Label: CLEAR EYES REDNESS RELIEF- naphazoline hydrochloride and glycerin liquid
CLEAR EYES REDNESS RELIEF HANDY POCKET PAL- naphazoline hydrochloride and glycerin liquid

  • NDC Code(s): 67172-796-01, 67172-797-01, 67172-797-06, 67172-797-15
  • 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 September 20, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Clear Eyes Redness Relief

    Drug Facts

  • Active Ingredients

    Glycerin 0.25%

  • Purpose

    Lubricant

  • Active Ingredients

    Naphazoline hydrochloride 0.012%

  • Purpose

    Redness Reliever

  • Uses

    • relieves redness of the eye due to minor eye irritations
    • for the temporary relief of burning and irritation due to dryness of the eye
    • for use as a protectant against further irritation or to relieve dryness of the eye
  • 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 temporarily enlarged

    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 borate

  • Questions?

    1-877-274-1787 Cleareyes.com.

  • SPL UNCLASSIFIED SECTION

    Clear Eyes Redness Relief, Handy Pocket Pal

    Drug Facts

  • Active Ingredients

    Glycerin 0.25%

  • Purpose

    Lubricant

  • Active Ingredients

    Naphazoline hydrochloride 0.012%

  • Purpose

    Redness Reliever

  • Uses

    • relieves redness of the eye due to minor eye irritations
    • for use as a protectant against further irritation or to relieve dryness of the eye for the temporary relief of burning and irritation due to dryness of the eye
  • 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 temporarily enlarged

    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 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 borate

  • Questions?

    1-877-274-1787 cleareyes.com

  • PRINCIPAL DISPLAY PANEL


    CLEAR EYES ®
    REDNESS RELIEF
    LUBRICANT/REDNESS RELIEVER EYE DROPS
    STERILE 0.5 FL OZ (15 mL)

    CLEAR EYES ®
REDNESS RELIEF
LUBRICANT/REDNESS RELIEVER EYE DROPS
STERILE 0.5 FL OZ (15 mL)

  • PRINCIPAL DISPLAY PANEL

    CLEAR EYES ®
    REDNESS RELIEF
    LUBRICANT/REDNESS RELIEVER EYE DROPS
    POCKET PAL®
    STERILE 0.2 FL OZ (6 mL)

    CLEAR EYES ®
REDNESS RELIEF
LUBRICANT/REDNESS RELIEVER EYE DROPS
POCKET PAL®
STERILE 0.2 FL OZ (6 mL)


  • INGREDIENTS AND APPEARANCE
    CLEAR EYES REDNESS RELIEF 
    naphazoline hydrochloride and glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-797
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.12 mg  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67172-797-011 in 1 BOX04/27/2011
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:67172-797-151 in 1 CARTON04/27/2011
    215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    3NDC:67172-797-061 in 1 CARTON04/27/2011
    36 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 finalpart34904/27/2011
    CLEAR EYES REDNESS RELIEF HANDY POCKET PAL 
    naphazoline hydrochloride and glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67172-796
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE.00012 mg  in 1 mL
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN.0025 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67172-796-011 in 1 BOX11/01/2012
    16 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34911/01/2012
    Labeler - Prestige Brands Holdings, Inc. (159655021)