KIDS Crest Advanced Color Changing Toothpaste

KIDS Crest by

Drug Labeling and Warnings

KIDS Crest by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KIDS CREST ADVANCED FLUORIDE ANTICAVITY COLOR CHANGING- sodium monofluorophosphate paste, dentifrice 
The Procter & Gamble Manufacturing Company

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KIDS Crest Advanced Color Changing Toothpaste

Drug Facts

Active ingredient

Sodium monofluorophosphate 0.834% (0.15% w/v fluoride ion)

Purposes

Anticavity toothpaste

Use

helps protect against cavities

Warning

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. of age and older: brush teeth thoroughly after meals or at least twice a day or as directed by a dentist

do not swallow

to minimize swallowing use a pea-sized amount in children under 6 yrs.

supervise children's brushing until good habits are established

children under 2 yrs.: ask a dentist

sorbitol, water, hydrated silica, sodium lauryl sulfate, cellulose gum, flavor, sodium phosphate, trisodium phosphate, mannitol, sodium saccharin, carbomer, silica, titanium dioxide, red 30 lake, blue 1

Questions? 1-800-594-4158

DISTR. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

KIDS Crest Advanced Color Changing

KIDS BRUSH UP TO 2X LONGER

3+ YRS

KID'S Crest ADVANCED

FLUORIDE ANTICAVITY TOOTHPASTE

COLOR CHANGING

I CHANGE BLUE TO PINK WHEN CLEANING

BUBBLEGUM

NET WT 4.2 OZ (119 g)

Kids Color Change

KIDS CREST  ADVANCED FLUORIDE ANTICAVITY COLOR CHANGING
sodium monofluorophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 84126-615
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
SORBITOL (UNII: 506T60A25R)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
SODIUM PHOSPHATE (UNII: SE337SVY37)  
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
D&C RED NO. 30 (UNII: 2S42T2808B)  
MANNITOL (UNII: 3OWL53L36A)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 84126-615-8524 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
2NDC: 84126-615-291 in 1 CARTON01/01/2023
282 g in 1 TUBE; Type 0: Not a Combination Product
3NDC: 84126-615-421 in 1 CARTON01/01/2023
3119 g in 1 TUBE; Type 0: Not a Combination Product
4NDC: 84126-615-044 in 1 CARTON01/01/2023
4119 g in 1 TUBE; Type 0: Not a Combination Product
5NDC: 84126-615-022 in 1 CARTON01/01/2023
5119 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/01/202301/01/2023
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 8/2025
Document Id: 3c5503f0-b202-3733-e063-6394a90a0ec9
Set id: 3ba085fd-dc98-8989-e063-6394a90a9a7c
Version: 2
Effective Time: 20250814
 
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