Label: CLEAR EYES COMPLETE 7 SYMPTOM RELIEF- zinc sulfate, polysorbate 80, naphazoline hydrochloride and hypromellose liquid 

  • Label RSS
  • NDC Code(s): 67172-595-01
  • Packager: Prestige Brands Holdings, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 08/10

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

    Close
  • Active Ingredients

    Hypromellose 0.20%

    Close
  • Purpose

    Lubricant

    Close
  • Active Ingredients

    Naphazoline Hydrochloride 0.025%

    Close
  • Purpose

    Redness Reliever

    Close
  • Active Ingredients

    Polysorbate 80 0.50%

    Close
  • Purpose

    Lubricant

    Close
  • Active Ingredients

    Zinc Sulfate 0.25%

    Close
  • Purpose

    Lubricant

    Close
  • 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 the dryness of the eye.
    • Relieves redness of the eye due to minor eye irritations.
    Close
  • 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 of this product 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
    • symptoms last for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

    Close
  • Directions

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

    Close
  • Other Information

    • Store at room temperature.
    • Remove contact lenses before using.
    • Tamper Evident: Do not use if neckband on bottle is broken or missing.
    Close
  • Inactive Ingredients

    calcium chloride, citric acid, edetate disodium, magnesium chloride, potassium chloride, purified water, sodium citrate, sodium chloride and sorbic acid.

    Close
  • Questions?

    1-877-274-1787

    www.cleareyes.com

    Close
  • PRINCIPAL DISPLAY PANEL

    Clear
    eyes
    ®
    COMPLETE
    ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS

    Sterile 0.5 FL OZ (15 mL)

    PRINCIPAL DISPLAY PANEL
Clear Eyes Complete
0.5 FL OZ (15 mL)

    Close
  • INGREDIENTS AND APPEARANCE
    CLEAR EYES COMPLETE 7 SYMPTOM RELIEF 
    hypromellose and naphazoline hydrochloride and polysorbate 80 and zinc sulfate liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:67172-595
    Route of Administration OPHTHALMIC DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ZINC SULFATE (ZINC) ZINC SULFATE .625 mL  in 1 mL
    POLYSORBATE 80 (POLYSORBATE 80) POLYSORBATE 80 1.25 mL  in 1 mL
    NAPHAZOLINE HYDROCHLORIDE (NAPHAZOLINE) NAPHAZOLINE HYDROCHLORIDE .0625 mL  in 1 mL
    HYPROMELLOSE (HYPROMELLOSE) HYPROMELLOSE .5 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    CALCIUM CHLORIDE  
    CITRIC ACID  
    EDETATE DISODIUM  
    MAGNESIUM CHLORIDE  
    POTASSIUM CHLORIDE  
    WATER  
    SODIUM CITRATE  
    SODIUM CHLORIDE  
    SORBIC ACID  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:67172-595-01 1 in 1 BOX
    1 15 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part349 03/01/2010
    Labeler - Prestige Brands Holdings, Inc. (159655021)
    Establishment
    Name Address ID/FEI Business Operations
    Altaire Pharmaceuticals Inc. 786790378 MANUFACTURE
    Close