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Colgate

Colgate-Palmolive Company

Colgate Total Whitening Gel


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Sodium fluoride 0.24% (0.14% w/v fluoride ion) Anticavity
Triclosan 0.30% Antigingivitis

Colgate Uses

aids in the prevention of:

  • cavities
  • plaque
  • gingivitis

Warnings

Keep out of the 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.

Ask a dentist before use if you have

  • bleeding or redness lasting more than 2 weeks
  • pain, swelling, pus, loose teeth, or more spacing between teeth

These may be signs of periodontitis, a serious form of gum disease.

Directions

supervise children as necessary until capable of using without supervision.

adults and children 6 years of
age and older
brush teeth thoroughly, preferably after each meal or at least
twice a day, or as directed by a dentist or a physician
children under 12 years instruct in good brushing and rinsing habits
(to minimize swallowing)
children under 6 years do not use unless directed by a dentist or a physician

Antiplaque and antigingivitis use not proven in children.

Inactive ingredients

water, hydrated silica, glycerin, sorbitol, PVM/MA copolymer, sodium lauryl sulfate, cellulose gum, flavor, sodium hydroxide, propylene glycol, carrageenan, sodium saccharin, mica, titanium dioxide, FD&C blue no.1

Questions or comments?

Call toll-free 1-800-468-6502

Dist. by:
COLGATE-PALMOLIVE COMPANY
New York, NY 10022

www.colgatetotal.com

PRINCIPAL DISPLAY PANEL - 170 g Tube Carton

NEW
STAND-UP
CAP

Helps Prevent: Cavities • Gingivitis • Plaque
Fights Tartar • Freshens Breath • Whitens

Colgate®
Anticavity Fluoride and Antigingivitis Toothpaste

Total ®
Whitening
Gel

ADA
Accepted
American
Dental
Association ®

NET WT 6.0 OZ (170 g)

Colgate

Colgate

Silicon Dioxide, Sodium Fluoride, and Triclosan GEL, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:35000-002
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SILICON DIOXIDE 50 mg
SODIUM FLUORIDE FLUORIDE ION 2.4 mg
TRICLOSAN TRICLOSAN 3 mg

Inactive Ingredients

Ingredient Name Strength
water
HYDRATED SILICA
GLYCERIN
sorbitol
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
SODIUM HYDROXIDE
propylene glycol
CARRAGEENAN
saccharin sodium
MICA
titanium dioxide
FD&C BLUE NO. 1

Product Characteristics

Color
WHITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 204 in 1 TUBE
2 170 in 1 TUBE
3 221 in 1 TUBE
4 NDC:35000-002-78 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020231 2010-09-20


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Be sure to consult your doctor before taking any medication!
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