Label: EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E- ethyl alcohol gel

  • 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 April 7, 2020

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  • Active ingredient

    ETHYL ALCOHOL 65%

  • Purpose

    Antiseptic

  • Uses

    • Decreases bacteria on the skin that could cause disease
    • recommended for repeated use

  • WARNINGS

    For external use only: hands
    Flammable, keep away from fire or flame.
    When using this product
    • keep out of eyes. In case of contact with eyes flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest

    Stop use and ask doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours
  • Keep out of reach of children.

    If swallowed, get medical hep or contact a Poison Control Center right away.

  • Directions

    • wet hands thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants

  • Other information

    • not store above 105°F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredient

    water, glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, triethanolamine, fragrance, tocopheryl acetate, panthenol

  • Questions?

    1-888-287-1915

  • PRINCIPAL DISPLAY PANEL

    EQT_12oz_Orig_GelHandSanitizer_V2

  • INGREDIENTS AND APPEARANCE
    EQUATE MOISTURIZING HAND SANITIZER WITH VITAMIN E 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-557
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 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)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-557-0389 mL in 1 BOTTLE; Type 0: Not a Combination Product04/07/2020
    2NDC:49035-557-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product04/07/2020
    3NDC:49035-557-341000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/2020
    Labeler - Wal-Mart Stores, Inc. (051957769)
    Registrant - Wal-Mart Stores, Inc. (051957769)
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