FAMILY CARE LUBRICANT SINGLE USE EYE description, usages, side effects, indications, overdosage, supplying and lots more!

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FAMILY CARE LUBRICANT SINGLE USE EYE

UNITED EXCHANGE CORP

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                                                                     Purpose

Carboxymethylcellulose Sodium 0.5%......................................Eye Lubricant

Purpose

Uses

  • For the temporary relief of burning and discomfort due to dryness of the eye or exposure to wind or sun
  • May be used as a protectant against further irritation

Warnings

For external use only

To avoid contamination, do not touch tip of container to any surface.  Do not reuse. Once opened, discard.

Do not touch unit-dose tip to eye.

If solution changes color or becomes cloudy, do not use.


Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if 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 right away.

Uses

Directions

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

If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor's instructions.

Other information

  • Use only if single use container is intact.
  • Use before expiration date marked on container.
  • Store at 590 to 86oF (150 to 30oC)
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

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

Distributed by:

UNITED EXCHANGE CORP.

17211 Valley View Ave.

Cerritos, CA 90703 USA

MADE IN KOREA

FAMILY CARE LUBRICANT SINGLE USE EYE

FAMILY CARE LUBRICANT SINGLE USE EYE

CARBOXYMETHYLCELLULOSE SODIUM SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65923-555
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
BORIC ACID
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
benzalkonium chloride
SODIUM BORATE
SODIUM CHLORIDE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.8 in 1 VIAL, SINGLE-USE
2 NDC:65923-555-02 5 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-02-28


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Be sure to consult your doctor before taking any medication!
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