Label: BOP WHITENINGTOOTHPASTE- bop whitening toothpaste gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 22, 2022

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

  • ACTIVE INGREDIENT

    XYLITOL

    GLYCYRRHIZINATE DIPOTASSIUM

  • INACTIVE INGREDIENT

    Sorbitol Hydrated silica, Water, Sodium Lauroyl Sarcosinate,Sodium Phytate, Polyethylene Glycol 1600,Hydroxyapatite,Menthol,

    sucralose,Hyaluronate Sodium,Chondrus Crispus Carrageenan,Pistacia Lentiscus Resin,Menthone 1,2-Glycerol

    Ketal,Hydroxyacetophenone, Caprylyl Glycol,1,2-Hexanediol,Sodium Phpsphate,Titanium Dioxide.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children under 6 yrs. of age.

  • PURPOSE

    Anticavity
    Anti-inflammatory

  • Use

    Help protect against cavities and diminish inflammation.

  • Directions

    Adults and children 2 yrs.& older: brush teeth thoroughly aftermeals 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 brushing until good habits are established.
    Children under 2 yrs.: ask a dentist.

  • STORAGE AND HANDLING

    Store in a dry and cool place.

  • WARNINGS

    Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    BOP WHITENINGTOOTHPASTE 
    bop whitening toothpaste gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82574-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) (GLYCYRRHIZIN - UNII:6FO62043WK) GLYCYRRHIZINATE DIPOTASSIUM0.3 g  in 100 g
    XYLITOL (UNII: VCQ006KQ1E) (XYLITOL - UNII:VCQ006KQ1E) XYLITOL3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)  
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
    5-METHYL-1,3,5-TRIPHENYL-2-PYRAZOLINE (UNII: 96K6O83026)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    PISTACIA LENTISCUS RESIN (UNII: 7446H202QW)  
    MENTHONE 1,2-GLYCEROL KETAL, (+/-)- (UNII: 7QQ1EE6RCP)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    SORBITOL (UNII: 506T60A25R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    MENTHOL (UNII: L7T10EIP3A)  
    CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82574-001-01100 g in 1 PACKAGE, COMBINATION; Type 0: Not a Combination Product02/22/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/22/2022
    Labeler - Shanghai Gemang Trading Co., Ltd. (706982437)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shanghai Gemang Trading Co., Ltd.706982437manufacture(82574-001)