CREST 3D WHITE ADVANCED- sodium monofluorophosphate paste, dentifrice

Crest 3D White Advanced by

Drug Labeling and Warnings

Crest 3D White Advanced by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Sodium monofluorophosphate 1.14%

(0.17% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect against cavities

WARNINGS

Warning

Keep out of reach of children under 12 yrs. 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 12 yrs. & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.
• do not swallow
• children under 12 yrs.: ask a dentist

Inactive ingredients

water, glycerin, calcium pyrophosphate, hydrogen peroxide (2.5% w/v), sodium lauryl sulfate, flavor, polyacrylate crosspolymer-6, cetearyl alcohol, disodium pyrophosphate, tetrasodium pyrophosphate, sucralose

Questions?

1-800-492-7378

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

Crest 3D White Ultra White 85g tube in carton

Crest

3D WHITE

FLUORIDE ANTICAVITY TOOTHPASTE

ADVANCED HYDROGEN PEROXIDE

2.5%

WHITENS* AND DEEPLY CLEANS

*BY REMOVING SURFACE STAINS

FRESH MINT

ENAMEL SAFE WHITENING

NET WT 3.0 OZ (85 g)

INGREDIENTS AND APPEARANCE

CREST 3D WHITE ADVANCED 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-752
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.7 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-752-30	1 in 1 CARTON	01/10/2023
1		85 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69423-752-23	1 in 1 CARTON	01/10/2023
2		65 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	M022	01/10/2023

Labeler - The Procter & Gamble Manufacturing Company (004238200)