Label: PURELL ADVANCED WITH ALOE INSTANT HAND SANITIZER- alcohol liquid

  • NDC Code(s): 21749-703-04, 21749-703-10, 21749-703-12, 21749-703-20, view more
    21749-703-80, 21749-703-89
  • 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 January 1, 2022

If you are a consumer or patient please visit this version.

  • Active ingredient

    Ethyl alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacterial on the skin that could cause disease

  • WARNINGS

    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

    Place enough product in your palm to thoroughly cover your hands
    Rub hands together briskly until dry
    Children under 6 years of age should be supervised when using this product.

  • Inactive ingredients

    Water (Aqua), Isoproyl Alcohol, Aloe Barbadensis Lead Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)

  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED WITH ALOE INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-703
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.70 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Glycerin (UNII: PDC6A3C0OX)  
    Isopropyl Myristate (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    Caprylyl Glycol (UNII: 00YIU5438U)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-703-101000 mL in 1 PACKAGE; Type 0: Not a Combination Product05/05/201101/01/2022
    2NDC:21749-703-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product05/05/201101/01/2022
    3NDC:21749-703-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
    4NDC:21749-703-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
    5NDC:21749-703-80800 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
    6NDC:21749-703-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product05/05/201101/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/05/201101/01/2022
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-703)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-703) , label(21749-703) , pack(21749-703)