Family Care Single-Use Eye

Manufacturer
United Exchange Corp.
Effective date
2017-08-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:12:24

Label at a glance#

ProductFamily Care Single-Use Eye
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure10 sections

Storage and handling

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.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                             Purpose

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

OTC - PURPOSE SECTION

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 SECTION

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 to eye.
  • If solution changes color or becomes cloudy, do not use.

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

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.

STORAGE AND HANDLING SECTION

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.

INACTIVE INGREDIENT SECTION

Inactive ingredients 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.

DOSAGE & ADMINISTRATION SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65923-58365923-583-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d104be17-924a-8bc5-e053-2995a90a8ffaaad3a896-adfd-4dc7-bbe8-7a37e89e695d2021-11-17WarningsExact identifier
spl set id: aad3a896-adfd-4dc7-bbe8-7a37e89e695d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.