Label: PURELL ADVANCED REFRESHING ALOE- alcohol gel

  • NDC Code(s): 21749-705-01, 21749-705-02, 21749-705-04, 21749-705-08, view more
    21749-705-10, 21749-705-12, 21749-705-20, 21749-705-33, 21749-705-50, 21749-705-80, 21749-705-89
  • 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

  • Uses

    • 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

    • Put enough product in your palm to cover hands and rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using PURELL
  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf 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)

    Distributed by: GOJO Industries, Inc. Akron, OH 44309
    Questions? Tel: 1-888-4-PURELL ■ www.PURELL.com
    ©2011, GOJO Industries, Inc.
    All rights reserved. Made in U.S.A.

  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED REFRESHING ALOE 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-705
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-705-5015 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    2NDC:21749-705-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    3NDC:21749-705-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/201201/01/2022
    4NDC:21749-705-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    5NDC:21749-705-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/201201/01/2022
    6NDC:21749-705-10295 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    7NDC:21749-705-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/201201/01/2022
    8NDC:21749-705-20591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package03/14/201201/01/2022
    9NDC:21749-705-80800 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    10NDC:21749-705-331000 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    11NDC:21749-705-891200 mL in 1 PACKAGE; Type 0: Not a Combination Product03/14/201201/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/14/201201/01/2022
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534MANUFACTURE(21749-705)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414MANUFACTURE(21749-705) , label(21749-705) , pack(21749-705)