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Leader Lubricant Eye by Cardinal Health

Medically reviewed on February 19, 2018

Dosage form: solution/ drops
Ingredients: CARBOXYMETHYLCELLULOSE SODIUM 5mg in 1mL
Labeler: Cardinal Health
NDC Code: 49781-032

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient                                            Purpose

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

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.

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 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49781-032
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE 
MAGNESIUM CHLORIDE 
POTASSIUM CHLORIDE 
WATER 
SODIUM CHLORIDE 
SODIUM LACTATE 
HYDROCHLORIC ACID 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:49781-032-301 VIAL, SINGLE-USE in 1 BOX
1.04 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/18/2014
Labeler - Cardinal Health (097537435)

 
Cardinal Health

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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