CREST PRO HEALTH DENSIFY RINSE- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

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Crest Pro Health Densify Rinse

Drug Facts

Active ingredient

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

Purpose

Anticavity

Use

Aids in the prevention of dental cavities

Warning

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, propylene glycol, poloxamer 407, polysorbate 80, flavor, benzoic acid, sucralose, sodium benzoate, phosphoric acid, disodium phosphate

Questions?

1-800-285-9139

DISTR. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 946 mL Bottle Label

Crest®

PRO HEALTH™

ANTICAVITY FLUORIDE RINSE

DENSIFY™

ACTIVELY REBUILDS TOOTH DENSITY

TO EXTEND THE LIFE OF TEETH*

CLEAN MINT

• ALCOHOL FREE

• HELPS PREVENT CAVITIES

• FRESHENS BREATH

IMPORTANT: Read directions for proper use.

946 mL (32 FL OZ)

Crest Pro Health Densify Rinse

CREST PRO HEALTH  DENSIFY RINSE
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-882
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-882-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/01/2022
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 079e140a-b39e-1c2e-e063-6394a90a8491
Set id: d84fb9f9-f2bc-358a-e053-2995a90abf07
Version: 3
Effective Time: 20231013
 
The Procter & Gamble Manufacturing Company