Target Lubricant Eye Drops Preservative Free 70 ct (PLD)

Active ingredient
Carboxymethylcellulose sodium 0.5%

Purpose
Carboxymethylcellulose sodium.............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

do not reuse
once opened, discard
to avoid contamination do not touch tip of container to any surface
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 (1-800-222-1222) 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°-25°C (59°-77°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.

box

LUBRICANT EYE DROPS PRESERVATIVE FREE
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-150
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11673-150-01	70 in 1 BOX	02/12/2019
1		0.4 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	02/12/2019

Labeler - Target Corporation (006961700)

Registrant - Unimed (689852052)

Name	Address	ID/FEI	Business Operations
Establishment
KC Pharmaceuticals, Inc.		174450460	pack(11673-150) , label(11673-150)

Name	Address	ID/FEI	Business Operations
Establishment
Unimed		689852052	manufacture(11673-150)