FAMILY CARE LUBRICANT SINGLE USE EYE- carboxymethylcellulose sodium solution/ drops 
UNITED EXCHANGE CORP

----------

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

image description

FAMILY CARE LUBRICANT SINGLE USE EYE 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-555
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65923-555-025 in 1 CARTON03/28/2013
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01802/28/201312/30/2022
Labeler - UNITED EXCHANGE CORP (840130579)

Revised: 1/2025
 
UNITED EXCHANGE CORP