Label: POP FEELING PEACHY- sodium fluoride paste, dentifrice

  • NDC Code(s): 43136-512-20
  • Packager: TAI GUK PHARM. CO., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

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  • Drug Facts

    Drug Facts

  • Active Ingredient

    SODIUM FLUORIDE 0.243% (0.14% w/v fluoride ion)

  • Purpose

    Anticavity toopaste

  • Use

    helps protect against cavities

  • Warnings

    Warnings

    Keep out of reach of children.

    Keep out of reach of children under 6 years of age. Do not swallow. If you accidentally swallow more than used for brushing, seek professional assistance or contact a poison control center right away. If an allergic reaction develops, discontinue use immediately.

  • Directions

    • adults and children 2 years of age and and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist.
    • ​do not swallow.
    • ​to minimize swallowing use a pea-sized amount in children under 6.
    • ​supervise children's brushing until good habits are established.
    • ​ children under 2 years: ask a dentist.
  • Inactive Ingredients

    WATER, SORBITOL, HYDRATED SILICA, SODIUM LAURYL SULFATE, GLYCERIN, CELLULOSE GUM, FLAVOR, TETRASODIUM PYROPHOSPHATE, ZINC STEARATE, XANTHAN GUM, SODIUM SACCHARIN, TITANIUM DIOXIDE, SORBITAN OLEATE, HYDROXYAPATITE, NIACINAMIDE, TOCOPHERYL ACETATE, XYLITOL

  • Questions?

    1-866-993-4709

  • Principal Display Panel - 120 g Tube Carton

    POP

    Playful. Original. Personal

    REPAIRS ENAMEL
    PREVENTS CAVITIES
    FRESHENS BREATH


    FEELING PEACHY

    Fluoride Toothpaste
    with Hydroxyapatite &
    Vitamins E and B3

    NET WT. 4.2 OZ. (120 G)

    DIST. LG H&H CO., LTD.
    58, SAEMUNAN-RO, JONGNO-GU, SEOUL, KOREA
    www.oralcarebypop.com

    MADE IN KOREA

    POP_Feeling_Peachy_120g_OC

    POP_Feeling_Peachy_120g_IC

  • INGREDIENTS AND APPEARANCE
    POP FEELING PEACHY 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43136-512
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.4 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    WATER (UNII: 059QF0KO0R)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    XYLITOL (UNII: VCQ006KQ1E)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorPEACHImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43136-512-201 in 1 CARTON11/17/2023
    1120 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02111/17/2023
    Labeler - TAI GUK PHARM. CO., LTD (689060246)
    Registrant - LG H&H CO., LTD. (688276187)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tai Guk Pharma. Co., Ltd.689060246manufacture(43136-512)
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