Crest 3D White Enamel Protect Toothpaste

Crest 3D White by

Drug Labeling and Warnings

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

Drug Details [pdf]

CREST 3D WHITE ENAMEL PROTECT- sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest 3D White Enamel Protect Toothpaste

Drug Facts

Active ingredient

Sodium fluoride 0.243% (0.16% 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, carrageenan, sodium saccharin, PEG-20M, xanthan gum, sucralose, mica, titanium dioxide

Questions?

1-800-492-7378

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 85 g Tube Carton

Crest

3D WHITE
FLUORIDE ANTICAVITY TOOTHPASTE

CLINICALLY PROVEN

WHITENING INGREDIENTS

WHITER TEETH

IN 3 DAYS*

Up to 100% STAIN REMOVAL*

ENAMEL PROTECT

NET WT

3.0 OZ (85 g)

ENAMEL SAFE

CREST 3D WHITE  ENAMEL PROTECT
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-854
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
XANTHAN GUM (UNII: TTV12P4NEE)
SUCRALOSE (UNII: 96K6UQ3ZD4)
CARRAGEENAN (UNII: 5C69YCD2YJ)
HEXASODIUM HEXAMETAPHOSPHATE (UNII: N40N91DW96)
POLYETHYLENE OXIDE 900000 (UNII: 16P9295IIL)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

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: 69423-854-30	1 in 1 CARTON	01/11/2022
1		85 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	01/11/2022	06/01/2025

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 7/2025

Document Id: 3a0f94f8-18ea-6952-e063-6294a90aaec0

34390-5

Set id: d4ec0f3e-5c33-0229-e053-2995a90a57b0

Version: 7

Effective Time: 20250716

 

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