Label: RELIEF HAND SANITIZING WIPE- ethanol 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 June 22, 2020

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

  • Active Ingredient(s)

    Ethanol 62% Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Uses

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Flammable. Keep away from heat and flame.

  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of
    contact with eyes, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of
    a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    ■ Tear open packet. Open and unfold wipe. Thoroughly wipe hands.

    ■ There is a risk of contamination if the wet wipe is put back into

    the packaging with unclean hands.

    ■ Do not throw away wipes in a flush toilet, as there is a risk of clogging it.

    ■ Supervise children under 6 years of age when using this product to avoid

    swallowing.

    ■ Avoid direct inhalation of vapors during application. (Headaches and
    irritation to mucous membranes may occur when directly inhaled.)

    ■ Keep product in its original container as storing the product in anything
    other than the original container may result in accidents or cause the integrity
    of the product to diminish.

  • Other information

    ■ Store between 15-30°C (59-86ºF)

    ■ Avoid freezing and excessive heat above 40°C (104ºF)

  • Inactive ingredients

    Water, Glycerin

  • Package Label - Principal Display Panel

    Relief HAND SANITIZING WIPE

  • INGREDIENTS AND APPEARANCE
    RELIEF HAND SANITIZING WIPE 
    ethanol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79002-062
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79002-062-011 in 1 PACKET; Type 0: Not a Combination Product06/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/22/2020
    Labeler - Daehan P&H Co., Ltd. (557818402)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sauber Co.,Ltd.690395844manufacture(79002-062)