Label: RISUA CLEAN HAND SANITIZER ETHANOL- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

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 28, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredients 

    Active ingredients: ALCOHOL 70.00%

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Water, Glycerin, Carbomer, Triethanolamine, Aloe barbadensis leaf juice, Coix Lacryma-jobi ma-yuen seed extract, Morus bombycis root extract

  • Purpose

    Purpose: SANITIZER

  • Warnings

    Warnings:

    Flammable. Keep away from fire or flame.
    For external use only
    Stop use and ask a doctor if irritation of redness develops and persist
    Keep out of reach of children
    In case of accidental digestion, seek professional assistance or contact a poison control center immediately

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. 

  • Uses

    Uses:

    To help remove bacteria and germs on the skin

  • Directions

    Directions:

    Please enough product in palm to cover hands and rub hands together briskly until dry.
    Not recommended for infants.

  • Other information

    Other information
    Store between 20-23℃(68-74℉)
    When possible, do not store above 40℃(104℉)

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of pouch

  • INGREDIENTS AND APPEARANCE
    RISUA CLEAN HAND SANITIZER ETHANOL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73758-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70.0 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73758-030-011.5 mL in 1 POUCH; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/01/2020
    Labeler - Dasol Co.,ltd. (557839013)
    Registrant - Dasol Co.,ltd. (557839013)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dasol Co.,ltd.557839013manufacture(73758-030)
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

More Info on this Drug

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