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Family Care Artificial Eye

Medically reviewed by Drugs.com. Last updated on Apr 13, 2020.

Dosage form: solution/ drops
Ingredients: POLYVINYL ALCOHOL, UNSPECIFIED .05mg in 1mL, POVIDONES .06mg in 1mL
Labeler: United Exchange Corp.
NDC Code: 65923-512

Further information

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

Active ingredients                                            Purpose

Polyvinyl alcohol 0.5%....................................Lubricant

Povidone 0.6%..............................................Lubricant

Uses

  • For the temporary relief of burning & irritation due to dryness of the eye
  • For use as a protectant against further irritation or to relieve dryness of the eye

Warnings

For external use only.

Do not use

  • if solution changes color or becomes cloudy.

When using this product

  • to avoid contamination, do not touch tip to any surface
  • replace cap after using

Stop use and ask a doctor if

  • you experience eye pain
  • you experience changes in vision
  • you experience continued redness or irritation of the eye
  • the condition worsens
  • symptoms last for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

  • store at room temperature
  • remove contact lenses before using

Inactive ingredients

benzalkonium chloride, dibasic sodium phosphate hydrate, edetate disodium, glucose, hydrochloric acid, monobasic sodium phosphate, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate hydrate, sodium hydroxide

Distributed by:

United Exchange Corp.

17211 Valley  View Ave.

Cerritos, CA 90703 U.S.A.

www.ueccorp.com

Toll Free: 1 800 814 8028

Made in Korea

FAMILY CARE ARTIFICIAL EYE 
polyvinyl alcohol, and povidones solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65923-512
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYVINYL ALCOHOL, UNSPECIFIED (POLYVINYL ALCOHOL, UNSPECIFIED) POLYVINYL ALCOHOL, UNSPECIFIED.05 mg  in 1 mL
POVIDONES (POVIDONE) POVIDONES.06 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
SODIUM PHOSPHATE, DIBASIC DIHYDRATE 
EDETATE DISODIUM 
HYDROCHLORIC ACID 
SODIUM PHOSPHATE, MONOBASIC 
POTASSIUM CHLORIDE 
WATER 
SODIUM BICARBONATE 
SODIUM CHLORIDE 
SODIUM CITRATE 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:65923-512-151 BOTTLE, DROPPER in 1 BOX
115 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34904/22/2016
Labeler - United Exchange Corp. (840130579)

 
United Exchange Corp.