Label: PURELL HAND SANITIZING WIPES ALCOHOL FORMULA- alcohol cloth

  • NDC Code(s): 21749-367-24, 21749-367-36, 21749-367-63, 21749-367-68, view more
    21749-367-76, 21749-367-94
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 25, 2020

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  • Active ingredient

    Ethyl alcohol 62%

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacteria on the skin

  • Warnings

    Flammable. Keep away from fire or flame. For external use only

    When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts 

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Wet hands thoroughly with product and allow to dry

    • Children under 6 years of age should be supervised when using PURELL® products

  • Other information

    • Store below 110°F (43°C)

    • May discolor certain fabrics or surfaces

  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL HAND SANITIZING WIPES ALCOHOL FORMULA 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-367
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CORN OIL (UNII: 8470G57WFM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-367-761 in 1 PACKAGE02/24/201212/31/2019
    11.97 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:21749-367-2424 in 1 PACKAGE02/24/201212/31/2019
    266 mL in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:21749-367-3636 in 1 PACKAGE02/24/2012
    3101 mL in 1 PACKAGE; Type 0: Not a Combination Product
    4NDC:21749-367-6380 in 1 PACKAGE02/24/2012
    4219 mL in 1 CANISTER; Type 0: Not a Combination Product
    5NDC:21749-367-94135 in 1 PACKAGE02/24/201212/31/2019
    5370 mL in 1 PACKAGE; Type 0: Not a Combination Product
    6NDC:21749-367-68175 in 1 PACKAGE02/24/2012
    6479 mL in 1 CANISTER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/24/2012
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-367)
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