Label: 75% ALCOHOL FREE HAND WASHING GEL- hand washing gel gel

  • 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 April 5, 2020

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

View All Sections
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • ACTIVE INGREDIENT

    Ethyl alcoho

  • INACTIVE INGREDIENT

    water、ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER、AMINOMETHYL PROPANOL

  • PURPOSE

    Disinfection

    Sterilization
    No Rinseing

  • INDICATIONS & USAGE

    Uses to decrease bacteria on the skin that could cause disease recommended for repeated use.

    When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin do not inhale oringest

  • WARNINGS

    For external use only:hands

    Stop use and ask a doctor if irritation or redness develops condition persists for more than 72 hours

  • DOSAGE & ADMINISTRATION

    Flammable keep away from fire or flame.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    75% ALCOHOL FREE HAND WASHING GEL 
    hand washing gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55453-001
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL350 mL  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code ekongbell
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55453-001-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/24/2020
    Labeler - Guangzhou Yikang Biotechnology Co., Ltd. (554526730)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yikang Biotechnology Co., Ltd.554526730manufacture(55453-001)
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!