KIDS CREST CAVITY PROTECTION- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Kid's Crest ®

Cavity Protection

Drug Facts

Active ingredient

Sodium Fluoride 0.022% (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

  • Adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste.
  • To dispense 10 mL dose: Remove cap and squeeze the front and back of the bottle (not the sides) to fill the reservoir. Allow excess liquid to drain back into the bottle. Pour out the dose.
  • Vigorously swish the 10 mL of rinse between your teeth for 1 minute and then spit out.
  • Do not swallow the rinse.
  • Do not eat or drink for 30 minutes after rinsing.
  • Instruct children under 12 years of age in good rinsing habits (to minimize swallowing).
  • Supervise children as necessary until capable of using without supervision.
  • Children under 6 years of age: Consult a dentist or doctor.

Inactive ingredients

water, glycerin, propylene glycol, polysorbate 80, flavor, sodium saccharin, phosphoric acid, methylparaben, propylparaben, disodium phosphate, red 33, red 40.

Questions?

1-800-285-9139

Dist. by Procter & Gamble,
Cincinnati OH 45202

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

ADA
Accepted
American
Dental
Association ®

ALCOHOL FREE

KID'S
Crest ®

ANTI-CAVITY FLUORIDE RINSE

PROTECTS AGAINST CAVITIES
STRENGTHENS TEETH
FRESHENS BREATH

92121035

CAVITY
PROTECTION

IMPORTANT: READ DIRECTIONS FOR PROPER USE.

500 mL
(16.9 FL OZ)

SPARKLE FUN BERRY

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label
KIDS CREST  CAVITY PROTECTION
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-833
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Product Characteristics
ColorpinkScore    
ShapeSize
FlavorSTRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-833-01500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/23/201206/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35507/23/201206/01/2017
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 9/2016
Document Id: 3dabab08-39c0-2313-e054-00144ff88e88
Set id: 20d9a877-d9da-4468-b197-a01ae984c60f
Version: 2
Effective Time: 20160929
 
The Procter & Gamble Manufacturing Company