CREST PRO-HEALTH PRO ACTIVE DEFENSE WHOLE MOUTH PROTECTION- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

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Crest ®
Pro-Health
Pro Active Defense Whole Mouth Protection

Drug Facts

Active ingredient

Sodium Fluoride 0.02% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warnings

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

Directions

Inactive ingredients

water, glycerin, flavor, poloxamer 407, cetylpyridinium chloride, sodium saccharin, phosphoric acid, methylparaben, sucralose, propylparaben, disodium phosphate, yellow 6, green 3

Questions?

1–800–285–9139

DISTR. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 1000 mL Bottle Label

ALCOHOL FREE

+FLUORIDE

Crest ®

PRO-HEALTH™

ANTICAVITY FLUORIDE MOUTHWASH

PRO / ACTIVE DEFENSE
Proactively SHIELDS & PROTECTS Against

IMPORTANT: Read directions for proper use.

Bad Breath

Enamel Loss

Cavities

1L (33.8 FL OZ)

958

CREST PRO-HEALTH  PRO ACTIVE DEFENSE WHOLE MOUTH PROTECTION
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-958
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION2.2 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Product Characteristics
ColorturquoiseScore    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-958-011000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/31/2020
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 06fd57fc-7f75-28bd-e063-6394a90a17c5
Set id: 9fe5a5b1-3e3b-1f28-e053-2995a90a1852
Version: 4
Effective Time: 20231005
 
The Procter & Gamble Manufacturing Company