WHITE GLO INSTANT WHITE- sodium monofluorophosphate 
WHITE GLO USA INC

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White Glo Toothpaste Instant White + Toothbrush

Drug Facts

Active ingredient

Sodium monofluorophosphate 0.76%(0.1% W/V fluoride ion)

Purpose

Anticavity toothpaste

Use

helps pretect against cavities

Warnings

Keep out of reach of children

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center rightaway. under 6 years of age.

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, Flavor, Xylitol, Sodium Benzoate, Tetrasodium Pyrophosphate, Cellulose Gum, Mica, FD&C Blue No.1

Questions or comments

For customer enquiries, please contact:customer.service@whiteglo.com White Glo USA INC. 25 Suffolk Court, Hauppauge, NY, 11788 USA. www.whiteglo.com

Package Labeling:

Outer Package2Inner Package2

WHITE GLO INSTANT WHITE 
sodium monofluorophosphate kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73656-015
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-015-001 in 1 KIT11/01/2021
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 150 g
Part 1 of 1
WHITE GLO INSTANT WHITE 
sodium monofluorophosphate paste, dentifrice
Product Information
Item Code (Source)NDC:73656-016
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.001 mg  in 100 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)  
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
MICA (UNII: V8A1AW0880)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-016-001 in 1 CARTON
1150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02111/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02111/01/2021
Labeler - WHITE GLO USA INC (117345666)

Revised: 10/2023
Document Id: 08ac4020-ee76-2fcd-e063-6394a90aaee2
Set id: ce4f0f8f-46f0-b4e6-e053-2a95a90af6c6
Version: 3
Effective Time: 20231027
 
WHITE GLO USA INC