CREST COMPLETE MULTI-BENEFIT EXTRA WHITENING WITH TARTAR PROTECTION- sodium fluoride paste, dentifrice

Crest Complete Multi-Benefit Extra Whitening by

Drug Labeling and Warnings

Crest Complete Multi-Benefit Extra Whitening 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% (0.16% 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, disodium pyrophosphate, sodium lauryl sulfate, sodium hydroxide, flavor, xanthan gum, sodium saccharin, carbomer, carnauba wax, titanium dioxide, blue 1, yellow 5

Questions?

1-800-699-3974

SPL UNCLASSIFIED SECTION

Dist. by Procter & Gamble,
Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 175 g Tube Carton

Fights Cavities + Whiter Teeth in One Tube*

Crest®
complete
MULTI-BENEFIT ™

FLUORIDE TOOTHPASTE

NET WT 6.2 OZ (175 g)

EXTRA
WHITENING
with tartar protection

clean mint

INGREDIENTS AND APPEARANCE

CREST COMPLETE MULTI-BENEFIT EXTRA WHITENING  WITH TARTAR PROTECTION
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-829
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.6 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
XANTHAN GUM (UNII: TTV12P4NEE)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
CARNAUBA WAX (UNII: R12CBM0EIZ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color	green	Score
Shape		Size
Flavor	PEPPERMINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37000-829-04	1 in 1 CARTON	07/01/2011	12/31/2014
1		124 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 37000-829-05	164 g in 1 TUBE; Type 0: Not a Combination Product	07/01/2011	10/31/2012
3	NDC: 37000-829-06	1 in 1 CARTON	07/01/2011
3		175 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 37000-829-08	1 in 1 CARTON	07/01/2011	11/05/2017
4		226 g in 1 TUBE; Type 0: Not a Combination Product
5	NDC: 37000-829-01	1 in 1 CARTON	07/01/2011
5		45 g in 1 TUBE; Type 0: Not a Combination Product
6	NDC: 37000-829-12	2 in 1 CARTON	07/01/2011
6		175 g in 1 TUBE; Type 0: Not a Combination Product
7	NDC: 37000-829-99	2 in 1 CARTON	01/01/2019
7		153 g in 1 TUBE; Type 0: Not a Combination Product
8	NDC: 37000-829-54	1 in 1 CARTON	01/01/2019
8		153 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	07/01/2011	09/03/2020

Labeler - The Procter & Gamble Manufacturing Company (004238200)