Clear Eyes Triple Action description, usages, side effects, indications, overdosage, supplying and lots more!

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Clear Eyes Triple Action

Prestige Brands Holdings, Inc.

Clear Eyes Triple Action




FULL PRESCRIBING INFORMATION

Drug Facts

Polyvinyl alcohol 0.5%

Povidone 0.6%

Lubricant

Tetrahydrozoline hydrochloride 0.05%

Redness Reliever

  • For the temporary relief of burning & irritation due to dryness of the eye.
  • For use as a protectant against further irritation or to relieve dryness of the eye.
  • Relieves redness of the eye due to minor eye irritations.

For external use only.

solution changes color or becomes cloudy.

narrow angle glaucoma.

  • 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 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.

benzalkonium chloride, dextrose, dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate

UP TO 8 HOURS OF SOOTHING COMFORT
Clear eyes®
TRIPLE ACTION RELIEF
LUBRICANT/REDNESS RELIEVER EYE DROPS
● Relieves Redness
● Soothes & Moisturizes
● Calms Irritation
● Fast Acting
Sterile 0.5 FL OZ (15 mL)

Clear Eyes Triple Action

Clear Eyes Triple Action

Polyvinyl Alcohol and Povidone and Tetrahydrozoline Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67172-898
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POLYVINYL ALCOHOL .00125 mL
povidone .0015 mL
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE .000125 mL

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
DEXTROSE
SODIUM PHOSPHATE, DIBASIC
EDETATE DISODIUM
sodium phosphate, monobasic
potassium chloride
water
SODIUM BICARBONATE
SODIUM CHLORIDE
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:67172-898-01 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-03-15


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Be sure to consult your doctor before taking any medication!
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