Label: ON GUARD SANITIZING WIPES- alcohol 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 January 31, 2022

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  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    •Decreases bacteria on hands [skin].
    •Recommended for repeated use.

  • Warnings

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

  • WHEN USING

    Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

    Stop use and ask a doctor if irritation or rash appears and lasts.

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

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs and lasts.

  • 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

    Wet hands thoroughly with wipe and allow to dry without rinsing. Throw away after use. Do not flush.

  • Other information

    • Store at a temperature below 38 C (100 F).
  • Inactive ingredients

    Water (Aqua), Eucalyptus globulus Leaf Oil, Citrus aurantium dulcis (Orange) Peel Oil, Eugenia caryophyllus (Clove) Bud Oil, Glycerin, Cinnamomum zeylanicum Leaf Oil, Cinnamomum zeylanicum Bark Oil, Rosmarinus officinalis (Rosemary) Leaf/Stem Oil,
    Aloe barbadensis Leaf Extract.

  • Package Label - Principal Display Panel

    20 Count NDC: 71630-199-20 20 Count Box Label

    Single Packet: NDC 71630-199-11 Single Packet

  • INGREDIENTS AND APPEARANCE
    ON GUARD SANITIZING WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71630-199
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CINNAMON LEAF OIL (UNII: S92U8SQ71V)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    CLOVE OIL (UNII: 578389D6D0)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71630-199-201400 mL in 1 CARTON; Type 0: Not a Combination Product09/23/2020
    2NDC:71630-199-1170 mL in 1 PACKET; Type 0: Not a Combination Product09/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/23/2020
    Labeler - doTERRA International, LLC (832274935)
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