Label: AOLIBEN DISPOSABLE ALCOHOL DISINFECTANT WIPES cloth

  • 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 February 28, 2022

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

View All Sections
  • DOSAGE & ADMINISTRATION

    Keeping in a closed, shaded, cool and dry place.

  • INACTIVE INGREDIENT

    Purified water,Non-woven fabric

  • INDICATIONS & USAGE

    Tear the outer packaging, take out the cotton piece, and wipe the skin or objects.

  • ACTIVE INGREDIENT

    Alcohol

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    1.This product is disposable and cannot be reused ;
    2.Do not use on eye and lip skin. In case of contact with eyes,rinse with plenty of water ;
    3.Using with caution in persons allergic to alcohol, especially in sensitive skin ;
    4.Please check whether the package is in good condition before use. Do not use if there is any damage ;
    5.This product is insoluble in water, do not dispose of it in the toilet to avoid the toilet is clogged ;
    6.This product is not close to fire sources and high temperature objects ;

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    AOLIBEN DISPOSABLE ALCOHOL DISINFECTANT WIPES 
    aoliben disposable alcohol disinfectant wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56040-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL3 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56040-009-011 in 1 BAG; Type 0: Not a Combination Product09/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/17/2020
    Labeler - Shandong Zhushi Pharmaceutical Group Co., Ltd. (560400484)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shandong Zhushi Pharmaceutical Group Co., Ltd.560400484manufacture(56040-009)
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!