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

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Clear Eyes Complete 7 Sympton Relief

Prestige Brands Holdings, Inc.

Clear Eyes Complete 7 Symptom Relief




FULL PRESCRIBING INFORMATION

Drug Facts

Hypromellose 0.20%

Lubricant

Naphazoline Hydrochloride 0.025%

Redness Reliever

Polysorbate 80 0.50%

Lubricant

Zinc Sulfate 0.25%

Astringent

  • 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.
  • Keep carton for future reference.

boric acid, editate disodium, polyaminoproply biguanide, potassium chloride, sodium chloride, sodium citrate.

1-877-274-1787 Cleareyes.com

Clear
eyes
®
COMPLETE
7 Symptom Relief

ASTRINGENT/LUBRICANT/REDNESS RELIEVER EYE DROPS

Sterile   0.5 FL OZ (15 mL )

Clear Eyes Complete 7 Sympton Relief

Clear Eyes Complete 7 Sympton Relief

Hypromellose, Naphazoline Hydrochloride, Polysorbate 80 and Zinc Sulfate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67172-707
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYPROMELLOSES .5 mg
naphazoline hydrochloride Naphazoline .0625 mg
polysorbate 80 1.25 mg
ZINC SULFATE .625 mg

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
EDETATE DISODIUM
potassium chloride
SODIUM CHLORIDE
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:67172-707-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-06-12


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Be sure to consult your doctor before taking any medication!
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