Label: MEDPRIDE ANTIBACTERIAL HAND WASH- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL

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 January 13, 2022

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  • Drug Facts

    Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.13%(w/w)

  • Purpose

    Antibacterial

  • Uses

    • For washing hand to decrease bacteria on the skin
  • Warnings

    For external use only

  • When using this product

    • Avoid contact with eyes. In case of eye contact, flush with water.
  • Stop use and ask a doctor if

    irritation and redness develops

  • Keep out of reach of children

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

  • Directions

    pump onto wet hands, vigorously work into lather rinse thoroughly

  • other information

    Store in a cool dry place below 104 F

  • Inactive Ingredients

    Benzophenone-4, Benzyl Alcohol, CI 42090, Citric Acid, Cocamide DEA, Cocamidopropyl Betaine, Fragrance, Glycerin, Lauryl Glucoside, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Chloride, Sodium Laureth Sulfate, Water

  • PRINCIPAL DISPLAY PANEL

    Drug Fact Panel

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE ANTIBACTERIAL HAND WASH 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-8092
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52410-8092-1400 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/04/2020
    Labeler - Shield Line LLC (078518916)
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