Glister Multi-Action Fluoride Toothpaste description, usages, side effects, indications, overdosage, supplying and lots more!

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Glister Multi-Action Fluoride Toothpaste

Access Business Group, LLC

Glister Multi-action Fluoride Toothpaste


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Sodium fluoride 0.21%

Purpose

Anticavity

Glister Multi-Action Fluoride Toothpaste Uses

Aids in the prevention of dental cavities

Warning

If more than used for brushing is accidentally swallowed, get medical help or contact  a Poison Control Center right away.

Keep out of reach of children

under 6 years of age

Directions

  • Do not swallow
  • Adults and children 2 years and over: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or doctor
  • Instruct children under 6 years in good rinsing habits (to reduce swallowing)
  • Supervise children as necessary until capable of using without supervision
  • Children under 2 years, ask a dentist or doctor.

Inactive Ingredients

Sorbitol, Water, Hydrated Silica, Glycerin, Propylene Glycol, Sodium Lauryl Sulfate, Xylitol, Cellulose Gum, PEG-8, Flavor, Titanium Dioxide, Xanthan Gum, Sodium Saccharin, Methylparaben, Propylparaben, FDandC Blue No. 1

With regular brushing, glister multi-action fluoride toothpaste helps remove plaque. This product contains SYLODENT polishing agent which safely cleans and helps eliminate stains to whiten teeth. To enhance your overall oral health, use the complete glister oral care system

Trademark is used by Access under license.

Dist. by Access Business Group International LLC, Ada, MI 49355

Glister multi-action fluoride toothpaste

Multiple action

whitens teeth

removes plaque

fights cavities

safely cleans

freshens breath

promotes remineralization

MADE IN U.S.A.


Glister Multi-Action Fluoride Toothpaste

Glister Multi-Action Fluoride Toothpaste

Glister Multi-Action Fluoride Toothpaste

SODIUM FLUORIDE PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10056-530
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.21 g

Inactive Ingredients

Ingredient Name Strength
sorbitol
water
HYDRATED SILICA
GLYCERIN
propylene glycol
SODIUM LAURYL SULFATE
Xylitol
CARBOXYMETHYLCELLULOSE SODIUM
polyethylene glycol
titanium dioxide
XANTHAN GUM
saccharin sodium
METHYLPARABEN
PROPYLPARABEN
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 65 in 1 TUBE
2 191 in 1 TUBE
3 NDC:10056-530-06 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2011-04-11


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