CREST PRO-HEALTH SENSITIVITY RELIEF- sodium fluoride and potassium nitrate paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Crest Pro-Health Advanced Sensitivity plus Scope

Drug Facts

Active ingredientsPurpose
Potassium nitrate 5%Toothpaste for sensitive teeth
Sodium fluoride 0.243% (0.14% w/v fluoride ion)Toothpaste for cavity prevention

Uses

Warnings

When using this productdo not use longer than four weeks unless recommended by a dentist.

Stop use and ask a dentist ifproblem lasts or gets worse. Sensitive teeth may indicate a serious problem that may need prompt care.

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

Directions

Inactive ingredients

water, hydrated silica, glycerin, sorbitol, sodium lauryl sulfate,
trisodium phosphate, flavor, cellulose gum, alcohol (0.7%), sodium saccharin, xanthan
gum, polysorbate 80, cetylpyridinium chloride, titanium dioxide, blue 1

Questions?

1-800-492-7378

Dist. by Procter & Gamble, Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 170 g Tube Carton

Crest

PRO-HEALTH

NET WT

5.1 0Z (144 g)

TOOTHPASTE FOR SENSITIVE TEETH AND CAVITY PROTECTION

DENTIST DESIGNED

CLINICALLY PROVEN

+ WHITENING

SENSITIVITY RELIEF

Maximum strength** sensitivity relief

MINTY FRESH SCOPE

label

CREST PRO-HEALTH  SENSITIVITY RELIEF
sodium fluoride and potassium nitrate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-639
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE50 mg  in 1 g
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.4 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CELLULOSE GUM (UNII: K679OBS311)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITOL (UNII: 506T60A25R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
ALCOHOL (UNII: 3K9958V90M)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84126-639-511 in 1 CARTON01/06/2026
1144 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:84126-639-052 in 1 CARTON01/06/2026
2144 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/06/2026
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 4/2026
Document Id: 4f1d60b7-cd30-3192-e063-6294a90aa82a
Set id: 4f1d62ae-653e-3046-e063-6294a90abbf8
Version: 1
Effective Time: 20260410
 
The Procter & Gamble Manufacturing Company