Label: MOXIE HAND SANITIZING GEL- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 15, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Ethyl Alcohol 71% V/V

  • Purpose

    Antiseptic

  • Use

    • for hand sanitizing to decrease bacteria on the skin
    • recommended for repeated use
  • Warnings

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

  • WHEN USING

    When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

  • STOP USE

    Discontinue Use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor

  • 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

    • Pump a small amount in your palm and briskly rub hands together until dry.
    • Children under 6 years of age should be supervised when in use.
  • Other Information

    Store between 15-30C (59-89F)

    Avoid freezing and excessive heat above 40C (104F)

  • Inactive ingredients

    Water, Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E).

  • QUESTIONS

    Ditributed by: Lowe's Home Centers LLC

    Mooresville NC 28117

  • Principal Display Panel

    Moxie

    HAND SANITIZER GEL

    Kills 99.9% of most common germs

    Moisturizes with Aloe & Vitamin E

    Light & Fresh Scent

    16.9 FL OZ (500ml)

    MADE IN CHINA

    Item

    Model

    MOXIE and logo deisign are trademarks or registered trademarks of LF, LLC. All rights reserved.

    Lowes Sanitizer Gel

  • INGREDIENTS AND APPEARANCE
    MOXIE HAND SANITIZING GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77720-033
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77720-033-01500 mL in 1 PACKAGE; Type 0: Not a Combination Product05/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/15/2024
    Labeler - Skaffles Group (831115642)
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