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

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GenTeal

Novartis Pharmaceuticals Corporation

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Hypromellose (0.3%)

Purpose

Lubricant

GenTeal Uses

  • 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 irritations.

Warnings

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

Do not use if gel changes color or becomes cloudy.

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

Keep out of reach of children. 

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

Directions

Put 1 or 2 drops in the affected eye(s) as needed.

GenTeal Other information

Store between 15⁰- 30⁰C (59⁰-86⁰F).

Inactive ingredients

carbopol 980, GenAqua (sodium perborate), phosphonic acid, purified water, sodium hydroxide, and sorbitol.

Questions?

call toll-free 1-866-393-6336, weekdays, 8:30 AM - 5:00 PM EST.  Serious side effects associated with the use of this product may be reported to this number.

PRINCIPAL DISPLAY PANEL

PACKAGE LABELING

The product packaging shown below represents a sample of that currently in
use. Additional packaging may also be available.

GenTeal

Severe Dry Eye Relief

Lubricant Eye Gel

GEL

Long-lasting, Powerful Relief

Preservative Free in the Eye

USE ONLY IF TAMPER EVIDENT SEAL MARKED NOVARTIS IS INTACT.


GenTeal

GenTeal

HYPROMELLOSE GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0078-0429
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYPROMELLOSE 2910 (4000 MPA.S) .003 g

Inactive Ingredients

Ingredient Name Strength
SODIUM PERBORATE
phosphoric acid
water
SODIUM HYDROXIDE
sorbitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 TUBE
2 10 in 1 TUBE
3 NDC:0078-0429-47 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2009-09-14


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Be sure to consult your doctor before taking any medication!
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