Label: CLINPRO 5000- sodium fluoride paste, dentifrice

  • NDC Code(s): 48878-3120-1, 48878-3120-2
  • Packager: 3M ESPE Dental Products
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated November 30, 2021

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

  • Principal Display Panel – CA Box Label

    3M ESPE

    ClinproMC 5000

    Menthe-vanille

    Dentifrice anticarie au

    fluorure de sodium à 1,1 %

    Formule de

    diphosphate

    tricalcique

    novatrice

    Offerte uniquement par 3M ESPE

    Contenu : 1 tube POIDS NET : 113 g (4 oz)

    NPN 80012416

    Principal Display Panel – CA Box Label
  • Principal Display Panel – CA Tube Label

    3M ESPE

    ClinproTM MC 5000

    Vanilla Mint

    Menthe vanilla

    1.1% Sodium Fluoride Anti-Cavity Toothpaste

    Dentifrice anticarie au flourure de sodium à 1,1 %

    NET WT 113 g (4 oz) / POIDS NET : 133 g (4 oz)

    NPN 80012416

    Innovative

    Tri-Calcium

    Phosphate

    Exclusively from 3M ESPE

    Formule de

    diphosphate

    tricalcique

    innovante

    Offerte uniquement par 3M ESPE

    Principal Display Panel – CA Tube Label
  • Principal Display Panel – AU/NZ Box Label

    PHARMACIST ONLY MEDICINE

    KEEP OUT OF REACH OF CHILDREN

    3M

    Clinpro™ 5000

    Sodium Fluoride 1.1% w/w

    Vanilla Mint

    Anti-Cavity Toothpaste

    For use after professional recommendation.

    Contains: 1 Tube NET WT 113g

    AUST R 219455

    Principal Display Panel – AU/NZ Box Label
  • Principal Display Panel – AU/NZ Tube Label

    PHARMACIST ONLY MEDICINE

    KEEP OUT OF REACH OF CHILDREN

    3M

    Clinpro™ 5000

    Sodium Fluoride 1.1% w/w

    Vanilla Mint

    Anti-Cavity Toothpaste

    For use after professional recommendation.

    NET WT 113g

    AUST R 219455

    Principal Display Panel – AU/NZ Tube Label
  • INGREDIENTS AND APPEARANCE
    CLINPRO 5000 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:48878-3120
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    sodium fluoride (UNII: 8ZYQ1474W7) (fluoride ion - UNII:Q80VPU408O) fluoride ion5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Sorbitol (UNII: 506T60A25R)  
    Silicon Dioxide (UNII: ETJ7Z6XBU4)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)  
    Sodium Lauryl Sulfate (UNII: 368GB5141J)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Carboxymethylcellulose Sodium (UNII: K679OBS311)  
    Saccharin Sodium (UNII: SB8ZUX40TY)  
    Tricalcium Phosphate (UNII: K4C08XP666)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINT (MINT) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48878-3120-11 in 1 BOX08/10/2009
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:48878-3120-21 in 1 BOX09/01/201711/30/2021
    2113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only08/10/2009
    Labeler - 3M ESPE Dental Products (801390852)