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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Clear Eyes Cooling Itchy Eye Relief

Drug Facts

Active ingredients

Glycerin 0.25%

Purpose

Lubricant

Active ingredients

Naphazoline hydrochloride 0.012%

Purpose

Redness Reliever

Active ingredients

Zinc sulfate 0.25%

Purpose

Astringent

Uses

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 of container 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 or persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

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

Other information

Inactive ingredients

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

Questions?

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

PRINCIPAL DISPLAY PANEL

NEW Clear eyes® 
COOLING COMFORT
Astringent/Lubricant/Redness Relief Eye Drops
ITCHY EYE RELIEF
Cools Eye Irritations
Relieves Itching &Burning
STERILE 0.5 FL OZ (15 ML)

PRINCIPAL DISPLAY PANEL
NEW Clear eyes® 
COOLING COMFORT
ITCHY EYE RELIEF
STERILE 0.5 FL OZ (15 ML)

CLEAR EYES COOLING ITCHY EYE RELIEF 
naphazoline hydrochloride and glycerin and zinc sulfate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-292
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE.12 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 mg  in 1 mL
ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC SULFATE2.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
MENTHOL (UNII: L7T10EIP3A)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
BETADEX (UNII: JV039JZZ3A)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-292-011 in 1 BOX02/15/2011
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34902/15/2011
Labeler - Prestige Brands Holdings, Inc. (159655021)
Establishment
NameAddressID/FEIBusiness Operations
Aspen SVP Pty Ltd569162139MANUFACTURE(67172-292)

Revised: 9/2017
Document Id: 592ab4e9-160a-4e86-96e5-9900e1ff23d7
Set id: a710be3f-fa5b-46a6-87b5-5a4d1f807e1c
Version: 5
Effective Time: 20170928
 
Prestige Brands Holdings, Inc.