CREST 3D WHITE ADVANCED LUMINOUS MINT- sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest 3D White Advanced Luminous Mint

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

Inactive ingredients

water, sorbitol, hydrated silica, disodium
pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, cellulose gum,
sodium saccharin, carbomer, polysorbate 80, mica, titanium dioxide, blue 1

Questions?

1-800-492-7378

DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 104 g Tube Carton

INTENSE WHITENING

CREST

3D WHITE

ADVANCED

LUMINOUS MINT

net wt 3.7 oz (104 g)

fluoride anticavity toothpaste

ENAMEL SAFE WHITENING

REMOVES 90% MORE SURFACE STAINS*

STARTS WHITENING AFTER 1 BRUSH

artwork

CREST 3D WHITE  ADVANCED LUMINOUS MINT
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-769
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
MICA (UNII: V8A1AW0880)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-769-371 in 1 CARTON08/01/2021
1104 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02110/11/2020
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 078559ad-26e5-f477-e063-6394a90a959a
Set id: f5c82742-fb27-62a2-e053-2a95a90aa7c4
Version: 3
Effective Time: 20231012
 
The Procter & Gamble Manufacturing Company