Label: CLEAR S SUDS- benzethonium chloride solution

  • 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 6, 2020

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  • Active Ingredient

    Benzethonium Chloride 0.13%

  • Purpose

    Antiseptic

  • Uses

    • For handwashing to decrease bacteria on the skin.
  • Warnings

    For external use only.

    Do not use in the eyes.

    Discontinue use if irritation and redness develops.

    If condition persists for more than 72 hours consult a doctor.

    Keep out of reach of children.

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

  • Directions

    • Apply to hands and wet as needed.
    • Lather vigorously for at least 15 seconds.
    • Wash skin, rinse thoroughly and dry.
  • Other information

    Protect from freezing.

    Avoid excessive heat.

    Store at 40-95 F (4-35 C).

  • Inactive ingredients

    Purified Water, Cocamidopropyl Betaine, Laramine Oxide, Glycerin, Cetrimonim Chloride, Fragrance, DMDM Hydantoin, Iodopropynyl Carbamate, Yellow 6, Red 4, (may contain Citric Acid, Sodium Hydroxide)

  • Questions?

    Call 1-855-797-2257

  • PRINCIPAL DISPLAY PANEL

    CLEAR

    The Choice Is Clear

    SOAP SUDS

    Antibacterial Soap

    purpose:

    cleans + moisturizes

    scent:

    floral

    8.5 Fl.Oz. 125mL

    A Brand By PHARMAPACKS

    container label

  • INGREDIENTS AND APPEARANCE
    CLEAR S SUDS 
    benzethonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73599-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73599-003-09250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/06/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/06/2020
    Labeler - PHARMAPACKS, LLC (079254738)
    Establishment
    NameAddressID/FEIBusiness Operations
    Central Solutions, Inc.007118524manufacture(73599-003)
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