Label: THIEVES WATERLESS HAND SANITIZER WITH PEPPERMINT OIL- alcohol liquid

  • 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 9, 2021

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

View All Sections
  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 65%

    Purpose

    Antiseptic

  • Uses

    • Helps reduce bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only

    Flammable, keep away from fire, sparks, and sources of ignition.
    Do not store above 104ºF/40ºC

    When using this product

    Keep out of eyes

    • In case of contact with eyes, flush thoroughly with water 
    • Avoid contact with broken skin

    Stop use and ask a doctor if

    irritation and redness develop and persist for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • Dispense directly on hands and rub in thoroughly 
    • For children under 6, use adult supervision 
    • Not recommended for infants
  • Inactive ingredients

    Water, Aloe barbadensis leaf powder, Glycerin, Hydroxypropylcellulose, Mentha piperita† (Peppermint) oil, Eugenia caryophyllus† (Clove) bud oil, Citrus limon† (Lemon) peel oil, Eucalyptus radiata† leaf oil, Rosmarinus officinalis† (Rosemary) leaf oil, Cinnamomum zeylanicum† (Cinnamon) bark oil
    †100% pure, therapeutic-grade essential oil

  • Thieves Waterless Hand Sanitizer with Peppermint Oil, 30mL (70631-036-30)

    Label

  • Thieves Waterless Hand Sanitizer with Peppermint Oil, 225mL (70631-036-25)

    Label2

  • INGREDIENTS AND APPEARANCE
    THIEVES WATERLESS HAND SANITIZER WITH PEPPERMINT OIL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70631-036
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL650 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    CLOVE (UNII: K48IKT5321)  
    LEMON (UNII: 24RS0A988O)  
    EUCALYPTUS RADIATA LEAF OIL (UNII: SB9A7612BD)  
    ROSEMARY (UNII: IJ67X351P9)  
    CINNAMON (UNII: 5S29HWU6QB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70631-036-3030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/24/2018
    2NDC:70631-036-25225 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/24/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/24/2018
    Labeler - Young Living Essential Oils, LC (836136630)
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!