Listerine Whitening Fluoride Anticavity description, usages, side effects, indications, overdosage, supplying and lots more!

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Listerine Whitening Fluoride Anticavity

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

Listerine Whitening Fluoride Anticavity Toothpaste Original Gel


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Sodium Monofluorophosphate 0.76% (0.13% w/v fluoride ion)

Purpose

Anticavity

Use

aids in the prevention of dental cavities

Warnings

Keep out of reach of children under 6 years 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 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
  • children 2-6 years use only a pea size amount
  • Instruct children under 12 years of age in good brushing and rinsing habits (to minimize swallowing)
  • supervise children as necessary until capable of using without supervision
  • children under 2 years of age: ask a dentist or doctor

Listerine Whitening Fluoride Anticavity Other information

  • store at (59° - 77°F)

Inactive ingredients

sorbitol solution, water, hydrated silica, glycerin, PEG-32, sodium lauryl sulfate, cellulose gum, sodium saccharin, eucalyptol, methyl salicylate, thymol, phosphoric acid, menthol, zinc citrate, sodium phosphate, xanthan gum, benzoic acid, flavors, FD&C blue no. 1, D&C yellow no. 10

Questions?

Call toll-free 888-222-0182 or 215-273-8755 (collect)

PRINCIPAL DISPLAY PANEL - 119g Tube Carton

NEW

FOR A HEALTHY LOOKING WHITE SMILE

LISTERINE®
WHITENING®

fluoride anticavity toothpaste
original gel

VIBRANT WHITE® MINT

Whitens by removing
surface stains®

NET WT. 4.2 OZ. (119g)

Listerine Whitening Fluoride Anticavity

Listerine Whitening Fluoride Anticavity

Sodium Monofluorophosphate GEL, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-428
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 7.6 mg

Inactive Ingredients

Ingredient Name Strength
sorbitol
water
HYDRATED SILICA
GLYCERIN
POLYETHYLENE GLYCOL 1500
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
saccharin sodium
EUCALYPTOL
methyl salicylate
THYMOL
phosphoric acid
MENTHOL
Zinc Citrate
sodium phosphate
XANTHAN GUM
BENZOIC ACID
FD&C BLUE NO. 1
D&C YELLOW NO. 10

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 119 in 1 TUBE
2 NDC:42002-428-09 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-11-12


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