Label: CLEARLY BETTER- foaming hand sanitizer liquid

  • NDC Code(s): 67502-391-27
  • Packager: Intercon Chemical Company
  • 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 February 15, 2023

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  • claims

    Clearly Better

    by INTRTCON

    ALCOHOL FREE FOAMING HAND SANITIZER

  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic

  • Use

    • to decrease bacteria on the skin that could cause disease
  • Warnings

    For exterenal use only-hands

  • When using this product

    • avoid contact with eyes.  if contact occurs, rinse eyes thoroughly with water.
    • avoid contact with broken skin
  • Stop use and ask a doctor if

    • irritation or redness develops
    • condition persists for mre than 72 hours
  • Keep out of reach of children.

    If swallowed, get medical help or contract a Poison Control Cener right away

  • Directions

    • wet hands thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants
  • Inactive ingredients

    cetrimonium chloride, diglycerol, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, methylchloroisothiazolinone, methylisothiazolinone, tetrasodium EDTA, water

  • Adverse Reactions Section

    DISTRIBUTED BY: INTERCON CHEMICAL CO.

    1100 CENTRAL INDUSTRIAL DR.

    ST. LOUIS, MO 63110

  • Principal display panel

    ClearlyBetter

    BY INTERCON

    ALCOHOL FREE

    FOAMING

    HAND SANITIZER

    1150 mL (39 FL OZ)

    image description

  • INGREDIENTS AND APPEARANCE
    CLEARLY BETTER 
    foaming hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67502-391
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    DIGLYCERIN (UNII: 3YC120743U)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    glycerin (UNII: PDC6A3C0OX)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M7P1JZ2V2)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67502-391-271150 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product08/28/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/28/2017
    Labeler - Intercon Chemical Company (103204970)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(67502-391)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(67502-391)
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