Label: EAAE HAND SANITIZER- alcohol solution

  • 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 November 2, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    Ethyl Alcohol 62% v/v

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacteria on the skin

  • Warnings

    For external use only.

    Flammable. Keep away from fire or flame

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

  • STOP USE

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away

  • Directions

    • Put enough product on your palm to cover hands and rub hands together briskly untill dry
    • Store below 110F (43C)
  • Inactive ingredients

    Water, Carbomer, Triethanolamine, Glycerin, Aloe barbadensis leaf juice, Tocopheryl acetate

  • 60mL tube

    image description

  • 60mL Bottle

    image description

  • 300ml bottle

    image description

  • 500ml Bottle

    image description

  • INGREDIENTS AND APPEARANCE
    EAAE HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73027-205
    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
    CARBOMER 934 (UNII: Z135WT9208)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73027-205-0160 mL in 1 TUBE; Type 0: Not a Combination Product06/02/2020
    2NDC:73027-205-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    3NDC:73027-205-03300 mL in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    4NDC:73027-205-04500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/02/2020
    Labeler - JIANGSU HANHE DAILY CHEMICALS CO., LTD. (414409758)
    Establishment
    NameAddressID/FEIBusiness Operations
    JIANGSU HANHE DAILY CHEMICALS CO., LTD.414409758manufacture(73027-205)
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!