CLEAR EYES MAXIMUM ITCHY EYE RELIEF - glycerin, naphazoline hydrochloride and zinc sulfate liquid 
Prestige Brands Holdings, Inc.

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Clear Eyes Maximum Itchy Eye Relief

Drug Facts

Active Ingredient

Glycerin 0.25%

Purpose

Lubricant

Active Ingredient

Naphazoline hydrochloride 0.012%

Purpose

Redness Reliever

Active Ingredient

Zinc Sulfate 0.25%

Purpose

Astringent

Uses

• For use as a protectant against further irritation or to relieve dryness of the eye.
  
• For the temporary relief of burning & irritation due to dryness of the eye.
  
• Relieves redness of the eye due to minor eye irritations.

Warnings

For external use only.

Do not use if

solution changes color or becomes cloudy.

Ask a doctor before use if you have

narrow angle glaucoma.

When using this product

• To avoid contamination, do not touch tip to any surface.
  
• Replace cap after using.
  
• Overuse may produce increased redness of the eye.
  
• Pupils may become enlarged temporarily.

Stop use & ask a doctor if

• you experience eye pain
  
• you experience changes in vision
  
• you experience continued redness or irritation of the eye
  
• the condition worsens
  
• symptoms last 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

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Other Information

• Store at room temperature.
  
• Remove contact lenses before using.
  
• Tamper Evident. Do not use if neckband on bottle is broken or missing.

Inactive Ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium chloride, sodium citrate

Questions?

1-877-274-1787 www.cleareyes.com

PRINCIPAL DISPLAY PANEL

UP TO 8 HOURS OF SOOTHING COMFORT
Clear eyes®
MAXIMUM ITCHY EYE RELIEF
ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS
● Relieves Itching, Burning, Watery & Red Eyes
● Soothes & Moisturizes
● Fast Acting
Sterile 0.5 FL OZ (15 mL)

CLEAR EYES MAXIMUM ITCHY EYE RELIEF  glycerin and naphazoline hydrochloride and zinc sulfate   liquid

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 67172-999 Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (GLYCERIN) GLYCERIN 0.625 mL  in 1 mL NAPHAZOLINE HYDROCHLORIDE (NAPHAZOLINE) NAPHAZOLINE HYDROCHLORIDE 0.21 mL  in 1 mL ZINC SULFATE (ZINC) ZINC SULFATE 0.625 mL  in 1 mL

Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE   BORIC ACID   EDETATE DISODIUM   WATER   SODIUM CHLORIDE   SODIUM CITRATE

Product Characteristics Color WHITE Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 67172-999-01 1 BOTTLE In 1 BOX contains a BOTTLE, DROPPER 1 15 mL In 1 BOTTLE, DROPPER This package is contained within the BOX (67172-999-01)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part349	03/15/2011

Labeler - Prestige Brands Holdings, Inc. (159655021)

Establishment
Name	Address	ID/FEI	Operations
Aspen SVP (Pty) Ltd.		538473091	MANUFACTURE

Revised: 03/2011Prestige Brands Holdings, Inc.