Label: TRAVELSHELD SANITIZING WIPE(70%ALCOHOL)- travelsheld sanitizing wipe 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 November 4, 2020

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

View All Sections
  • ACTIVE INGREDIENT

    Ethyl Alcohol 70%

  • PURPOSE

    Antimicrobial

  • Uses

    To help reduce microbes on the skin

  • Directions

    Apply to hands or skin.
    No rinsing required.Discard after use.

  • WHEN USING

    Avoid contactwith eyes. If contact occurs, rinse thoroughly with water.

  • STOP USE

    irritationor redness develops and lasts.

  • KEEP OUT OF REACH OF CHILDREN

    ln case ofaccidental ingestion,get medical help orcontact a poison control center immediately.

  • INACTIVE INGREDIENT

    Water(Aqua)

  • WARNINGS

    For external use only
    Do not dispose of wipes in flush toilets

    Keep away from fire or flame

  • OTHER SAFETY INFORMATION

    Store below 110°F(43°C)
    May discolor certain fabrics or surfaces

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    TRAVELSHELD SANITIZING WIPE(70%ALCOHOL) 
    travelsheld sanitizing wipe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:96285-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL7 mL  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:96285-001-0120 in 1 BOX11/05/2020
    11 in 1 PACKET
    13.915 mL in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/05/2020
    Labeler - Yangzhou Zhouwan Medical Devices Co.,Ltd (711248001)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yangzhou Zhouwan Medical Devices Co.,Ltd711248001manufacture(96285-001)
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!