GENTEAL MILD TO MODERATE - hypromellose 2910 (4000 mpa.s) liquid 
Novartis Pharmaceuticals Corporation

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Drug Facts

Active ingredient

hypromellose (0.3%)

Purpose

Lubricant

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 irritation.

Warnings

Do not use if solution changes color or becomes cloudy.

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

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 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.

Other Information

Store between 15⁰-30⁰C (59⁰-86⁰F).

Questions? call toll-free 1-866-393-6336, weekdays, 8:30 AM - 5:00 PM EST.

Serious side effects associated with use of this product may be reported to this number.

Inactive ingredients

boric acid, GenAqua (sodium perborate), phosphonic acid, potassium chloride, purified water, and sodium chloride

PRINCIPAL DISPLAY PANEL

PRODUCT PACKAGING

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

GenTeal

Mild to Moderate

Dry Eye Relief

Lubricant Eye Drops

Liquid Drops

Fast, Soothing Relief

Preservative Free in the Eye

USE ONLY IF TAMPER EVIDENT SEAL MARKED NOVARTIS IS INTACT.

GENTEAL  MILD TO MODERATE hypromellose   liquid

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0078-0518 Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPROMELLOSE 2910 (4000 MPA.S) (HYPROMELLOSE 2910 (4000 MPA.S)) HYPROMELLOSE 2910 (4000 MPA.S) 0.003 L  in 1 L

Inactive Ingredients Ingredient Name Strength PHOSPHORIC ACID   BORIC ACID   POTASSIUM CHLORIDE   SODIUM CHLORIDE   SODIUM PERBORATE   WATER

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0078-0518-24 0.015 L In 1 BOTTLE, DROPPER None 2 0078-0518-16 0.025 L In 1 BOTTLE, DROPPER None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	09/14/2009

Labeler - Novartis Pharmaceuticals Corporation (002147023)

Revised: 12/2010Novartis Pharmaceuticals Corporation