Label: CB ALCOHOL WIPES- benzalkonium chloride swab swab

  • 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 March 24, 2020

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  • Active Ingredient

    Benzalkonium chloride 0.1%

  • Purpose

    Antibacterial

  • Use

    decreases bacteria on skin

  • Directions

    For adults and children of 2 years and over.

    Children under 2 years ask a doctor before use.

    Allow to dry without wiping.

  • Warnings

    For external use only.

    Do not use

    over large areas of the body

    if you are allergic to any of the ingredients

    when using this product,avoid contact with eyes and face.

    If contact occurs,flush thoroughly with water.

    Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact aPoisonControlCenter right away.

  • Inactive Ingredients

    water,sodium lauryl sulfate,fragrance,2-bromo-2-nitropropane-1,3-diol,aloe barbadensis leaf extract,disodium EDTA,trithanolamine ,glycerin,tocopheryl acetate

  • PRINCIPAL DISPLAY PANEL

    CB Alcohol Wipes

  • INGREDIENTS AND APPEARANCE
    CB ALCOHOL WIPES 
    benzalkonium chloride swab swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73529-352
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CUPRIC BIS(TRIETHANOLAMINE) (UNII: YBM44X0B6H)  
    2-BROMO-2-NITROETHANOL (UNII: FA22WV2B2Z)  
    WATER (UNII: 059QF0KO0R)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73529-352-010.1 g in 1 POUCH; Type 0: Not a Combination Product03/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/16/2020
    Labeler - Nutritech Pharmaceuticals, Inc (117342868)
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