Label: AMERFRESH TOOTH- sodium monofluorophosphate powder

  • NDC Code(s): 70766-005-01, 70766-005-02
  • Packager: Yangzhou SION Commodity Co.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 8, 2023

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  • Active ingredients

    SODIUM MONOFLUOROPHOSPHATE 0.76%(0.1 w/v Fluoride ion)

    Purpose

    anticavity 

  • Uses

    aids in the prevention of dental cavities.

  • Warnings

    Keep out of the reach of children under 6 years of age.if more than used for brushing is accidently swallowed,get medical help or contact a Poison Control Center immediately.

    Keep out of reach of children.

  • Directions

    For Use:

    • Wet toothbrush and dip into powder until brush is fully covered
    • do not swallow .
    • supervise children as necessary until capable of useing without supervision
    • instruct children under 12 years of age in good brushing and rinsing habits(to minimize swallowing).
    • Adults and children 6 years of age and older:Brush teeth thoroughly,preferably after each meal or at least twice a day,or as directed by a dentist or a physician.
    • Children under 6 years of age:do not use unless directed by a doctor or dentist.
  • INACTIVE INGREDIENT

    calcium carbonate, silica,sodium lauryl sulfate, flavor, sodium sacharine, methylisothiazolinone

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    AMERFRESH TOOTH 
    sodium monofluorophosphate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70766-005
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U)  
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70766-005-0140 in 1 CARTON04/20/2018
    1454 g in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:70766-005-024 in 1 CARTON04/20/2018
    250 in 1 BOX
    257 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02104/20/2018
    Labeler - Yangzhou SION Commodity Co.,Ltd (546806042)
    Registrant - Yangzhou SION Commodity Co.,Ltd (546806042)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yangzhou SION Commodity Co., Ltd546806042manufacture(70766-005)