KIDS CREST CAVITY PROTECTION SPARKLE FUN- sodium fluoride paste, dentifrice

Kids Crest Cavity Protection by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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)

INGREDIENTS AND APPEARANCE

KIDS CREST CAVITY PROTECTION  SPARKLE FUN
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-049
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM PHOSPHATE (UNII: SE337SVY37)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37000-049-03	2.5 g in 1 POUCH; Type 0: Not a Combination Product	09/05/2002
2	NDC: 37000-049-01	1 in 1 CARTON	09/05/2002
2		24 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 37000-049-04	1 in 1 CARTON	09/05/2002	12/19/2016
3		77 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 37000-049-02	1 in 1 CARTON	09/05/2002
4		130 g in 1 TUBE; Type 0: Not a Combination Product
5	NDC: 37000-049-06	170 g in 1 BOTTLE; Type 0: Not a Combination Product	09/05/2002	12/01/2018
6	NDC: 37000-049-05	1 in 1 CARTON	09/05/2002	06/14/2019
6		76 g in 1 TUBE; Type 0: Not a Combination Product
7	NDC: 37000-049-42	119 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2017
8	NDC: 37000-049-92	2 in 1 CELLO PACK	09/05/2002
8		1 in 1 CARTON
8		130 g in 1 TUBE; Type 0: Not a Combination Product
9	NDC: 37000-049-22	1 in 1 CARTON	01/07/2019
9		62 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 final	part355	09/05/2002

Labeler - The Procter & Gamble Manufacturing Company (004238200)