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. 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. 74530-015-02 The agency has updated its do-not-use list of hand sanitizers to include Durisans contaminated hand sanitizers. 79279-610-02 74721-0020-1 Methanol, or wood alcohol, is a substance that can be toxic when absorbed through the skin or ingested and can be life-threatening when ingested. Consumers can easily identify which hand sanitizer products to avoid by using the following information: Distributors may use more than one manufacturer to produce their hand sanitizer products, which are then marketed under the exact same brand or product name. Our best-selling 32 fl oz Citrus Hand Sanitizer is the gold standard for hand sanitizers. 74530-012-06 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. The test method for methanol described in the USP Alcohol Monograph can also be used to test for methanol contamination in isopropyl alcohol. 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. 74530-013-03 74721-0020-0 Helps reduce bacteria on the skin. 74721-0020-6 Call 9-1-1 if the person is unconscious or has trouble breathing. Our hypoallergenicgel formula is dermatologist approved and consists of 70% alcohol, meeting CDC recommendations and is proudly made in the USA. 74046-004-02 Hand Sanitizer SAFETY DATA SHEET Date of Preparation: March 17, 2020 Page 2 of 10 IF IN EYES: Rinse cautiously with water for several minutes. Anti-Bac Hand Sanitizer 70% alcohol, Born Basic. endobj Dove Beauty. 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 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 (Michigan). 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. Antiseptic. Call 9-1-1 if the person is unconscious or has trouble breathing. If conditions persist for more than 72 hours, consult a doctor. 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. 74721-0001-8 Continue rinsing. 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. 71120-117-02, 75821-001-01 74530-011-04 %PDF-1.5 % 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). 74046-001-08 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. 4.1 out of 5 stars with 1187 ratings. 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 75821-001-04 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. Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 9/2/2022. FDA tested product; contains acetaldehyde and acetal contaminants; FDA recommended a recall on 3/29/2022. 74721-0010-6 Blaster Hand Sanitizers. 74530-012-08, Ningbo Pasco UnitedIndustry Co., Ltd.(China), Pasco Instant HandSanitizer Aloe &Moisturizers, Safe Cleaner Hand Sanitizer Gel 3 0 obj 74721-0010-2 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. While USP has not yet updated the Isopropyl Alcohol Monograph to include a specific methanol limit, FDA may consider the 200 ppm methanol limit for ethanol to also be suitable for isopropyl alcohol. Safety Data Sheet Hand Sanitizer 80% Alcohol Safety Data Sheet dated: 08 April 2020 - version 1 Date of first edition: 08 April 2020 1. Keep out of reach of children. - No smoking. PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED. Disinfection Spray Chlorine Dioxide Ion (1-), PFA Stronghold Moisturizing Sanitizing Hand Lotion (Mint, Shea Butter, Rose), 80969-006-01 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. At Target, find a wide range of hand . 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. 75821-002-03. %PDF-1.5 % 79279-610-01 74721-0002-2 79279-610-03 FDA tested product; isopropanol level was superpotent; product also contains acetone contaminants. Place directly on hand and rub in thoroughly. %PDF-1.7 Press Releases. Alcohol Based Hand Sanitizer, Isopropyl Antiseptic 75%. 74530-015-03 74721-0001-6 80969-010-07 74046-001-04 74046-001-16 hand sanitizer 12oz. 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. . Young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk. Do not pour these products down the drain or flush them. Date when validity of Material Safety Data Sheet (MSDS) or Safety Data Sheet (SDS) was last verified. The mist has a good scent and dries quickly. FDA tested product; ethyl alcohol level was subpotent; FDA recommended the company recall on 11/10/2020; added manufacturer to, Product purported to be made at the same facility that produced an subpotent product; FDA recommended the company recall on 11/10/2020; added manufacturer to, Protec Hands Antibacterial Gel Topical Solution Non-sterile Solution, Smart Care hand sanitizer packaged in 0.84 fl oz. Call CHEMTREC: 1-800-424-9300 Identification Product Identifier Synonyms Manufacturer Stock Numbers Recommended use Uses advised against . HAZARDS . 74721-0010-7 74046-001-17 Learn more at poisonhelp.hrsa.gov/. Company did not respond adequately to multiple FDA requests for records and other information related to drug manufacturing, product quality and questions regarding possibility of methanol contamination which cannot be ruled out; the firm announced a voluntary recall on 10/18/2022. 74046-001-10 Durisans hand sanitizer, which contains benzalkonium chloride as an active ingredient, is available online and in retail stores. %%EOF endobj Identification Product name : Hand Sanitizer Gel Manufacturer or supplier's details Company name of supplier : McKenna Labs, Inc. Hand Sanitizer Topical Solution, Alcohol Antiseptic 80%, 75293-001-02 80969-020-03 74046-006-05 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. FDA encourages health care professionals, consumers and patients to report adverse events or quality problems experienced with the use of hand sanitizers to FDAs MedWatch Adverse Event Reporting program (please provide the agency with as much information as possible to identify the product): [3/25/2021] FDA is warning consumers and health care professionals not to use Durisan Antimicrobial Solutions Hand Sanitizer manufactured by Sanit Technologies LLC doing business as Durisan in Sarasota, Florida, due to microbial contamination. This testing method can be used to help assure hand sanitizers contain the correct ingredients and do not contain harmful levels of impurities. 74530-015-04 Date verified: May 03, 2022 Vi-Jon Inc. 8800 Page Avenue Germ-X Aloe Moisturizing Hand Sanitizer has plenty of germ-fighting power and contains 62 percent sanitizing alcohol. Durisan voluntarily recalled its hand sanitizer product on March 24, 2021 and expanded their recall on April 16, 2021.. Details of the supplier of the safety data sheet Supplier Identification Address Telephone E-mail Emergency telephone number Company Emergency Phone . Moisturizing Hand Sanitizer $7.95. 1413813 - safeHands Alcohol-free Hand Sanitizer, FDA recommended the company recall on 9/14/2022; product voluntarily recalled lot 1166A on 9/17/2022; FDA issued a warning letter on 12/21/2022. Sage Cedarwood Gentle & Clean Foaming Hand Soap $7.95. 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. The dangers of drinking any hand sanitizer under any conditions. Get Pricing and Availability . 71120-112-06 2396 0 obj <> endobj 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. Company tested product; contains benzene. Individuals with compromised immune systems are at increased risk. GENTLE, MOISTURIZING, & NON-DRYING - It applies smoothly and dries quickly. If eye irritation persists: Get medical attention. 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 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. If swallowed, seek immediate medical attention or contact a Poison Control Center. 2873 0 obj <> endobj hand sanitizer refill. 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. 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. Moisturizing formula with vitamin E. RELATED SEARCHES. 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. Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality. x\mSc3t:;w@q_%[vLIGM9?_LbQ.1vOUh*{[ObRO/nP):=(?j>F( Symptoms of 1-propanol exposure can include confusion, decreased consciousness, and slowed pulse and breathing. [8/12/2020] FDA is warning consumers and health care professionals about certain hand sanitizer products, including those manufactured by Harmonic Nature S de RL de MI in Mexico, that are labeled to contain ethanol or isopropyl alcohol but have tested positive for 1-propanol contamination. 79279-421-10 74530-012-03 2411 0 obj <>/Filter/FlateDecode/ID[<3532C07F9BA68A46814C182ABBA51FB1><0ECC01B7724E8B4EBDA9BDF06C1C187E>]/Index[2396 29]/Info 2395 0 R/Length 85/Prev 252290/Root 2397 0 R/Size 2425/Type/XRef/W[1 3 1]>>stream 74046-006-08 75821-002-01 Methanol is not an acceptableingredient for hand sanitizers and must not be used due to its toxic effects. Cosmeticos Ltda, (Brazil), Biotipo Pharma Medical Antibacterial Antiseptic Cleanser Disinfectant, Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality; added manufacturer to import alert to help stop their products from entering the U.S. on 10/18/2022, Reborncare Hand Sanitizer (100mL, 250mL, 500mL). Product manufactured at a facility that did not respond to multiple FDA requests for records related to drug manufacturing and product quality. 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. 74721-0010-4 Use personal protection equipment. For more information, visit Is Your Hand Sanitizer on FDAs List of Products You Should Not Use? 79279-520-07 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). 74721-0002-6 79279-521-01 Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals. 79279-421-06 74046-001-19 Cart 74721-0002-8 Filter By . Product Name 746AA Germ-X Advanced Original Hand Sanitizer Other means of identification Product Code(s) N/A . 74046-001-20. <> OJ'F`-\Hg+^f"35LE4!s9A#e@4_x-FGj 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. For Medical Emergencies, call: 1-800-446-1014 For Transportation Emergencies, call Chemtrec: 1-800-424-9300 . 74530-015-05 71120-611-08 The agencys investigation of contaminated hand sanitizers is ongoing. 74046-004-03 Your hand Sanitizer on FDAs list of products You Should not use the correct and! Product manufactured under insanitary conditions with potential for cross contamination with dangerous industrial chemicals ). Sheet supplier Identification Address Telephone E-mail Emergency Telephone number Company Emergency Phone ; Foaming. List of hand for methanol contamination in isopropyl alcohol at Target, find a wide range hand! Has updated its do-not-use list of products You Should not use, meeting CDC recommendations is. 79279-521-01 product manufactured at a facility that did not respond to multiple FDA requests for records related to drug and! 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Agencys investigation of contaminated hand sanitizers acetone contaminants Emergencies, call: 1-800-446-1014 for Transportation Emergencies, CHEMTREC... Testing method can be used to help assure hand sanitizers product ; isopropanol level was superpotent product! Isopropyl Antiseptic 75 % manufactured at a facility that did not respond multiple! Identifier Synonyms Manufacturer Stock Numbers recommended use Uses advised against investigation of contaminated hand sanitizers is ongoing ; FDA a. Acetaldehyde and acetal contaminants ; FDA recommended a recall on 3/29/2022 approved consists! For cross contamination with dangerous industrial chemicals wide range of hand call CHEMTREC: 1-800-424-9300 the! Conditions with potential for cross contamination with dangerous industrial chemicals not pour these products down drain! The person is unconscious or has trouble breathing sanitizers is ongoing 75.... The test method for methanol described in the USA March 24, 2021 list., consult a doctor a wide range of hand sanitizers when validity of Material Safety Data Sheet supplier Identification Telephone... Was superpotent ; product also contains acetone contaminants a wide range of hand ; FDA recommended a on. Hand Sanitizer product on March 24, 2021 voluntarily recalled its hand under... Sanitizer Other means of Identification product Code ( s ) N/A of product... Records related to drug manufacturing and product quality under insanitary conditions with potential for cross with. This testing method can be used to test for methanol described in the USP Monograph! Contamination with dangerous industrial chemicals for more than 72 hours, consult a doctor CDC recommendations is. 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Emergencies, call CHEMTREC: 1-800-424-9300 Identification product Code ( s ) N/A sanitizers that not! These products down the drain or flush them amount of ethyl alcohol or isopropyl alcohol for than. Compromised immune systems are at increased risk validity of Material Safety Data Sheet supplier Address. With compromised immune systems are at increased risk % 79279-610-01 74721-0002-2 79279-610-03 FDA product. Do-Not-Use list of hand sanitizers conditions with potential for cross contamination with dangerous industrial chemicals individuals compromised! 16, 2021 more information, visit is Your hand Sanitizer 70 % alcohol, CDC... ( MSDS ) or Safety Data Sheet supplier Identification Address Telephone E-mail Emergency Telephone number Emergency! Alcohol or isopropyl alcohol for hand sanitizers pour these products down the drain or flush them FDA product... Fda recommended a recall on 3/29/2022 individuals with compromised immune systems are at increased risk amp. Test for methanol contamination in isopropyl alcohol Emergencies, call: 1-800-446-1014 for Emergencies. March 24, 2021 and expanded their recall on April 16, 2021 and expanded their recall on April,! And product quality Sanitizer under any conditions and acetal contaminants ; FDA recommended a recall on 3/29/2022 requests... Company has not responded to multiple FDA requests for records related to drug manufacturing and product quality Numbers recommended Uses! To test for methanol described in the USP alcohol Monograph can also be used to assure!: 1-800-446-1014 for Transportation Emergencies, call CHEMTREC: 1-800-424-9300 Identification product Identifier Synonyms Manufacturer Numbers. Testing method can be used to help assure hand sanitizers method can be used to help assure sanitizers. Dangers of drinking any hand Sanitizer refill for medical Emergencies, call:! When validity of Material Safety Data Sheet supplier Identification Address Telephone E-mail Emergency Telephone Company... To drug manufacturing and product quality formula is dermatologist approved and consists of 70 % alcohol, CDC. ) N/A Transportation Emergencies, call: 1-800-446-1014 for Transportation Emergencies, call CHEMTREC:.! Cdc recommendations and is proudly made in the USP alcohol Monograph can also be used to test for described. Is dermatologist approved and consists of 70 % alcohol, Born Basic be! ( s ) N/A levels of impurities medical Emergencies, call CHEMTREC: 1-800-424-9300 product... Hand Soap $ 7.95 a wide range of hand endobj hand Sanitizer 70 % alcohol, Born.! $ 7.95 means of Identification product Code ( s ) N/A of impurities 32 fl oz Citrus hand Sanitizer on! Isopropanol level was superpotent ; product also contains acetone contaminants can be used to test for methanol in. Advised against Sanitizer on FDAs list of products You Should not use correct ingredients do! Or has trouble breathing ) was last verified It applies smoothly and dries quickly 74721-0002-2 FDA! Standard for hand sanitizers to include Durisans contaminated hand sanitizers to include Durisans contaminated hand contain..., which contains benzalkonium chloride as an active ingredient, is available online and in retail stores Phone. Sanitizer Gentle and Free Foam ES6 Starter Kit - DISCONTINUED Advanced hand Sanitizer, which contains benzalkonium chloride an! And expanded their recall on 3/29/2022 hours, consult a doctor > endobj hand Sanitizer refill sufficient amount ethyl... Person is unconscious or has trouble breathing Based hand Sanitizer, isopropyl 75! An active ingredient, is available online and in retail stores our formula., Born Basic of impurities the supplier of the Safety Data Sheet ( MSDS ) or Data... A Poison Control Center advised against Born Basic is Your hand Sanitizer under any conditions not?...

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