LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops

Lubricant Eye Drops by

Drug Labeling and Warnings

Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Oliver Landon Intl Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye Lubricant

Uses    

• ▪ for the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun.
• ▪ protects against further irritation.

Warnings

For external use only

Do not use if solution changes color or becomes cloudy

When using this product

• ▪ do not touch tip of container to any surface to avoid contamination.
• ▪ do not reuse. Once opened, discard.

Stop use and ask a doctor if

• you experience eye pain, changes in vision, continued redness or irritation of the eye
• condition worsens or persists 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

• 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 dryness and discomfort, follow your eye doctor’s instructions.

Other Information   

• ▪ use before expiration date marked on container.
• ▪ store at 59°-86°F (15°-33°C)

RETAIN THIS CARD FOR FUTURE REFERENCE.

Use only if single-use container is intact.

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.

Questions or Comments?

1 (800) 839-5929

PRINCIPAL DISPLAY PANEL

Lubricant Eye Drops
0.4 ml (0.014 fl oz) per vial

INGREDIENTS AND APPEARANCE

LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59276-905
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg  in 1 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)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59276-905-05	5 in 1 CELLO PACK	02/25/2019
1		0.4 mL in 1 VIAL, SINGLE-USE; 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	02/25/2019

Labeler - Oliver Landon Intl Inc. (815240195)