CREST 3D WHITE LUXE DIAMOND STRONG- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

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Crest ® 3D White Luxe™

Diamond Strong

Drug Facts

Active ingredient

Sodium Fluoride 0.0219% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warning

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

water, glycerin, propylene glycol, hydrogen peroxide, poloxamer 407, flavor, sodium saccharin, phosphoric acid, sucralose, disodium phosphate

Questions?

1-800-285-9139

DISTR. BY PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

WITH FLUORIDE
ALCOHOL FREE

Crest
®

3D WHITE


ANTICAVITY FLUORIDE MOUTHWASH

DIAMOND STRONG

FROM THE MAKERS OF WHITESTRIPS ®

WINTERMINT

IMPORTANT: Read directions for proper use.

946 mL

(32 FL OZ) Label

CREST 3D WHITE LUXE  DIAMOND STRONG
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-862
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
Product Characteristics
Colorwhite (Clear) Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-862-01473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/19/2015
2NDC:37000-862-02946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/19/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/19/2015
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 079e21a0-89da-1f42-e063-6394a90aa9d6
Set id: c1420129-5460-4900-ac9a-356d2d7c60a2
Version: 7
Effective Time: 20231013
 
The Procter & Gamble Manufacturing Company