WHITE GLO PROFESSIONAL CHOICE TWIN PACK- sodium fluoride 
WHITE GLO USA INC

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White Glo Professional Choice Twin Pack toothpaste

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

Calcium carbonate, water, sorbitol, glycerin, hydrated silica, sodium lauryl sulfate, flavor, sodium saccharin, sodium silicate, trisodium phosphate, cellulose gum, hydroxyethylcellulose, rosa canina (rose hip) fruit oil

Questions or comments

For customer enquiries, please contact: customer.service@whiteglo.com White Glo USA INC. 42 West Campbell Avenue, Third Floor Campbell, California 9500. www.whiteglo.com

Package Labeling:

Outer Package
Inner Package
WHITE GLO PROFESSIONAL CHOICE TWIN PACK 
sodium fluoride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73656-024
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-024-001 in 1 BOX10/19/2023
11 in 1 KIT
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 12 TUBE 300 g
Part 1 of 1
WHITE GLO PROFESSIONAL CHOICE 
sodium fluoride paste, dentifrice
Product Information
Item Code (Source)NDC:73656-025
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CALCIUM CARBONATE (UNII: H0G9379FGK)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM SILICATE (UNII: IJF18F77L3)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-025-00150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02110/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02110/19/2023
Labeler - WHITE GLO USA INC (117345666)

Revised: 12/2023
Document Id: 0c914bf5-accd-5312-e063-6394a90a38ce
Set id: 0c913e38-e655-7208-e063-6294a90a58c9
Version: 1
Effective Time: 20231215
 
WHITE GLO USA INC