CREST KIDS ADVANCED COLOR CHANGING- sodium monofluorophosphate paste, dentifrice

Crest Kids Advanced Color Changing by

Drug Labeling and Warnings

Crest Kids Advanced Color Changing by is a Otc medication manufactured, distributed, or labeled by Procter & Gamble Manufactura, S de R.L. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

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

Purpose

Anticavity toothpaste

Use

helps protect teeth and roots 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.

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 ingredients

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

SPL UNCLASSIFIED SECTION

DISTR. BY PROCTER & GAMBLE

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - Crest Kids 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

CREST KIDS ADVANCED COLOR CHANGING 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58933-012
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
D&C RED NO. 30 (UNII: 2S42T2808B)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM PHOSPHATE (UNII: SE337SVY37)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
MANNITOL (UNII: 3OWL53L36A)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SORBITOL (UNII: 506T60A25R)
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

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: 58933-012-85	1 in 1 CARTON	01/01/2023
1		24 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 58933-012-42	1 in 1 CARTON	01/01/2023
2		119 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 58933-012-29	1 in 1 CARTON	01/01/2023
3		82 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	M022	01/01/2023

Labeler - Procter & Gamble Manufactura, S de R.L. de C.V. (812807550)