Retaine CMC Lubricant Eye Drops description, usages, side effects, indications, overdosage, supplying and lots more!

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Retaine CMC Lubricant Eye Drops

OCuSOFT INC.
OCuSOFT INC.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Carboxymethylcellulose sodium 0.5%................................. Eye Lubricant

Retaine CMC Lubricant Eye Drops Uses

  • Relieves dryness of the eye.
  • Temporarily relieves discomfort due to minor irritations of the eye or from exposure to wind or sun.
  • As a protectant against further irritation. 

Warnings

For use in the eyes only.
Do not use if solution changes color or becomes cloudy.

When using this product

  • do not touch tip of container to any surface to avoid contamination.
  • do not reuse once opened.

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness or irritation of the eye.
  • the condition worsens or persists for more than 72 hours.

KEEP OUT OF THE REACH OF CHILDREN

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

Directions

  • To open, TWIST AND PULL TAB TO REMOVE.
  • Instill 1 or 2 drops into affected eye(s) as needed and discard container.

Other Information

  • Use only if printed tamper seals on top and bottom flaps are intact.
  • Use only if twist top of single-dose container is intact.
  • Store between 15º-30ºC (59º-86ºF).

Inactive Ingredients

Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium lactate.  May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.


Questions or comments?

Call (800) 233-5469 M-F 8:30AM-5:00PM CST or visit www.retainebrand.com

Purpose

Eye Lubricant

Retaine CMC Lubricant Eye Drops

Retaine CMC Lubricant Eye Drops

Carboxymethylcellulose Sodium SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54799-897
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 5 mg

Inactive Ingredients

Ingredient Name Strength
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
SODIUM CHLORIDE
sodium lactate
water
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.4 in 1 VIAL, SINGLE-DOSE
2 NDC:54799-897-30 30 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-09-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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