CLEAR EYES MAXIMUM ITCHY EYE RELIEF- glycerin and 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

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
  • overuse may produce increased redness of the eye

Stop useandask 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 symptoms last 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, edetate disodium, purified water, sodium chloride, sodium citrate

Questions?

1-877-274-1787Cleareyes.com

PRINCIPAL DISPLAY PANEL

CLEAR
EYES ®
MAXIMUM
ITCHY EYE

RELIEF
ASTRINGENT LUBRICANT/
REDNESS RELIEVER EYE DROPS

PRINCIPAL DISPLAY PANEL CLEAR EYES® MAXIMUM ITCHY EYE RELIEF ASTRINGENT LUBRICANT/ REDNESS RELIEVER EYE DROPS

PRINCIPAL DISPLAY PANEL

Clear eyes®
MAXIMUM
ITCHY EYE RELIEF
ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS

PRINCIPAL DISPLAY PANEL Clear eyes® MAXIMUM ITCHY EYE RELIEF ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS

CLEAR EYES MAXIMUM ITCHY EYE RELIEF 
glycerin and naphazoline hydrochloride and zinc sulfate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-999
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 mg  in 1 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.12 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)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67172-999-011 in 1 BOX03/15/2011
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:67172-999-061 in 1 CARTON09/04/201805/31/2020
26 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 DrugM01803/15/2011
Labeler - Prestige Brands Holdings, Inc. (159655021)

Revised: 9/2026
Document Id: 5b2756d6-2d54-22a4-e063-6394a90aed7d
Set id: 326a1462-78d1-42d6-8257-7e4f00d1f215
Version: 13
Effective Time: 20260910
 
Prestige Brands Holdings, Inc.