Label: ALCOHOL WIPES cloth

  • 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 May 18, 2020

If you are a consumer or patient please visit this version.

View All Sections
  • DOSAGE & ADMINISTRATION

    Please use it as soon as possible after opening Place it in a cool and dry place

  • INACTIVE INGREDIENT

    Glycerin，Aloe Extract, Polyurethane, Non-woven Fabric，Water

  • INDICATIONS & USAGE

    Open the package, pull out a paper towel, wipe back and forth between palms

  • ACTIVE INGREDIENT

    Alcohol

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    Alcohol is volatile ,Please use it as soon as possible after opening Place it in a cool and dry place, avoid direct sunlight and fire,and avoid children eating by mistake Please keep out of the reach of children, Avoid contact with eyes and damaged skin.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPES 
    alcohol wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54237-013
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL100 mL  in 20 
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYURETHANE-34 (40 MPA, TENSILE STRENGTH OF FILM AT BREAK) (UNII: 77KA3O6NNF)  
    WATER (UNII: 059QF0KO0R)  
    ALOE (UNII: V5VD430YW9)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code Ecfinest
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54237-013-0120 in 1 PACKET; Type 0: Not a Combination Product05/18/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/18/2020
    Labeler - Guangzhou Daieme Cosmetic Co,.Ltd (542359812)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Daieme Cosmetic Co,.Ltd542359812manufacture(54237-013)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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