CREST 3D WHITE BRILLIANCE LUMINOUS PURPLE- sodium fluoride paste, dentifrice

Crest by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Sodium fluoride 0.243% (0.15% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warning

Keep out of reach of children under 6 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 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
• do not swallow
• to minimize swallowing use a pea-sized amount in children under 6
• supervise children's brushing until good habits are established
• children under 2 yrs.: ask a dentist

Inactive ingredients

glycerin, hydrated silica, sodium hexametaphosphate, water, PEG-6, flavor, sodium
lauryl sulfate, cocamidopropyl betaine, trisodium phosphate, sodium saccharin, PVP, carrageenan, xanthan gum, sucralose, mica, titanium dioxide, red 40, blue 1

Questions?

1-800-492-7378

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 99 g Tube Carton

24 HR ACTIVE STAIN PREVENTION*

CREST

3D WHTE

NET WT

3.5 OZ (99 g)

FLUORIDE ANTICAVITY TOOTHPASTE

BRILLIANCE

OUR PURPLE TOOTHPASTE REMOVES

100% MORE STAINS**

WHITER TEETH IN 3 DAYS

LUMINOUS PURPLE

INGREDIENTS AND APPEARANCE

CREST  3D WHITE BRILLIANCE LUMINOUS PURPLE
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-787
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.6 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CARRAGEENAN (UNII: 5C69YCD2YJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
XANTHAN GUM (UNII: TTV12P4NEE)
GLYCERIN (UNII: PDC6A3C0OX)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-787-85	1 in 1 CARTON	06/15/2022
1		24 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69423-787-46	1 in 1 CARTON	06/15/2022
2		131 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 69423-787-35	1 in 1 CARTON	06/15/2022
3		99 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 69423-787-34	3 in 1 CARTON	06/15/2022
4		130 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	06/15/2022

Labeler - The Procter & Gamble Manufacturing Company (004238200)