CREST CAVITY PROTECTION REGULAR- sodium fluoride paste, dentifrice 
Procter & Gamble Manufactura, S. de R.L. de C.V.

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Crest ® Cavity Protection

Regular Paste

Drug Facts

Active Ingredient

Sodium fluoride 0.243% (0.15% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect teeth and roots against cavities

Warnings

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.

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, sodium lauryl sulfate, trisodium phosphate, flavor, sodium phosphate, cellulose gum, carbomer, sodium saccharin, titanium dioxide, blue 1

Questions?

1-800-492-7378

Dist. by Procter & Gamble,
Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 161 g Tube Carton

HELPS STOP CAVITIES BEFORE THEY START

Crest®

CAVITY

PROTECTION

ADA

Accepted

American

Dental

Association®

FLUORIDE ANTICAVITY TOOTHPASTE

NET WT 5.7 OZ (161 g)

Regular Paste

Cavity protection

CREST CAVITY PROTECTION  REGULAR
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58933-005
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
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorWINTERGREENImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58933-005-041 in 1 CARTON02/01/2015
1181 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:58933-005-051 in 1 CARTON02/01/2015
2232 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:58933-005-081 in 1 CARTON02/01/2015
3NDC:58933-005-1024 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:58933-005-111 in 1 CARTON02/01/2015
482 g in 1 TUBE; Type 0: Not a Combination Product
5NDC:58933-005-571 in 1 CARTON09/10/2021
5161 g in 1 TUBE; Type 0: Not a Combination Product
6NDC:58933-005-821 in 1 CARTON09/10/2021
6232 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:58933-005-241 in 1 CARTON02/01/2015
768 g in 1 TUBE; Type 0: Not a Combination Product
8NDC:58933-005-8524 g in 1 TUBE; Type 0: Not a Combination Product02/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/01/2015
Labeler - Procter & Gamble Manufactura, S. de R.L. de C.V. (812807550)

Revised: 12/2023
Document Id: 0bd800f0-38b9-4203-e063-6294a90aee0e
Set id: 852889b4-59ba-4592-b4fc-c0127a1ad075
Version: 10
Effective Time: 20231206
 
Procter & Gamble Manufactura, S. de R.L. de C.V.