CREST PREMIUM PLUS SCOPE DUAL BLAST ACTIVE FOAM- sodium fluoride paste, dentifrice

Crest Premium Plus by

Drug Labeling and Warnings

Crest Premium Plus 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, disodium pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, alcohol (0.7%), xanthan gum, sodium saccharin, glycerin, cellulose gum, carbomer, polysorbate 80, sodium benzoate, cetylpyridinium chloride, benzoic acid, titanium dioxide, blue 1

Questions?

1-800-492-7378

SPL UNCLASSIFIED SECTION

Dist. by Procter & Gamble,Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 204 g Tube Carton

Crest

plus

PREMIUM

NET WT/PESO NETO 7.2OZ (204 g)

ANTICAVITY FLUORIDE TOOTHPASTE

PASTA DENTAL ANTICARIES CON FLUORURO

ACTIVE FOAM

+WHITENING
scope ®
DUALBLAST®

BLASTS AWAY 99.9% OF BAD BREATH GERMS*

intense mint

menta intensa

INGREDIENTS AND APPEARANCE

CREST PREMIUM PLUS  SCOPE DUAL BLAST ACTIVE FOAM
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37000-990
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
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ALCOHOL (UNII: 3K9958V90M)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
BENZOIC ACID (UNII: 8SKN0B0MIM)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
XANTHAN GUM (UNII: TTV12P4NEE)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37000-990-72	1 in 1 CARTON	01/01/2021
1		204 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 37000-990-52	1 in 1 CARTON	01/01/2021
2		147 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 37000-990-03	3 in 1 CELLO PACK	01/01/2021	07/13/2023
3		1 in 1 CARTON
3		147 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 37000-990-35	3 in 1 CARTON	01/01/2021
4		147 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	01/01/2021

Labeler - The Procter & Gamble Manufacturing Company (004238200)