Label: WHITE GLO INSTANT WHITE BLUE FOAM OPTICAL ENHANCERS FLUORIDE ANTICAVITY VALUE 2 PACK AND TOOTHBRUSH- sodium monofluorophosphate kit

  • NDC Code(s): 73656-028-00, 73656-029-00
  • Packager: WHITE GLO USA INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 17, 2024

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

View All Sections
  • Drug Facts

  • Active ingredient

    Sodium Monofluorophosphate 0.76% (0.1% W/V Fluoride ion).

    Purpose

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • Warnings

    Keep out of reach of children

    under 6 years of age.

    If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

     Adults and children 2 years of age & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
     Children under 6 years of age: Instruct in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.

    Children under 2 years of age: Consult a dentist or doctor.

  • Other information

    • Store in a cool place, below 86° F, away from heat
    • Do not use if quality seal is broken or missing
  • Inactive ingredients

    Sorbitol, Hydrated Silica, Water (Aqua), Sodium Lauryl Sulfate, Polyethylene Glycol 400, Flavour, Xylitol, Sodium Benzoate, Trisodium Phosphate, Cellulose Gum, Mica, FD&C Blue No. 1.

  • Questions or comments

    For customer enquiries, please contact: customer.service@whiteglo.com

  • Package Labeling:

    LabelLabel2

  • INGREDIENTS AND APPEARANCE
    WHITE GLO INSTANT WHITE BLUE FOAM OPTICAL ENHANCERS FLUORIDE ANTICAVITY VALUE 2 PACK AND TOOTHBRUSH 
    sodium monofluorophosphate kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73656-028
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73656-028-001 in 1 KIT05/30/2024
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 12 TUBE 300 g
    Part 1 of 1
    BLUE INSTANT WHITE WITH BLUE FOAM OPTICAL ENHANCERS FLUORIDE ANTICAVITY 
    sodium monofluorophosphate paste, dentifrice
    Product Information
    Item Code (Source)NDC:73656-029
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION7.6 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    XYLITOL (UNII: VCQ006KQ1E)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    MICA (UNII: V8A1AW0880)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73656-029-00150 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02105/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02105/30/2024
    Labeler - WHITE GLO USA INC (117345666)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!