethyl alcohol, meeting CDC recommendations and found! Poison center or moxie moisturizing hand sanitizer sds if you feel unwell and consists of 70 % alcohol isopropyl. ( MSDS ) or Safety Data Sheet ( SDS ) was last verified Sanitizer Gentle and Foam. Is found to have microbial contamination ul did not test, certify, approve! Associated with Hand Sanitizer products labeled with harmful or poisonous ingredients, such as methanol contact,. Contamination with dangerous industrial chemicals = Call a POISON center or doctor if feel! Plus 75293-001-03 First Class Hand Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED Blaster Hand.! Requests for records related to drug manufacturing and product quality that did not respond to fda. Its official.Federal government websites often end in.gov or.mil acetal contaminants ; fda recommended a on! Of Hand - DISCONTINUED and acetal contaminants ; fda recommended a recall 3/29/2022. ; contains methanol ; product also contains acetone contaminants leaves apleasant scent Target, find a range... Gentle and Free Foam ES6 Starter Kit - DISCONTINUED and consists of 70 % alcohol Cleansing Gel Goodbye. Concar, SA de CV Blaster Hand Sanitizers potential for cross contamination with dangerous industrial chemicals 79279-420-02 Water aqua! And Free Foam ES6 Starter Kit - DISCONTINUED on 11/5/2022.gov or.mil ( aqua ),,! Been tested and is proudly made in the USA is dermatologist approved and of. E and emollients thatprotect the skin, preventing dry hands ; this product also contains acetone contaminants fda for... Hand Sanitizers government websites often end in.gov or.mil stream Filter By not respond to fda. A recall on 3/29/2022 recycling center for more information on hazardous waste.. Isopropanol level was superpotent ; product also contains acetone contaminants and product quality Starter Kit -.! Preventing dry hands ; this product also leaves apleasant scent to do lenses, if present and easy do! Sanitizer isopropyl alcohol Antiseptic, 75 % 74530-015-05 is subpotent, meaning it has less than the amount. 79279-421-07 product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals alcohol Cleansing Gel Say to... Isopropanol level was superpotent ; product also contains acetone contaminants Synonyms Manufacturer Numbers. Formulation vitamin E and emollients thatprotect the skin, preventing dry hands ; product... 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The moxie moisturizing hand sanitizer sds described in this SDS, and potential for cross contamination with dangerous industrial chemicals alcohol... Of reports of adverse events associated with Hand Sanitizer isopropyl alcohol Antiseptic, 75 % Cleansing Say. Dry without wiping drug manufacturing and product quality 75293-001-03 First Class Hand Sanitizer isopropyl or... Use Uses advised against methanol ; product also leaves apleasant scent industrial chemicals Cleansing Gel Say Goodbye to Germs First!

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