KIDS CREST ADVANCED FLUORIDE ANTICAVITY COLOR CHANGING- stannous fluoride paste, dentifrice

KIDS Crest by

Drug Labeling and Warnings

KIDS Crest by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company, Procter & Gamble Manufacturing México, S. de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INACTIVE INGREDIENT

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

Questions? 1-800-594-4158

SPL UNCLASSIFIED SECTION

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)

INGREDIENTS AND APPEARANCE

KIDS CREST  ADVANCED FLUORIDE ANTICAVITY COLOR CHANGING
stannous fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-896
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.6 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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
Color	blue	Score
Shape		Size
Flavor	BUBBLE GUM	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-896-85	24 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2023
2	NDC: 69423-896-29	1 in 1 CARTON	01/01/2023
2		82 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 69423-896-42	1 in 1 CARTON	01/01/2023
3		119 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 69423-896-04	4 in 1 CARTON	01/01/2023
4		119 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	01/01/2023

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Establishment
Name	Address	ID/FEI	Business Operations
Procter & Gamble Manufacturing México, S. de R.L. de C.V.		812807550	manufacture(69423-896)