Leader Lubricant Eye description, usages, side effects, indications, overdosage, supplying and lots more!

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Leader Lubricant Eye

Cardinal Health




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                                            Purpose

Carboxymethylcellulose sodium 0.5%............. Eye lubricant

Purpose

Uses

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

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 thatn 72 hours.

Keep out of reach of children. If swallowed get medical help or contact a Poision 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 59°-86°F (15°-30°C)
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

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

DISTRIBUTED BY:

CARDINAL HEALTH

DUBLIN, OHIO 43017

Leader Lubricant Eye

Leader Lubricant Eye

Carboxymethylcellulose Sodium SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49781-032
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
water
SODIUM CHLORIDE
sodium lactate
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 .04 in 1 VIAL, SINGLE-USE
2 NDC:49781-032-30 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2014-02-18


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Be sure to consult your doctor before taking any medication!
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