Label: ADOPTAPLATOON- sodium monofluorophosphate paste

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    71167-001-01, 71167-001-02, 71167-001-03, 71167-001-04, view more
    71167-001-05, 71167-001-06, 71167-001-07, 71167-001-08, 71167-001-09, 71167-001-10, 71167-001-11, 71167-001-12
  • Packager: HUAIAN ZONGHENG BIO-TECH CO., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 13, 2017

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

  • Active Ingredient

    sodium monofluorphosphate  0.76%

  • Purpose

    Anticavitytoothpaste

  • Use

    helps protect against cavities

  • Warning

    Keep out of 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 right away.

  • Directions

    Adults and children 6 years of age and older:brush teeth thoroughly, after meals or at least twice a day or use as directed by a dentist.

    do not swallow

    to minimize swallowing use a pea-sized amount in children under 6

    supervise children's burshing ntil good habits are established

    children under 2 years ask a dentist

  • Inactive Ingredients

    Calcium Carbonate,Aqua,Glycerin,Sorbitol,Silica,Aroma,Sodium Lauryl Sulphate,Carboxymethyl Hydroxyethyl cellulose,Chondrus Crispus,CI77891(Titanium Dioxide),Sodium saccharin,rose canina fruit oil

  • Keep out of reach of children under 6 years of age

    Keep out of reach of children under 6 years of age

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    ADOPTAPLATOON 
    sodium monofluorophosphate paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71167-001
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.76 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CHONDRUS CRISPUS (UNII: OQS23HUA1X)  
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM SILICATE (UNII: IJF18F77L3)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)  
    POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U)  
    ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71167-001-0110 g in 1 TUBE; Type 0: Not a Combination Product01/13/2017
    2NDC:71167-001-0225 g in 1 TUBE; Type 0: Not a Combination Product01/13/2017
    3NDC:71167-001-0330 g in 1 TUBE; Type 0: Not a Combination Product01/13/2017
    4NDC:71167-001-0424 in 1 BOX07/10/2016
    4150 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:71167-001-0548 in 1 BOX07/10/2016
    5150 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:71167-001-0648 in 1 BOX07/10/2016
    6150 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:71167-001-07288 in 1 BOX07/10/2016
    750 g in 1 TUBE; Type 0: Not a Combination Product
    8NDC:71167-001-08144 in 1 BOX07/10/2016
    860 g in 1 TUBE; Type 0: Not a Combination Product
    9NDC:71167-001-09144 in 1 BOX07/10/2016
    970 g in 1 TUBE; Type 0: Not a Combination Product
    10NDC:71167-001-1072 in 1 BOX07/10/2016
    1085 g in 1 TUBE; Type 0: Not a Combination Product
    11NDC:71167-001-11144 in 1 BOX07/10/2016
    1185 g in 1 TUBE; Type 0: Not a Combination Product
    12NDC:71167-001-12144 in 1 BOX07/10/2016
    12100 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35507/10/2016
    Labeler - HUAIAN ZONGHENG BIO-TECH CO., LTD (527152733)
    Establishment
    NameAddressID/FEIBusiness Operations
    HUAIAN ZONGHENG BIO-TECH CO., LTD527152733manufacture(71167-001)