Label: BRIGHT SCIENCE HAND SANITIZING WIPES- 80% alcohol v/v 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 February 3, 2021

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

  • ACTIVE INGREDIENT

    Alcohol 80% v/v

  • PURPOSE

    Antimicrobial

  • WARNINGS

    Flammable. Keep away from heat or flame. For external use only. Do not take internally. Do not use in or near eyes.

  • ASK DOCTOR

    Stop use and ask a doctor if irritation and redness develop.

  • STOP USE

    Stop use and ask a doctor if condition persists or gets worse

  • WHEN USING

    When using this product , do not get into eyes or mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • INDICATIONS & USAGE


    • To sanitize hands, completely moisten all hand surfaces and allow to air dry. Responsibly dispose of used wipes.
    • Supervise children under 6 years of age when using this product.

  • OTHER SAFETY INFORMATION


    • Do not apply internally. Keep canister tightly closed and at controlled room temperature. Hold away from face when opening.

  • INACTIVE INGREDIENT

    water, glycerin, hydrogen peroxide

  • DOSAGE & ADMINISTRATION

    Use at least one wipe to thoroughly wet skin surfaces where antimicrobial activity is desired. Do not apply to or around eyes or mouth.

  • PRINCIPAL DISPLAY PANEL

    80 WET WIPES NDC 77093-401-0180 wet wipes NDC: 77093-401-01

  • BRIGHT SCIENCE SANITIZING HAND WIPES, LS29W, NDC77093-401-01

  • INGREDIENTS AND APPEARANCE
    BRIGHT SCIENCE HAND SANITIZING WIPES 
    80% alcohol v/v cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77093-401
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 100 mL
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL  in 100 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77093-401-0180 in 1 CANISTER03/15/2021
    1515 mL in 1 CANISTER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/03/2021
    Labeler - Vincit Zee (097763525)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vincit Zee097763525manufacture(77093-401)