Label: BUBBLE FRESH TOOTHPASTE, WITH FLUORIDE paste

  • NDC Code(s): 67777-191-01, 67777-191-02, 67777-191-03, 67777-191-04, view more
    67777-191-05, 67777-191-06, 67777-191-07, 67777-191-08, 67777-191-09, 67777-191-10
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2024

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  • Active Ingredient

    Sodium Fluoride 0.22%

  • Purpose

    Anticavity

  • Use(s)

    Helps protect against cavities

  • Warnings

    Do Not Swallow

    Keep our to reach of children under 6 years of age

    If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

  • Directions

    • Adults and children 2 years of age and older: Brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or physician.

    • Children under 6 years: To minimize swallowing, use a pea size amount and supervise child's brushing and rinsing until good habits are established.

    • Children under 2 years: Use as directed by a dentist or physician

  • Inactive Ingredients

    Carboxymethylcellulose Sodium, Flavor (Bubble Gum Flavor), Hydrated Silica Polyethylene Glycol 1450, Purified Water, Saccharin Sodium, Sodium Benzoate, Sodium Lauryl Sulfate, Sorbitol

  • Other Information

    Store between 15º - 35ºC (59º - 95ºF)

  • Questions?

    1-888-396-2739 Monday - Friday 9AM - 5PM EST

  • Label

    5917_BX_MASTER5917 Bubble Fresh Toothpaste with Fluoride

  • Label

    5918_IN_MASTER5918 Bubble Fresh Toothpaste with Fluoride

  • Label

    5919_IN-MASTER5919 Bubble Fresh Toothpaste with Fluoride

  • Label

    5920_BX_MASTER5920 Bubble Fresh Toothpaste with Fluoride

  • INGREDIENTS AND APPEARANCE
    BUBBLE FRESH TOOTHPASTE, WITH FLUORIDE 
    bubble fresh toothpaste, with fluoride paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-191
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION220 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)  
    SORBITOL (UNII: 506T60A25R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    WATER (UNII: 059QF0KO0R)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorBUBBLE GUMImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-191-035 in 1 CASE01/15/2025
    1NDC:67777-191-02144 in 1 BOX
    1NDC:67777-191-0124 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:67777-191-05144 in 1 CASE01/15/2025
    2NDC:67777-191-0442.5 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:67777-191-0772 in 1 CASE01/15/2025
    3NDC:67777-191-0678 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:67777-191-1060 in 1 CASE01/15/2025
    4NDC:67777-191-091 in 1 BOX
    4NDC:67777-191-08130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/15/2025
    Labeler - Dynarex Corporation (008124539)
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