OTC Medication Information: Crest Complete Multi Benefit Whitening Plus Scope Minty Fresh Gel

CREST COMPLETE MULTI BENEFIT WHITENING PLUS SCOPE MINTY FRESH GEL- sodium fluoride paste, dentifrice
Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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, carbomer, cellulose gum, polysorbate 80, sodium benzoate, cetylpyridinium chloride, benzoic acid, blue 1, yellow 5

Questions?

1-800-492-7378

Dist. by Procter & Gamble,
Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL — 119 g pump label

Crest ®

complete

MULTI-BENEFIT

FLUORIDE ANTICAVITY TOOTHPASTE

WHITENING+

scope®

KILLS MILLIONS OF

BAD BREATH GERMS*

MINTY

FRESH GEL

NET WT 4.2 OZ (119 g)

494
(click image for full-size original)
CREST COMPLETE MULTI BENEFIT WHITENING PLUS SCOPE MINTY FRESH GEL
sodium fluoride paste, dentifrice
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-494
Route of Administration DENTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION 1.5 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
SODIUM ACID PYROPHOSPHATE
CARBOXYMETHYLCELLULOSE SODIUM
SODIUM HYDROXIDE
ALCOHOL
XANTHAN GUM
POLYSORBATE 80
SODIUM BENZOATE
FD&C YELLOW NO. 5
CARBOXYPOLYMETHYLENE
SORBITOL
WATER
HYDRATED SILICA
SODIUM LAURYL SULFATE
SACCHARIN SODIUM
FD&C BLUE NO. 1
BENZOIC ACID
GLYCERIN
CETYLPYRIDINIUM CHLORIDE
Product Characteristics
Color green Score
Shape Size
Flavor MINT Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:37000-494-42 119 g in 1 BOTTLE, PUMP None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part355 08/01/2017
Labeler — Procter & Gamble Manufacturing Company (004238200)

Revised: 09/2019 Procter & Gamble Manufacturing Company

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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