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

  • NDC Code(s): 67172-999-01, 67172-999-06
  • Packager: Prestige Brands Holdings, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated June 26, 2023

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  • SPL UNCLASSIFIED SECTION

    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 and 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 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 

    • store at 20°-25°C (68°-77°F)
    • remove contact lenses before using
  • Inactive Ingredients

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

  • Questions?

    1-877-274-1787 Cleareyes.com

  • PRINCIPAL DISPLAY PANEL

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

    STERILE 0.5 fl oz (15 mL)

    PRINCIPAL DISPLAY PANEL CLEAR EYES® MAXIMUM ITCHY EYE RELIEF ASTRINGENT LUBRICANT/ REDNESS RELIEVER EYE DROPS STERILE 0.5 fl oz (15 mL)

  • PRINCIPAL DISPLAY PANEL

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

    Handy Pocket Pal

    Sterile 0.2 FL OZ (6 mL)

    Clear eyes® MAXIMUM ITCHY EYE RELIEF ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS Handy Pocket Pal Sterile 0.2 FL OZ (6 mL)

  • INGREDIENTS AND APPEARANCE
    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 HYDROCHLORIDE.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 CARTON09/04/2018
    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 finalpart34903/15/2011
    Labeler - Prestige Brands Holdings, Inc. (159655021)
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