Label: PURELL ADVANCED SOOTHING- alcohol gel

  • NDC Code(s): 21749-713-01, 21749-713-02, 21749-713-04, 21749-713-08, view more
    21749-713-10, 21749-713-12, 21749-713-20, 21749-713-24, 21749-713-27, 21749-713-28, 21749-713-33, 21749-713-40, 21749-713-65, 21749-713-67
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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

View All Sections
  • 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 Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED SOOTHING 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-713
    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:21749-713-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/201802/28/2023
    2NDC:21749-713-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
    3NDC:21749-713-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
    4NDC:21749-713-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
    5NDC:21749-713-10295 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
    6NDC:21749-713-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
    7NDC:21749-713-20591 mL in 1 PACKAGE; Type 1: Convenience Kit of Co-Package11/01/201803/31/2023
    8NDC:21749-713-27800 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/201807/31/2022
    9NDC:21749-713-28826 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/201809/30/2021
    10NDC:21749-713-331000 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/2018
    11NDC:21749-713-401200 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/201803/31/2023
    12NDC:21749-713-672000 mL in 1 PACKAGE; Type 0: Not a Combination Product11/01/201807/31/2021
    13NDC:21749-713-65192 mL in 1 PACKAGE; Type 0: Not a Combination Product07/01/2021
    14NDC:21749-713-24710 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/01/2018
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-713)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-713) , label(21749-713) , pack(21749-713)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!