Label: CO-PROTECT HAND SANITIZERGEL- hand sanitizergel 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 August 24, 2020

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

View All Sections
  • DOSAGE & ADMINISTRATION

    1.Store between 15-30°C(59-86°F).
    2.Avoid freezing and excessive heat above 40°C(104°F).

  • INACTIVE INGREDIENT

    Water, Carbomer, Triethanolamine, Dimethylamine, Aloe Barbadensis Leaf Juice

  • INDICATIONS & USAGE

    Place enough product on hands to cover all sufaces.Rub hands together until dry.

  • ACTIVE INGREDIENT

    Ethyl Alcohol

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. lf swallowed get medical help or contact a Poison Control Center right away.

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    For external use only. Flammable.Keep away from heat or flame

  • PRINCIPAL DISPLAY PANEL

    0201

  • INGREDIENTS AND APPEARANCE
    CO-PROTECT HAND SANITIZERGEL 
    hand sanitizergel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41500-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL1.05 mL  in 1.5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    DIMETHYLAMINE (UNII: ARQ8157E0Q)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41500-010-011.5 mL in 1 VIAL; Type 0: Not a Combination Product08/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/25/2020
    Labeler - Beijing Runyi Technology Co., Ltd (415008922)
    Establishment
    NameAddressID/FEIBusiness Operations
    Beijing Runyi Technology Co., Ltd415008922manufacture(41500-010)
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!