ADVANCE WHITE BREATH FRESHENING TARTAR CONTROL- sodium fluoride gel, dentifrice

Advance White by

Drug Labeling and Warnings

Advance White by is a Otc medication manufactured, distributed, or labeled by Church & Dwight Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients        
Sodium fluoride (0.24%)

PURPOSE

Purpose
Anticavity toothpaste

INDICATIONS & USAGE

Use    aids in the prevention of dental decay   

KEEP OUT OF REACH OF CHILDREN

Warning

Keep out of reach of children under 6 years of age.

WARNINGS

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions           do not swallow    supervise children as necessary until capable of using without supervision

adults and children 2 years and older           brush teeth throughly after meals or at least twice a day, or use as directed by a dentist or physician
children under 6 years                                    instruct in good brushing and rinsing habits (to minimize swallowing)
children under 2 years                                    consult a dentist or physician

INACTIVE INGREDIENT

Inactive ingredients   Sorbitol, Sodium Bicarbonate (baking soda), Water, Hydrated Silica, Glycerin, Tetrasodium Pyrophosphate, Flavor, Sodium Lauryl Sulfate, Sodium Saccharin, Sodium Lauroyl Sarcosinate, Cellulose Gum, Blue 1, Yellow 5.

QUESTIONS

Questions or comments?  Call 1-800-786-5135 Monday-Friday 9am-5pm ET or visit www.myoralcare.com

Principal Display Panel

ARM AND HAMMER The Standard of Purity

Fluoride Anti-Cavity Toothpaste TARTAR CONTROL FROSTED MINT FLAVOR

ADVANCE WHITE Gel

Breath Freshening Baking Soda and Frosted Mint

NET WT. 6.0OZ. (170g)

Carton image

INGREDIENTS AND APPEARANCE

ADVANCE WHITE  BREATH FRESHENING TARTAR CONTROL
sodium fluoride gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10237-657
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	2.4 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color	green	Score
Shape		Size
Flavor	MINT (Frosted Mint Flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10237-657-60	1 in 1 CARTON	01/29/2012	11/11/2022
1		170 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 final	part355	01/29/2012	11/11/2022

Labeler - Church & Dwight Co., Inc. (001211952)

Establishment
Name	Address	ID/FEI	Business Operations
Church & Dwight Co., Inc.		043690812	manufacture(10237-657)