Label: ON GUARD SANITIZING GEL- alcohol gel

  • NDC Code(s): 71630-098-50
  • Packager: doTERRA International, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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

  • ACTIVE INGREDIENT

    Active ingredient Purpose
    Ethyl Alcohol 70% v/v ......................... Antiseptic

  • Antiseptic, Hand Sanitizer

    Antiseptic, Hand Sanitizer

  • Uses

    Uses
    • Reduces bacteria on hands[skin]
    • Recommended for repeated use

  • Warnings

    Warnings
    Flammable. Keep away from flame, spark, or
    temperatures above 40°C (104°F)
    For external use only.

  • WHEN USING

    When using this product avoid contact with eyes. If contact occurs,
    rinse thoroughly with water.

  • STOP USE

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    Directions
    • Wet hands thoroughly and allow to dry without wiping.
    • For children under 5, use adult supervision.

  • OTHER SAFETY INFORMATION

    Other information
    • Store at a temperature below 38°C (100°F)
    • Do not use if quality seal is broken

  • INACTIVE INGREDIENT

    Inactive ingredients Water (Aqua), Eucalyptus Oil, Citrus aurantium
    dulcis (Orange) Peel Oil, Hydroxypropyl Guar, Eugenia caryophyllus
    (Clove) Bud Oil, Cinnamomum zeylanicum Leaf Oil, Pyrus malus (Apple)
    Fruit Extract, Glycerin, Cinnamomum zeylanicum Bark Oil, Eucalyptus
    globulus Leaf Oil, Rosmarinus officinalis (Rosemary) Leaf/Stem Oil,
    Citric Acid

  • QUESTIONS

    Questions? Call 1-800-411-8151

  • Primary Label

    Primary PanelPrimary Label

  • INGREDIENTS AND APPEARANCE
    ON GUARD SANITIZING GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71630-098
    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
    WATER (UNII: 059QF0KO0R)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    HYDROXYPROPYL GUAR (2500-4500 MPA.S AT 1%) (UNII: 3A1I7376TC)  
    CLOVE OIL (UNII: 578389D6D0)  
    CINNAMON LEAF OIL (UNII: S92U8SQ71V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    BORON (UNII: N9E3X5056Q)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71630-098-5050 mL in 1 BOTTLE; Type 0: Not a Combination Product08/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/15/2022
    Labeler - doTERRA International, LLC (832274935)
    Establishment
    NameAddressID/FEIBusiness Operations
    Universal Packaging Systems Inc (DBA PakLabs)177711082manufacture(71630-098)