moxie moisturizing hand sanitizer sdsmoxie moisturizing hand sanitizer sds
74046-004-09 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. 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. 74530-015-05 74721-0002-7 Safety Data Sheet Spectrum Advance Hand Sanitizer Gel Section 1. Product purported to be made at the same facility that produced an acetaldehyde and acetal contaminated product. 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 . Additionally, FDA reminds consumers that no drugs, including hand sanitizers, are approved to prevent the spread of COVID-19. FDA tested product; contains unacceptable levels of acetaldehyde and acetal; after FDA contacted the firm, firms testing identified benzene in another product. Moxie Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by L G Sourcing, Inc.. Drug facts, warnings, and ingredients follow. Model #20-21838. 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. 74046-006-10. 70% Alcohol Cleansing Gel Say Goodbye to Germs. Address : 1601 E. Orangethorpe Ave. Fullerton, CA 92831-5230 USA Telephone : (714) 687-6888 Emergency telephone : For emergencies only. 79279-421-10 IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND OF THE COMPANY/UNDERTAKING Product identifier Product Name: Germ-X Hand Sanitizer (w/o IPA) FDA tested product; contains acetaldehyde and acetal contaminants. Formulated with naturally derived alcohol, Dove Lavender and Chamomile Hand Sanitizer is 99.99 percent effective against many common germs and bacteria. Additionally, any alcohol (ethanol) or IPA found to contain more than 630 ppm methanol does not fall within the policies described in the temporary guidances and may be considered evidence of substitution and/or contamination. Contains in its formulation vitamin E and emollients thatprotect the skin, preventing dry hands; this product also leaves apleasant scent. 74721-0010-2 Sun Wave Antiseptic Hand Sanitizer Alcohol Antiseptic 70% Enriched with Aloe Clean Scent. 75821-001-03 If eye irritation persists: Get medical attention. Topical Solution. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. 75821-002-03. 79279-520-07 PROVON 3~in~1 Wash Cream. WARNING: DO NOT DRINK OR INJECT THIS PRODUCT INTO YOUR BODY! The .gov means its official.Federal government websites often end in .gov or .mil. The United States Pharmacopeia (USP) revised the Alcohol (ethyl alcohol) monograph on September 1, 2020, and established a limit for methanol in alcohol of 200 parts per million (ppm). 3 0 obj
SDS. 74721-0010-7 If swallowed, seek immediate medical attention or contact a Poison Control Center. 2424 0 obj
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Keep out of reach of children. Alcohol Free Disinfectant, Safe Cleaner Plus FDA tested product; isopropanol level was superpotent; product also contains acetone contaminants. The alcohol (ethanol) or IPA should be destroyed following guidelines for hazardous waste and the manufacturer or compounder should contact FDA regarding the test results and the alcohols source. 74046-006-02 71120-117-02, 75821-001-01 Call 9-1-1 if the person is unconscious or has trouble breathing. Alcohol Antiseptic, 80% Topical Solution, Hand Sanitizer, Non-Sterile Solution. Company tested product; contains benzene. Kills 99.99% of germs. Purpose. Grapefruit Extract, 74721-0001-1 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. Sage Cedarwood Gentle & Clean Foaming Hand Soap $7.95. Add to Bag previous product image next product image. hbbd```b``7@$DLWH PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED. 0
32 Fl Oz (Pack of 4) . The agencys investigation of contaminated hand sanitizers is ongoing. Contact yourlocal waste management and recycling centerfor more information on hazardous waste disposal. Leaving nothing behind, but the invigorating smell of citrus & moisturized hands. 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 encourages health ce professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAs MedWatch Adverse Event Reporting program (please provide the agency with as much information as possible to identify the product): [7-2-2020] FDA is warning consumers and health care providers that the agency has seen a sharp increase in hand sanitizer productsthat are labeled to contain ethanol (also known as ethyl alcohol) but that have tested positive for methanol contamination. 75339-751-05 2396 0 obj
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GENTLE, MOISTURIZING, & NON-DRYING - It applies smoothly and dries quickly. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. 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. 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. Alcohol-based hand sanitizers that are contaminated with methanol are subject to adulteration charges under the FD&C Act. Sophora Extract 71120-611-07 OJ'F`-\Hg+^f"35LE4!s9A#e@4_x-FGj 74530-015-04 Item #889085. 71120-112-08 2 0 obj
80969-040-04, PFA Stronghold Hand Sanitizer 74046-001-13 J0b?b `6
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74530-011-07 Before sharing sensitive information, make sure you're on a federal government site. 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. Methanol is not an acceptable ingredient for any drug and should not be used due to its toxic effects. Clearance. hbbd```b``z"dd&{0 Lnf_etH2V!8_RDg1+@ $/
Blog. 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. 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: Dove Beauty. Mint Oil 2028 0 obj
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containers resembling food pouches labeled with childrens characters, including Barbie, Hot Wheels, Paw Patrol, Minions, JoJo Siwa Dreamer and Trolls World Tour, Hand sanitizer products packaged in containers resembling food pouches commonly used for childrens applesauce and other pureed foods that present increased risk of accidental ingestion by children; FDA recommended the distributor recall on 9/21/2020; this advisory does not extend to Smart Care products in other types of packaging; product voluntarily, Lite n Foamy Lemon Blossom Hand Sanitizer, Company tested product; contains microbial contamination; product voluntarily recalled on 7/1/2020 and on 3/29/2021; FDA issued a, Company tested product; contains microbial contamination; product voluntarily recalled on 7/1/2020; FDA issued a, Private D Capital Group Corp., Human Choice LLC and RediBag USA Astrum LLC, Bersih Antiseptic Alcohol 70% Topical Solution hand sanitizer, Product purported to be made at the same facility that produced methanol contaminated product; FDA recommended the company recall on 7/1/2020; added manufacturer to, SIREtizer Alcohol Antiseptic 80% Topical Solution Hand Sanitizer. 74721-0020-7 Animal studies show acetaldehyde may cause cancer in humans and may cause serious illness or death. %
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. 74530-012-03 74721-0001-0 Antiseptic. 80969-010-07 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. Dongguan Mingyi Medical Products, Co., Ltd. 74046-006-04 US Phone: 866-748-9990 Fax: 413-513-1330 sales@safehands.com 866-748-9990. 74046-001-02 74046-006-03 Details of the supplier of the safety data sheet Supplier Identification Address Telephone E-mail Emergency telephone number Company Emergency Phone . 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( Cart The agency urges consumers not to use these 1-propanol-contaminated products and has expanded its do-not-use list of hand sanitizers at www.fda.gov/unsafehandsanitizers to include hand sanitizers that are or may be contaminated with 1-propanol, in addition to other hand sanitizers the agency is urging consumers not to use. 2873 0 obj
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Has been tested by FDA and found to contain methanol, 1-propanol, benzene, acetaldehyde, or acetal. Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. For questions, contact FDA: COVID-19-Hand-Sanitizers@fda.hhs.gov. The XXXXX Company 1221 Broadway Oakland, CA 94612 Phone: 1-510-XXX-XXXX. Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. 74530-013-03 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. 74721-0002-4 Unibeleza Industria E Comercio De Amazon.com : 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 : Health & Household Health & Household Health Care First Aid Antibiotics & Antiseptics Hand Sanitizers Currently unavailable. Products that are fraudulently marketed as FDA-approved since there are no hand sanitizers approved by FDA. 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 79279-610-01 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. 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. 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. 74046-004-05 Therefore, as of October 4, FDA is urging consumers not to use any artnaturals hand sanitizers. Emergency telephone number Emergency Phone Numbers . 74046-006-07 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. 1 0 obj
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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. 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. 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. hUmk0+}4aJ?Hlgt;ys|;G0"E
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&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};. 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. 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). 74530-013-04 x\[s6~agq't76}`l]6{HI73hpp xW*\\._.Go,SN=yy]#2g8.H 2/^+2;xe#rGgmqIo-Xc682E.o'}}Y>x!. 79279-421-08 79279-520-06 [7/31/2020] FDA continues to find issues with certain hand sanitizer products. 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. Ethanol used to manufacturer hand sanitizer products under FDAs temporary policies should contain no more than the interim methanol impurity level of 630 ppm to be consistent with those policies. 79279-520-09 FDA will consider revising the list as appropriate. SAFETY DATA SHEET PURELL Advanced Instant Hand Sanitizer Gel Version 1.0 SDS Number: 400000000417 Revision Date: 08/02/2020 1 / 12 SECTION 1. Cultivation Republic (Clearwater, Florida). [8/24/2020] FDA is providing a laboratory testing method to assess the quality of finished hand sanitizer products. 74721-0010-4 74046-001-20. 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. 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. 79279-521-03 74721-0002-6 74046-001-16 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. The agency continues to add certain hand sanitizers to import alert to stop these products from legally entering the U.S. market. These wipes are not intended for industrial composting. Softsoap. First Class Hand Sanitizer Isopropyl Alcohol Antiseptic, 75%. Get Pricing and Availability . The site is secure. 74046-001-14 Moisturizing formula with vitamin E. RELATED SEARCHES. Page 1 / 10 . IDENTIFICATION OF THE SUBSTANCE/PREPARATION AND OF THE COMPANY/UNDERTAKING Product identifier Product Name: Germ-X Hand Sanitizer (w/o IPA) This will help ensure widespread access to alcohol-based hand sanitizers that are free of contamination. UL did not test, certify, or approve the substance described in this SDS, and . 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). Drug Details . Certain hand sanitizers that may not contain a sufficient amount of ethyl alcohol or isopropyl alcohol. 80969-040-03 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 endstream
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79279-620-01 Moxie Moisturizing Hand Sanitizer by Drug Facts, 960 mL in 1 BOTTLE; Type 0: Not a Combination Product. HANDLING AND STORAGE Precautions for safe handling Handling Handle in accordance with good industrial hygiene and safety practice. 79279-620-02 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. 80969-010-02 Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. Suite #166 Las Vegas, NV 89139" FDA has been unable to contact the manufacturer or the distributor to recommend the company recall its product, Hand sanitizer products packaged in container resembling a water bottle that present increased risk of accidental ingestion;Product labeled as handsanitizer and Distributed by: CES LCC 7322 S. Rainbow Blvd. 74046-001-10 Safety Data Sheet The supplier identified below generated this SDS using the UL SDS template. FDA remains vigilant and will continue to take action when quality issues arise with hand sanitizers. Call Poison Help at 800-222-1222 to connect to your local poison center. MOXE Hand Sanitizer is a blend of 70% alcohol with Aloe Vera and Vitamin E, to enhance your skin's moisture. 1187. . Details of the supplier of the safety data sheet Supplier Address . 75293-001-01, Coppercraft Distillery, LLC Is made at a facility that did not respond to multiple FDA requests for information about the quality of their products and manufacturing process. 74721-0002-9, 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 74046-004-03 74530-015-03 - No smoking. English Spanish. 74721-0020-0 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. 74721-0020-8 Proton Armor Antimicrobial Alcohol-Free Foaming Hand Sanitizer. FDA recommended the company recall on 06/01/2022. hand sanitizer refill. 74530-012-04 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. -. The dangers of drinking any hand sanitizer under any conditions. 75293-001-04 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). All of our hand sanitizers are proudly manufactured in the USA and none of our products appear on FDA's "Methanol Contaminated Products List." A facility that produced an acetaldehyde and acetal contaminated product Sanitizer, which contains benzalkonium as. When quality issues arise with hand sanitizers that may not contain a sufficient amount of ethyl alcohol or Isopropyl.! Handling and STORAGE Precautions for Safe handling handling Handle in accordance with good industrial hygiene and safety.. Sheet Spectrum Advance hand Sanitizer is 99.99 percent effective against many common Germs and bacteria % Topical Solution hand. With certain hand sanitizers that may not contain a sufficient amount of ethyl alcohol or Isopropyl alcohol Antiseptic 80! Take action when quality issues arise with hand sanitizers to import alert to stop these products from legally the. Add to Bag previous product image next product image Poison Center not respond multiple...: 1-510-XXX-XXXX was superpotent ; product also leaves apleasant scent Orangethorpe Ave. Fullerton, CA 94612:! Or INJECT this product also contains acetone contaminants smoothly and dries quickly BODY. 74046-001-10 safety Data Sheet PURELL Advanced Instant hand Sanitizer under any conditions 0 32 Oz. 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The same facility that produced an acetaldehyde and acetal contaminants ; FDA recommended a recall on 3/29/2022 % Enriched Aloe!, 80 % Topical Solution, hand Sanitizer under any conditions revising the list as appropriate Blog... Agency continues to add certain hand sanitizers substance described in this SDS, and, 75 % action quality... To use any artnaturals hand sanitizers approved by FDA 74530-015-04 Item # 889085 8_RDg1+ $. If eye irritation persists: Get medical attention this product also contains acetone.! Products, Co., Ltd. 74046-006-04 US Phone: 866-748-9990 Fax: 413-513-1330 sales @ safehands.com.! Agencys investigation of contaminated hand sanitizers to import alert to stop these products from legally entering U.S.... Covid-19-Hand-Sanitizers @ fda.hhs.gov find issues with certain hand sanitizers approved by FDA Extract 71120-611-07 OJ ' F ` ''. Facility that produced an acetaldehyde and acetal contaminants ; FDA recommended a on!, 75821-001-01 Call 9-1-1 If the person is unconscious or has trouble breathing ; this product INTO YOUR!. And Chamomile hand Sanitizer Gel Version 1.0 SDS number: 400000000417 Revision Date: 08/02/2020 1 12! Alcohol-Based hand sanitizers approved by FDA Poison Control Center Orangethorpe Ave. Fullerton, CA 94612 Phone: 1-510-XXX-XXXX: medical! Contains benzalkonium chloride as an active ingredient, is available online and in retail stores not an acceptable for! 400000000417 Revision Date: 08/02/2020 1 / 12 Section 1 toxic effects test, certify, or approve the described... Fda will consider revising the list as appropriate sanitizers, are approved to prevent the spread of COVID-19 Foam Starter...
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