CREST PLUS TARTAR PROTECTION- sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest Plus Tartar Protection

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

sorbitol, water, hydrated silica, disodium pyrophosphate, sodium
hydroxide, sodium lauryl sulfate, flavor, xanthan gum, sodium saccharin,
carbomer, cellulose gum, sodium benzoate, potassium sorbate, titanium
dioxide

Questions?

1-800-492-7378

Dist. by Procter & Gamble, Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 161 g Tube Carton

ADA
Accepted
American
Dental
Association

Crest plus

FLUORIDE ANTICAVITY TOOTHPASTE
NET WT 4.2 OZ (119 g)

TARTAR
PROTECTION

HELPS PREVENT TARTAR & CAVITIES

Regular Paste

LABEL

CREST PLUS TARTAR PROTECTION 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-817
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-817-241 in 1 CARTON11/13/2023
168 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:69423-817-421 in 1 CARTON11/13/2023
2119 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:69423-817-571 in 1 CARTON11/13/2023
3161 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02111/13/2023
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 11/2023
Document Id: 08767979-343e-0003-e063-6394a90ad89f
Set id: 08767b0f-ed6e-8d32-e063-6294a90a10cd
Version: 1
Effective Time: 20231113
 
The Procter & Gamble Manufacturing Company