PureLife APF description, usages, side effects, indications, overdosage, supplying and lots more!

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PureLife APF

PureLife Dental


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Fluoride Ion 1.23%.

Available from 2.09% Sodium Fluoride and Hydrofluoric Acid.

Purpose

Anticaries Treatment

PureLife APF Indications and Usage

  • A stable thixotropic fluoride treatment gel used to help prevent dental decay.
  • For Professional Office Use Only. This product is not intended for home or unsupervised consumer use.

Warnings

  • Keep out of reach of children.
  • Do not swallow. If product is accidentally swallowed in quantities greater than would normally occur with a treatment gel, seek medical help or contact a Poison Control Center right away.
  • Read directions carefully before using.

Dosage and Administration

Shake well before use. This is a one minute or four minute fluoride gel for in-office patient use. It is normally used as a preventative caries treatment two times a year.

1. After thorough prophylaxis, fill two single or one dual try, one third full with gel. Air dry teeth and insert trays into the mouth.

2. Instruct patient to bite down lightly but firmly for one minute (80% effectiveness) or four minutes (100% effectiveness).

3. Remove trays. Instruct patient to expectorate any excess gel and not to eat or drink for at least 30 minutes.

Other Information

Store at controlled temperature 59°-86°F (15°-30°C).

Protect from freezing.

Inactive Ingredients

Citric Acid, FD&C Red #40, Flavor, Magnesium Aluminum Silicate, Phosphoric Acid, Polysorbate 20, Sodium Benzoate, Sodium Saccharin, Titanium Dioxide, Water, Xanthan Gum, Xylitol.

PureLife APF

PureLife APF

Sodium Fluoride GEL

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:68987-014
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 5.6 g

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
FD&C RED NO. 40
titanium dioxide
magnesium aluminum silicate
phosphoric acid
POLYSORBATE 20
SODIUM BENZOATE
saccharin sodium
water
XANTHAN GUM
Xylitol

Product Characteristics

Color
pink

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68987-014-15 454 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-12-18


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