Label: HAND SANITIZER MOJITO MINT- organic ethyl alcohol gel

  • NDC Code(s): 42681-6895-1
  • Packager: Whole Foods Market, Inc.
  • 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 March 22, 2021

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  • ACTIVE INGREDIENT

    Active Ingredient

    Ethyl Alcohol 62% v/v

  • PURPOSE

    Purpose

    Antiseptic

  • WARNINGS

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

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor if skin irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

  • INDICATIONS & USAGE

    Uses to help reduce bacteria on the skin

  • DOSAGE & ADMINISTRATION

    Directions apply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.

  • STORAGE AND HANDLING

    Other information do not store above 104°F (40°C).

  • QUESTIONS

    Questions, Comments?

    customer.questions@wholefoods.com

    1-844-963-8255

  • INACTIVE INGREDIENT

    Inactive ingredients water, isopropyl alcohol, hydroxyethylcellulose, salvia hispanica (chia) seed oil, glycerin, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract, fragrance (natural), triethyl citrate.

  • PRINCIPAL DISPLAY PANEL

    Mojito Mint Gel 1fl oz

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  MOJITO MINT
    organic ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42681-6895
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
    CHIA SEED OIL (UNII: MC2LH51BO7)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ROSEMARY (UNII: IJ67X351P9)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42681-6895-130 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/202012/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/202012/31/2024
    Labeler - Whole Foods Market, Inc. (196175616)
    Registrant - V Manufacturing & Logistics, Inc. (825176857)
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