Label: ETT HOJAKDO SENSITIVITY AND CAVITY CARE- potassium nitrate, sodium fluoride paste, dentifrice

  • NDC Code(s): 83672-002-01, 83672-002-02
  • Packager: LIFE STEALER Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

If you are a consumer or patient please visit this version.

  • active ingredient

    Potassium Nitrate 5%

    Sodium Fluoride 0.315%

  • 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

  • Purpose

    Antihypersensitivity, Anticavity

  • Uses

    - Builds increasing protection against painful sensitivity of the
    teeth to cold, heat, acids, sweets or contact
    - Helps protect against cavities

  • 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

  • Directions

    Supervise children as necessary until capable of using without supervision

    Adults and children 12 years of age and older: Brush teeth thoroughly, preferably after each meal or at least 3 minutes twice a day (morning and evening), or as directed by a dentist or a physician

    Children under 12 years of age: Consult a dentist or doctor

  • Inactive Ingredients

    Glycerin, Water, Hydrated Silica, Hydroxyapatite, Sorbitol, Cellulose Gum, Sodium Fluoride, Xylitol, Sodium Saccharin, Xanthan Gum, Foeniculum Vulgare Oil, Menthol, Sodium Cocoyl Glutamate, Chamomilla Recutita Flower Extract, Calendula Officinalis Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Stevia Rebaudiana Extract

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    ETT HOJAKDO SENSITIVITY AND CAVITY CARE 
    potassium nitrate, sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83672-002
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE5 g  in 100 g
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.315 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    STEVIA REBAUDIANA WHOLE (UNII: 6U422Y08O2)  
    SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    ROSEMARY (UNII: IJ67X351P9)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    FOENICULUM VULGARE WHOLE (UNII: J1UK54JBGH)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83672-002-021 in 1 CARTON12/11/2024
    1NDC:83672-002-01100 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02112/11/2024
    Labeler - LIFE STEALER Co., Ltd. (695909253)
    Registrant - LIFE STEALER Co., Ltd. (695909253)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sejung Medical Co., Ltd.963252282manufacture(83672-002)