Rembrandt Deeply White Plus Peroxide Whitening description, usages, side effects, indications, overdosage, supplying and lots more!

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Rembrandt Deeply White Plus Peroxide Whitening

Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

Rembrandt Deeply White + Peroxide Whitening Toothpaste Fresh Mint


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Sodium Monofluorophosphate 0.884% w/w (0.0.15% w/v fluoride)

Purpose

Anticavity

Use

aids in the prevention of dental cavities

Warnings

  • Stop use and ask a doctor if oral irritation or tooth sensitivity occurs
  • Keep out of reach of children under 12 years of age.
  • If more than used brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 12 years of age and older:
  • brush teeth thoroughly, preferably after each meal or at least 2 times a day, or as directed by a dentist or physician
  • supervise children as necessary until capable of using without supervision
  • children under 12 years of age: ask a dentist or doctor

Rembrandt Deeply White Plus Peroxide Whitening Other information

  • store at 20° - 25°C (68° – 77° F)

Inactive ingredients

glycerin, hydrated silica, urea peroxide, aluminum hydroxide, modified food starch, flavor, sodium citrate, propylene glycol, cocamidopropyl betaine, papain, sodium lauryl sulfate, carbomer, sodium saccharin, calcium disodium EDTA

Questions or comments?

1-800-548-3663, www.rembrandt.com

Distributed by: Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc., Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 74 g Tube Carton

INTRODUCING
REMBRANDT®
D
DEEPLY WHITE™
+ Peroxide

PEROXIDE TOOTHPASTE FORMULATED FOR SUPERIOR WHITENING

Whitens Deeper* & Restores Enamel
fresh mint

FLUORIDE TOOTHPASTE

NET WT 2.6 oz (74g)

Rembrandt Deeply White Plus Peroxide Whitening

Rembrandt Deeply White Plus Peroxide Whitening

Sodium Monofluorophosphate PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-617
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 1.5 mg

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDRATED SILICA
CARBAMIDE PEROXIDE
aluminum hydroxide
SODIUM CITRATE
propylene glycol
COCAMIDOPROPYL BETAINE
Papain
SODIUM LAURYL SULFATE
SACCHARIN SODIUM DIHYDRATE
EDETATE CALCIUM DISODIUM ANHYDROUS

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 74 in 1 TUBE
2 NDC:42002-617-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-03-16


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