Kroger Lubricant Eye Drops (PLD)

Active ingredient
Carboxymethylcellulose sodium 0.5%

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

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

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.

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

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 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 or comments?
1-800-632-6900

Carton

KROGER LUBRICANT EYE
carboxymethylcellulose sodium solution/ drops

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	06/01/2015

Labeler - The Kroger Co. (006999528)

Registrant - Unimed Pharmaceuticals, Inc. (689852052)

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