Label: WEITEER HAND SANITIZING GEL- hand sanitizer 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 June 7, 2020

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  • DOSAGE & ADMINISTRATION

    Protect from light and store in a cool, dry and ventilated place.

  • INACTIVE INGREDIENT

    Water,Glycerin,CarbomerU20,Triethanolamine,PhenoXyaethanolum,Sorbitol,essence,1,2-Propanediol

  • INDICATIONS & USAGE

    Apply this product evenly to the hands 1-2 times, the action time is 1 minute

  • ACTIVE INGREDIENT

    Ethyl Alcohol

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    1. This product is a disinfectant for external use and should not be taken orally. Place in a place where the amount of children is not easily accessible.
    2. This product contains alcohol, keep away from open fire.
    3. For those who are allergic to alcohol, those with allergies should be used with caution.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    WEITEER HAND SANITIZING GEL 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55868-001
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL375 mL  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    METHYL BENZOATE (UNII: 6618K1VJ9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55868-001-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/05/2020
    Labeler - Jiangsu Druchor Biological Technology Co., Ltd. (554534924)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangsu Druchor Biological Technology Co., Ltd.554534924manufacture(55868-001)
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