Medication Guide App

Kids Crest Cavity Protection Sparkle Fun

Dosage form: paste, dentifrice
Ingredients: Sodium Fluoride 2.43mg in 1g
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-049

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.

Kid's
Crest®
Cavity Protection

Drug Facts

Active ingredient

Sodium fluoride 0.243% (0.15% w/v fluoride ion)

Purpose

Anticavity toothpaste

Use

helps protect against cavities

Warnings

Keep out of reach of children under 6 yrs. of age.

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

Directions
  • adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
    • do not swallow
    • to minimize swallowing use a pea-sized amount in children under 6
    • supervise children's brushing until good habits are established
  • children under 2 yrs.: ask a dentist

Inactive ingredients

sorbitol, water, hydrated silica, sodium lauryl sulfate, trisodium phosphate, sodium phosphate, cellulose gum, flavor, sodium saccharin, carbomer, mica, titanium dioxide, blue 1

Questions?

1-800-492-7378

PRINCIPAL DISPLAY PANEL - 76.5 g Tube Carton

KID'S
Crest®

CAVITY
PROTECTION

ADA
Accepted

American
Dental
Association®

FLUORIDE ANTICAVITY
TOOTHPASTE

SPARKLE FUN
FLAVOR

NET WT 2.7 OZ (76.5 g)

KIDS CREST CAVITY PROTECTION   SPARKLE FUN
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-049
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Fluoride (Fluoride Ion) Sodium Fluoride2.43 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
sorbitol 
water 
hydrated silica 
sodium lauryl sulfate 
sodium phosphate 
carboxymethylcellulose sodium 
saccharin sodium dihydrate 
mica 
titanium dioxide 
FD&C blue no. 1 
Packaging
#Item CodePackage Description
1NDC:37000-049-032.5 g in 1 POUCH
2NDC:37000-049-011 TUBE (TUBE) in 1 CARTON
224 g in 1 TUBE
3NDC:37000-049-041 TUBE (TUBE) in 1 CARTON
377 g in 1 TUBE
4NDC:37000-049-021 TUBE (TUBE) in 1 CARTON
4130 g in 1 TUBE
5NDC:37000-049-06170 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35509/05/2002
Labeler - Procter & Gamble Manufacturing Company (004238200)

Revised: 01/2012
 
Procter & Gamble Manufacturing Company

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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