Label: EXODEN POWDER- cetylpyridinium chloride, domiphen bromide powder

  • NDC Code(s): 70602-003-01, 70602-003-02, 70602-003-03, 70602-003-04, view more
    70602-003-05, 70602-003-06
  • Packager: LIFEON Corp.
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated March 9, 2021

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  • ACTIVE INGREDIENT

    Cetylpyridinium Chloride(CPC) 0.43%
    Domiphen Bromide 0.120

  • PURPOSE

    Oral Health Care

  • INDICATIONS & USAGE

    Provide better health to teeth and gums

  • DOSAGE & ADMINISTRATION


    Wet your toothbrush, shake off surplus water and press into powder. Brush teeth thoroughly and rinse

  • WARNINGS

    Ask a dentist before use if you have
    • bleeding or redness lasting more than 2 weeks
    • pain, swelling, pus, loose teeth, or more spacing between teeth
    These may be signs of periodontitis, a serious form of gum disease

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away

  • INACTIVE INGREDIENT

    Bentonite, Sodium Chloride(Bamboo Salts), L-Menthol

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    EXODEN POWDER 
    cetylpyridinium chloride, domiphen bromide powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70602-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOMIPHEN BROMIDE (UNII: R4CY19YS7C) (DOMIPHEN - UNII:4AZL56CU0F) DOMIPHEN BROMIDE0.12   in 100 g
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.043 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENTONITE (UNII: A3N5ZCN45C)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70602-003-021 in 1 CARTON03/09/2021
    1NDC:70602-003-0110 g in 1 POUCH; Type 0: Not a Combination Product
    2NDC:70602-003-041 in 1 CARTON03/09/2021
    2NDC:70602-003-0330 g in 1 CONTAINER; Type 0: Not a Combination Product
    3NDC:70602-003-061 in 1 CARTON03/09/2021
    3NDC:70602-003-0570 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/09/2021
    Labeler - LIFEON Corp. (688528872)
    Registrant - LIFEON Corp. (688528872)
    Establishment
    NameAddressID/FEIBusiness Operations
    Korea Shidenta688171734manufacture(70602-003)
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