Drug Facts

Active Ingredient

Carboxymethylcellulose Sodium 0.5%

Purpose

Eye Lubricant

Use

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 use in the eyes only

Retain outer carton for full product drug facts.

Do not use

If solution changes color or becomes cloudy.

When using this product

Avoid contamination, do not touch tip of container to any surface.
Replace cap after use.

Stop use and ask a doctor if

You experience eye pain, changes in vision, continued redness or irritationn of the eye.
The condition worsens or persists for more than 72 hours.

Keep this and all drugs out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

Shake well before use.
Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Store at room temperature 15°-30°C (59°- 86°F).
Keep tightly closed.

Inactive ingredients

Boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride. Stabilized Oxychloro Complex 2.5%. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or comments?

1-888-767-7913
9am - 5pm EST
Monday - Friday

Distributed by: Cameron Pharmaceuticals, LLC
Louisville, KY 40245

PRINCIPAL DISPLAY PANEL - 2 Bottle Carton

TWIN PACK

CAMERON
PHARMACEUTICALS™

Compare to Refresh Tears® Lubricant
Eye Drops active ingredients† †

NDC 42494-448-05

Lubricant
Eye Drops

CARBOXYMETHYLCELLULOSE SODIUM 0.5%
EYE LUBRICANT

MOISTURIZING

Relieves burning, irritation
& discomfort due to dryness
For mild to moderate dry eye
Sterile

2 Bottles

0.5 OZ (15 mL) Each

1.0 OZ (30 mL) TOTAL

Principal Display Panel - 2 Bottle Carton

CARBOXYMETHYLCELLULOSE SODIUM EYE LUBRICANT
carboxymethylcellulose sodium, unspecified solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:42494-448
Route of Administration	OPHTHALMIC

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:42494-448-05	2 in 1 CARTON	10/18/2024
1		15 mL in 1 BOTTLE, 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	10/18/2024

Labeler - Cameron Pharmaceuticals (078371442)

CARBOXYMETHYLCELLULOSE SODIUM 0.5% EYE LUBRICANT