WHITE GLO INSTANT WHITE BLUE FOAM OPTICAL ENHANCERS FLUORIDE ANTICAVITY VALUE 2 PACK AND TOOTHBRUSH- sodium monofluorophosphate 
WHITE GLO USA INC

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White Glo Instant White Blue Foam Optical Enhancers Fluoride Anticavity Toothpaste Value 2 pack and Toothbrush

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

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

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)

Revised: 6/2024
Document Id: 1b1bba9b-bde2-2d81-e063-6294a90a0c23
Set id: 7c15eedb-d4ca-4fc1-8a1e-6f9cad0cc126
Version: 1
Effective Time: 20240617
 
WHITE GLO USA INC