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Lubricant Eye by The Kroger Co.

Medically reviewed on April 12, 2018

Dosage form: solution/ drops
Ingredients: CARBOXYMETHYLCELLULOSE SODIUM 0.5g in 100mL
Labeler: The Kroger Co.
NDC Code: 30142-373

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
Carboxymethylcellulose sodium 0.5%

Purpose
Carboxymethylcellulose sodium.............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

​Warnings

For external use only.

Do not use if solution changes color or becomes cloudy.

When using the product 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.

Stop use and ask a doctor if

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

Keep out of reach of children. If accidentally 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 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

  • Store at 15°-30°C (59°-86°F).
  • Use only if single-use container is intact.
  • Use before expiration date marked on container.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE

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

Questions or comments?
1-800-632-6900

LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-373
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE 
MAGNESIUM CHLORIDE 
POTASSIUM CHLORIDE 
WATER 
SODIUM CHLORIDE 
SODIUM LACTATE 
SODIUM HYDROXIDE 
HYDROCHLORIC ACID 
Packaging
#Item CodePackage Description
1NDC:30142-373-3330 VIAL, DISPENSING in 1 BOX
10.5 mL in 1 VIAL, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34906/01/2015
Labeler - The Kroger Co. (006999528)
Registrant - Unimed Pharmaceuticals, Inc. (689852052)
Establishment
NameAddressID/FEIOperations
Unimed Pharmaceuticals, Inc.689852052label(30142-373), manufacture(30142-373), pack(30142-373)

 
The Kroger Co.

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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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