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

Menu
Search

GenTeal

Novartis Pharmaceutical Corporation


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OTC - ACTIVE INGREDIENT SECTION

Mineral oil (15%)
White petrolatum (85%)

OTC - PURPOSE SECTION

Lubricant

INDICATIONS & USAGE SECTION

  • Relieves dryness of the eye.
  • Temporarily relieves discomfort due to minor irritations of the eye or from exposure to wind or sun.
  • As a protectant against further irritation.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

  • if you are sensitive to any ingredient in this product

OTC - WHEN USING SECTION

When using this product do not touch tip of container to any surface. Replace cap after using.

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience any of the following:

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye
  • condition worsens or persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Pull down the lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyelid.

OTHER SAFETY INFORMATION

Store between 15°- 25°C (59°-77°F).

INACTIVE INGREDIENT SECTION

None listed.

OTC - QUESTIONS SECTION

In the U.S. call toll-free 1-866-393-6336; MedInfo@AlconLabs.com
Serious side effects associated with use of this product may be reported to this telephone number.
www.genteal.com

PRINCIPAL DISPLAY PANEL

NDC 0078-0473-97

Night-time PM
Dry Eye Relief

GenTeal ®
LUBRICANT EYE OINTMENT

GenTeal® Night-time PM ointment provides long-lasting relief for night-time comfort.

NIGHT-TIME OINTMENT
Long-lasting Night-time Relief

Alcon®

STERILE 3.5 g (0.12 fl oz)

GenTeal

white petrolatum OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0078-0473
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Mineral Oil 0.15 g
petrolatum 0.85 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 TUBE
2 NDC:0078-0473-97 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2009-12-14


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.