Label: AOLIBEN ZHUSHI HAND SANITIZER GEL- aoliben zhushi hand sanitizergel 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 March 10, 2022

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  • DOSAGE & ADMINISTRATION

    Protect from light, airtight, and moisture. Store in a cool, dry place.

  • INACTIVE INGREDIENT

    Carbomer 980

    Triethanolamine

    Purified water

  • INDICATIONS & USAGE

    1.Sanitary hand :Take a minute to take an appropriate amount of hand sanitizer on the palm of your hand, rub your hands together to coat each part evenly
    2.Surgical hand :After surgical hand washing, take 3-5 minutes to take an appropriate amount of hand disinfectant and evenly apply it to the skin of the hands, forearms and lower thirds of the upper arms.

  • ACTIVE INGREDIENT

    Alcohol

    N-propanol

  • KEEP OUT OF REACH OF CHILDREN

    Topical disinfectants should not be taken orally and should be kept out of reach of children.

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    Flammable, keep away from fire.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    AOLIBEN ZHUSHI HAND SANITIZER GEL 
    aoliben zhushi hand sanitizergel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56040-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL640 mL  in 1000 mL
    PROPYL ALCOHOL (UNII: 96F264O9SV) (PROPYL ALCOHOL - UNII:96F264O9SV) PROPYL ALCOHOL80.36 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56040-007-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/14/2020
    Labeler - Shandong Zhushi Pharmaceutical Group Co., Ltd (560400484)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shandong Zhushi Pharmaceutical Group Co., Ltd560400484manufacture(56040-007)
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