LUBRICANT EYE- carboxymethylcellulose sodium solution/ drops

Lubricant Eye by

Drug Labeling and Warnings

Lubricant Eye by is a Otc medication manufactured, distributed, or labeled by The Kroger Co., Unimed Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Carboxymethylcellulose sodium 0.5%

PURPOSE

Purpose
Carboxymethylcellulose sodium.............Eye Lubricant

INDICATIONS & USAGE

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

​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.

DOSAGE & ADMINISTRATION

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 SAFETY INFORMATION

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 INGREDIENT

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

Questions or comments?
1-800-632-6900

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30142-373
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROCHLORIC ACID (UNII: QTT17582CB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30142-373-33	30 in 1 BOX	06/01/2015
1		0.5 mL in 1 VIAL, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	06/01/2015

Labeler - The Kroger Co. (006999528)

Registrant - Unimed Pharmaceuticals, Inc. (689852052)

Establishment
Name	Address	ID/FEI	Business Operations
Unimed Pharmaceuticals, Inc.		689852052	label(30142-373) , manufacture(30142-373) , pack(30142-373)