UP AND UP ANTICAVITY TOOTHPASTE WHITENING PLUS MOUTHWASH (SODIUM FLUORIDE) PASTE, DENTIFRICE [TARGET CORPORATION]

UP AND UP ANTICAVITY TOOTHPASTE WHITENING PLUS MOUTHWASH (SODIUM FLUORIDE) PASTE, DENTIFRICE [TARGET CORPORATION]
PDF | XML

NDC 11673-090-01, 11673-090-02
Set ID 24d1223e-2cc4-4f84-9f0d-6d79bf6da4c4
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class
Product Number
Application Number PART355
  • Active Ingredient

    Sodium fluoride 0.243% (0.15% w/v fluoride ion)... Anticatity toothpaste
  • USE

    Helps protect against cavities
  • WARNINGS

    As with all fluoride toothpastes, keep out of reach of children under 6 years of age. If you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.

  • Directions

    Adults and children 2 years and older     Brush teeth thoroughly, PREFERABLY AFTER EACH MEAL,or at least twice a day,                                                                          or  as directed by your dentist. DO NOT SWALLOW
    Children under 6 years of age                   To minimize swallowing, use a pea-sized amount and supervise brushing until good                                                                          habits are established.
    Children under 2 years                               ASK A dentist or physician

  • Inactive Ingredients:

    Sorbitol, Water, HYDRATED SILICA, PEG-6, Sodium Lauryl Sulphate, Alcohol (1.14%), Flavor, Xanthan Gum, Carbomer, Sodium Benzoate, Titanium Dioxide, Tetrasodium Pyrophosphate, Sodium Saccharin, Triclosan, Blue 1, Yellow 4.
  • Principal Display Panel

    image of container
  • PURPOSE

    Anticatity toothpaste
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INGREDIENTS AND APPEARANCE
    UP AND UP ANTICAVITY TOOTHPASTE WHITENING PLUS MOUTHWASH 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-090
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE 2.43 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    ALCOHOL (UNII: 3K9958V90M) 1.14 mg  in 1 g
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOMER 934 (UNII: Z135WT9208)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorMINT (Minty Fresh) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-090-021 in 1 CARTON
    1NDC:11673-090-01181.4 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35505/31/2011
    Labeler - Target Corporation (006961700)

Related Drugs