Label: SIMPLIFY ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic

  • Use

    to decrease bacteria on the skin

  • Warnings

    For external use only-hands

    Keep out of the reach of children. If swallowed, get

    medical help or contact a Poison Control Center right away.

    When using this product

    • Keep out of eyes. In case of contact with eyes, flush

    thoroughly with water.

    • avoid contact with broken skin

    Stop use and ask a doctor if

    • irritation or redness develops
    • condition persists for more than 72 hours
  • SPL UNCLASSIFIED SECTION

    Drug Facts (continued)

  • Directions

    • wipe hands thoroughly with product and

    allow to dry

    • for children under 6, use only under adult

    supervision

    • not recommended for infants
  • Inactive Ingredients

    water (aqua), glycerin, sodium benzoate, potassium sorbate,
    aloe barabadensis leaf juice, fragrance (parfum),
    caprylyl/capryl glucoside, polyglyceryl-4 laurate/sebacate,
    polyglyceryl-6 caprylate/caprate, citric acid, polysorbate 20

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY: RITE AID,
    2.00 NEWBERRY COMMONS, ETTERS. PA 17319
    www.riteaid.com

    *Testing based on a subset of FDA proposal published June 17, 1994.

  • 20 Wipes 5.5 x 7 in (14 x 17.8 cm)

    Simplify ®

    Antibacterial

    Hand Wipes

    Gentle Cleansing

    • With aloe
    • Scented
    • Kills 99.9% of

    Most Common Germs*

    • Dermatologist Tested

    20 Hand Wipes

    OPEN

    Do Not Flush

    5.5 x 7 in (14 x 17.8 cm)

    Front panelGraphicsDrug factsDrug Facts continued

  • INGREDIENTS AND APPEARANCE
    SIMPLIFY ANTIBACTERIAL HAND WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0283
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    POLYGLYCERYL-6 CAPRYLATE (UNII: DGV8R54VG7)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POLYGLYCERYL-4 LAURATE (UNII: 82V7NG3DYT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0283-120 in 1 POUCH; Type 0: Not a Combination Product09/11/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/11/2023
    Labeler - Rite Aid Corporation (014578892)
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