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

Drug Label Information

Updated October 25, 2024

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  • 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 DrugM01804/27/2011
    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 DrugM01811/01/2012
    Labeler - Prestige Brands Holdings, Inc. (159655021)
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