Clear Eyes Complete 7 Symptom Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Clear Eyes Complete 7 Symptom Relief

Prestige Brands Holdings, Inc.

Clear Eyes Complete




FULL PRESCRIBING INFORMATION

Drug Facts

Hypromellose 0.20%

Lubricant

Naphazoline Hydrochloride 0.025%

Redness Reliever

Polysorbate 80 0.50%

Lubricant

Zinc Sulfate 0.25%

Lubricant

  • 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.

For external use only.

if solution changes color or becomes cloudy.

if you have narrow angle glaucoma

  • 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.
  • 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

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

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

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

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

1-877-274-1787

www.cleareyes.com

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

Sterile   0.5 FL OZ (15 mL )

Clear Eyes Complete 7 Symptom Relief

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 .625 mL
polysorbate 80 1.25 mL
naphazoline hydrochloride Naphazoline .0625 mL
hypromellose .5 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 15 in 1 BOTTLE, DROPPER
2 NDC:67172-595-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-03-01


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Be sure to consult your doctor before taking any medication!
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