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FAMILY CARE LUBRICANT SINGLE USE EYE

Dosage form: solution/ drops
Ingredients: CARBOXYMETHYLCELLULOSE SODIUM 5mg in 1mL
Labeler: UNITED EXCHANGE CORP
NDC code: 65923-555

Medically reviewed by Drugs.com. Last updated on Aug 21, 2023.

Active ingredient                                                                     Purpose

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

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 of eye
  • if solution changes color or becomes cloudy, do not use


Do not reuse. Once opened, discard

  • Do not touch unit-dose tip of 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.

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° to 86°F (15° to 30°C)
  • 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 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-555
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:65923-555-025 VIAL, SINGLE-USE in 1 CARTON
10.4 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/28/2013
Labeler - UNITED EXCHANGE CORP (840130579)

 
UNITED EXCHANGE CORP

Further information

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