Label: WALGREENS ADVANCED HAND SANITIZER WITH VITAMIN E- 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 August 11, 2020

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  • Drug Facts

  • Active ingredient

    Alcohol 69% v/v

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    For external use only

    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 a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help 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
  • Other information

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

    Water, Glycerin, Propylene Glycol, Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Denatonium Benzoate.

  • Company Information

    DISTRIBUTED BY: WALGREEN CO.,

    200 WILMOT RD., DEERFIELD, IL 60015

  • Product Packaging - 236 mL

    Walgreens

    ADVANCED

    Hand

    Sanitizer

    + VITAMIN E

    • Leaves hands soft
    • Contains moisturizers
    • Kills 99.9% of common germs

    8 FL OZ (236 mL)

    sanitizer vite

  • INGREDIENTS AND APPEARANCE
    WALGREENS ADVANCED HAND SANITIZER WITH VITAMIN E 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL69 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9004-01236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/11/2020
    2NDC:0363-9004-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/11/2020
    3NDC:0363-9004-03887 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/11/2020
    Labeler - Walgreen Company (008965063)
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