Label: 719 WALNUT AVE HAND FRESH ALOE- benzalkonium chloride 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 May 21, 2017

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

  • Drug Factsactive ingredients

    Benzalkonium Chloride

  • Purpose

    Antiseptic

  • Use

    hand sanitizer to help reduce bacteria on skin

  • Warnings

    For external use only.

    Flammable Keep away from heat and flame. Do not store 104°F/40°C

  • Stop use and ask a doctor if

    irritation ot redness develops.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222).

  • Directions

    Wet hands thoroughly with the product and rub skin until dry. Children under 6 years of age should be supervised by an adult when using.

  • Inactive Ingredients

    Cetrimonium Chloride, Citric Acid, Dimethicone, Disodium Cocoamphodiacetate, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Tetrasodium EDTA Water (Aqua).

  • 719 WALNUT AVE® FOAMING HAND SANITIZER fresh aloe product label

    719 WALNUT AVE®

    FOAMING HAND SANITIZER
    fresh aloe

    2 fl OZ (60 mL)

    NDC 29500-0555-1

    Distributed by:
    Wal-Mart Stores, Inc.
    Bentonville, AR 72716

    Made in China

    PC-WM WalnutAve FoamHand San - 555

  • INGREDIENTS AND APPEARANCE
    719 WALNUT AVE HAND  FRESH ALOE
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-0555
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE78 mg  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29500-0555-160 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/19/2017
    Labeler - Personal Care Products (966155082)
    Registrant - Personal Care Products (966155082)