KIDS CREST STRAWBERRY RUSH- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

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Kid's Crest Strawberry Rush Anti Cavity Fluoride 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, polysorbate 80, benzoic acid, flavor, sucralose, sodium benzoate, phosphoric acid, disodium phosphate, red 33

Questions?

1-800-285-9139

DISTR. BY PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

Kid's Crest Strawberry Rush Rinse

ALCOHOL FREE

KID'S

Crest®



ANTICAVITY

FLUORIDE RINSE

STRAWBERRY RUSH

IMPORTANT:

Read directions

for proper use.



REACHES WHERE BRUSHING MAY MISS

500 mL

(16.9 FL OZ)

KIDS CREST  STRAWBERRY RUSH
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-895
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
BENZOIC ACID (UNII: 8SKN0B0MIM)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Product Characteristics
ColorpinkScore    
ShapeSize
FlavorSTRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-895-16500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02107/01/2022
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 07ea098f-0251-21d5-e063-6294a90a3be5
Set id: eb7a5698-754c-4e46-e053-2a95a90a57b4
Version: 2
Effective Time: 20231017
 
The Procter & Gamble Manufacturing Company