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

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Crest ® 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 lauryl sulfate, sodium hydroxide, flavor, xanthan gum, sodium saccharin, cellulose gum, carbomer, titanium dioxide, blue 1

Questions?

1-800-492-7378

Dist. by Procter & Gamble, Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 161 g Tube Carton

HELPS PREVENT TARTAR & CAVITIES

Crest®

ADA

Accepted


American

Dental

Association ®

FLUORIDE ANTICAVITY TOOTHPASTE

NET WT 5.7 OZ (161 g)

TARTAR
PROTECTION

Regular Paste

008

CREST TARTAR PROTECTION 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-008
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 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)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorCINNAMONImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-008-021 in 1 CARTON10/01/202107/13/2023
182 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:37000-008-031 in 1 CARTON10/01/202107/13/2023
2130 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:37000-008-041 in 1 CARTON10/01/202107/13/2023
3181 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:37000-008-241 in 1 CARTON09/01/2019
468 g in 1 TUBE; Type 0: Not a Combination Product
5NDC:37000-008-421 in 1 CARTON09/01/2019
5119 g in 1 TUBE; Type 0: Not a Combination Product
6NDC:37000-008-571 in 1 CARTON09/01/2019
6161 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02111/06/1992
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 07ec5d59-1e2f-896e-e063-6294a90afd04
Set id: 85477763-1db5-482f-90e5-e71f5c1b4765
Version: 10
Effective Time: 20231017
 
The Procter & Gamble Manufacturing Company