Label: FRANKLIN CLEANING TECHNOLOGY ANTIBACTERIAL HAND- chloroxylenol liquid

  • NDC Code(s): 60933-056-00
  • Packager: Fuller Industries, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 28, 2023

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  • Drug Facts

  • Active ingredient

    Chloroxylenol 0.3%

    Purpose

    Antiseptic

  • Uses

    • For hand washing to decrease the bacteria on skin.
    • Recommended for repeated use
  • Warnings

    For external use only

    Do not use

    in the eyes. In case of contact, flush eyes with water.

    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

    • Pump a small amount of foam into palm of hand
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together to produce a thick lather
    • Rinse and repeat
  • Inactive ingredients

    DEIONIZED WATER, SODIUM LAURYL ETHER SULFATE, SODIUM CHLORIDE, COCAMIDE MIPA, SODIUM SULFATE, OCEAN BREEZE FRAGRANCE 16295, MAGNESIUM NITRATE, CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FD & C YELLOW #6, D&C RED NO. 33

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    FRANKLIN CLEANING TECHNOLOGY ANTIBACTERIAL HAND 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60933-056
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60933-056-003790 mL in 1 BOTTLE; Type 0: Not a Combination Product04/28/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/28/2023
    Labeler - Fuller Industries, Inc (078704329)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fuller Industries, Inc078704329manufacture(60933-056)
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