WHITE GLO ADVANTAGE ANTICAVITY FLUORIDE PURPLE- sodium monofluorophosphate paste 
WHITE GLO USA INC

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White Glo Advantage Anticavity Fluoride Purple 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, Aqua, Glycerin, Sorbitol, Hydrated Silica, Sodium Lauryl Sulfate, Aroma, Sodium Monofluorophosphate, Cellulose Gum, Mentholum, Hydroxyethylcellulose, Sodium Silicate, Sodium Saccharin, Trisodium Phosphate, D&C Red No.33, FD&C Blue No.1

Questions or comments

For customer enquiries, please contact: customer.service@whiteglo.com White Glo USA INC. 42 West Campbell Avenue, Third Floor, Campbell, California, 95008. www.whiteglo.com

Package Labeling:

Label.jpgTube Label

WHITE GLO ADVANTAGE ANTICAVITY FLUORIDE PURPLE 
sodium monofluorophosphate paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73656-026
Route of AdministrationTOPICAL
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
CALCIUM CARBONATE (UNII: H0G9379FGK)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITOL (UNII: 506T60A25R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
SODIUM SILICATE (UNII: IJF18F77L3)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73656-026-001 in 1 BOX04/20/2024
1100 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02104/20/2024
Labeler - WHITE GLO USA INC (117345666)

Revised: 5/2024
Document Id: 187f5e57-ee57-38d4-e063-6394a90ac42b
Set id: b25aa35b-98ce-4605-a7b1-8c2fe476e1a8
Version: 1
Effective Time: 20240515
 
WHITE GLO USA INC