WHITE GLO CHARCOAL BAKING SODA MAXIMUM WHITE FLUORIDE ANTICAVITY- sodium monofluorophosphate kit

Drug Labeling and Warnings

Drug Details [pdf]

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, Glycerin, Sodium Lauryl Sulfate, Flavor, Sodium Bicarbonate, Cellulose Gum, Chondrus Crispus Extract, Sodium Saccharin, Sodium Benzoate, Tetrasodium Pyrophosphate, Rose Hip Oil, Charcoal Powder, Titanium Dioxide.

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:

INGREDIENTS AND APPEARANCE

WHITE GLO CHARCOAL BAKING SODA MAXIMUM WHITE FLUORIDE ANTICAVITY 
sodium monofluorophosphate kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73656-041

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73656-041-00	1 in 1 KIT	03/31/2025

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	2 TUBE	300 g

Part 1 of 1

WHITE GLO MAXIMUM WHITE CHARCOAL 
sodium monofluorophosphate paste, dentifrice

Product Information
Item Code (Source)	NDC: 73656-014
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73656-014-00	1 in 1 CARTON
1		150 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	03/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	03/31/2025

Labeler - White Glo USA Inc (117345666)

Registrant - White Glo USA Inc (117345666)