Label: 3ECARE DUAL FORMULATOOTHPASTEFOR SENSITIVETEETH- potassium nitrate sodium monofluorophosphate paste, dentifrice

  • NDC Code(s): 87514-004-02
  • Packager: Hangzhou Namei Zhikang Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 2, 2026

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

  • PURPOSE


    ·aids in the prevention of dental cavities.
    ·helps reduce and builds increasing protection against painful
    sensitivity of the teeth to cold, heat, acids, sweets, or contact.

  • WARNINGS


    It shall be used with electric dual toothpaste dispenser.

    Stop use and ask a dentist if

    ·the problem persists or worsens. Sensitive teeth may indicate a
    serious problem that may need prompt care by a dentist.
    ·pain/sensitivity still persists after 4 weeks of use.

  • KEEP OUT OF REACH OF CHILDREN


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

  • INSTRUCTIONS FOR USE


    ①Please use it with electric dual toothpaste dispenser;②Mount
    dual-formula toothpaste on the electric dispenser according to the
    instructions for use;③For the first use, unscrew the cap and remove
    the sealing sticker on the opening of toothpaste tube;④When the
    electric dispenser is turned on, press the Squeeze button to squeeze
    the toothpaste,release the button to stop squeezing, then apply the
    toothpaste to the toothbrush.

  • DOSAGE & ADMINISTRATION


    ·do not swallow .supervise children as necessary
    until capable of using without supervision
    ·adults and children 12 years of age and older:
    ·apply at least a 1-inch strip of the product onto a soft bristle
    toothbrush.
    ·brush teeth thoroughly for at least 2 minute twice a day (morning
    and evening) or as recommended by a dentist or doctor. Make
    sure to brush all sensitive areas of the teeth. Spit out after
    brushing.
    ·children under 12 years of age: Consult a dentist or doctor

  • INACTIVE INGREDIENT


    A Tube: glycerin, hydrated silica, propylene glycol, calcium sodium
    phosphosilicate, cocamidopropyl betaine, polyoxyl 15
    hydroxystearate, PEG-20, aroma, hydroxyapatite, PVP, titanium
    dioxide, zinc citrate, sucralose, carboxymethyl chitosan, triacetin.
    B Tube: glycerin, water, hydrated silica,potassium nitrate, PEG-8,
    betaine, cocamidopropyl betaine, aroma, sodium lauryl sulfate,
    xanthan gum, sodium hydroxide, zinc citrate, strontium chloride
    hexahydrate, carbomer, arginine, sucralose, sodium carbonate,
    sodium bicarbonate, carboxymethyl chitosan, calcium aluminum
    borosilicate, tin oxide, titanium dioxide, blue 2.

  • INDICATIONS & USAGE

    Uses

    aids in the prevention of dental cavities.
    helps reduce and builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact.

  • PRINCIPAL DISPLAY PANEL

    a

  • INGREDIENTS AND APPEARANCE
    3ECARE DUAL FORMULATOOTHPASTEFOR SENSITIVETEETH 
    potassium nitrate sodium monofluorophosphate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87514-004
    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 MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 1 g  in 100 g
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87514-004-021 g in 1 BOX; Type 0: Not a Combination Product03/20/2026
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02103/20/2026
    Labeler - Hangzhou Namei Zhikang Technology Co., Ltd. (413965495)
    Registrant - Hangzhou Namei Zhikang Technology Co., Ltd. (413965495)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hangzhou Namei Zhikang Technology Co., Ltd.413965495api manufacture(87514-004)