LUBRICANT DROPS- carboxymethylcellulose sodium solution/ drops 
CARDINAL HEALTH 110, LLC. DBA LEADER

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Sterile Lubricant Eye Drops

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.
For use as a protectant against further irritation or to relieve dryness of the eye.

Warnings

For external use only.
To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
If solution changes color or becomes cloudy, do not use.

Stop use and ask a doctor if

you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the 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

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
Use before expiration date marked on container.
Discard 90 days after opening
Store at 59°-86°F (15°-30°C).
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; stabilized oxychloro complex; and sodium chloride. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

.

TAMPER EVIDENT

Do not use if tape seals on carton top and bottom flaps are damaged or missing.

*This product is not manufactured or distributed by Allergan, Inc., owner of the registered trademark

Refresh Tears® Lubricant Eye Drops.

DISTRIBUTED BY CARDINAL HEALT

DUBLIN, OHIO 43017

www.myleader.com 1-800-200-6313

Made in India

100% Money Back Guarantee

Return to place of purchase if not satisfied.

Code: MH/DRUGS/28-KD/283

CIN 5698378

REV. 2/21

CIN 5698386

REV. 2/21

Principal Display Panel

LEADER®

NDC 70000-0090-1

Sterile

Lubricant

Eye Drops

Carboxymethylcellulose

Sodium, 0.5%

Eye Lubricant

Soothing

Relief for Dry Eyes

0.5 FL OZ (15 mL)

0.5% bottle label

Principal Display Panel

LEADER®

NDC 70000-0090-1

Sterile

Lubricant

Eye Drops

Carboxymethylcellulose Sodium, 0.5%

Eye Lubricant

Soothing Relief for Dry Eyes

Actual Bottle Size on Side Panel

COMPARE TO REFRESH TEARS® LUBRICANT EYE DROPS active ingredient*

100% Money Back Guarantee

0.5 FL OZ (15 mL)

0.5% carton (1)

Principal Display Panel

LEADER®

NDC 70000-0090-2

Sterile

Lubricant

Eye Drops

Carboxymethylcellulose Sodium, 0.5%

Eye Lubricant

Soothing Relief for Dry Eyes

Actual Bottle Size on Side Panel

COMPARE TO REFRESH TEARS® LUBRICANT EYE DROPS active ingredient*

100% Money Back Guarantee

2 BOTTLES, 0.5 FL OZ (15 mL) each

0.5% carton (2)
LUBRICANT DROPS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0090
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CHLORITE (UNII: G538EBV4VF)  
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID (UNII: QTT17582CB)  
May containSODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70000-0090-11 in 1 CARTON03/09/202111/30/2026
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:70000-0090-22 in 1 CARTON03/09/202111/30/2026
215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01803/09/202111/30/2026
Labeler - CARDINAL HEALTH 110, LLC. DBA LEADER (063997360)

Revised: 9/2025
Document Id: 7032f298-3bfe-4fd2-b240-36ec6015ffbe
Set id: 1ac2fe24-9ff6-48c1-b123-fbc0e48f5304
Version: 4
Effective Time: 20250912
 
CARDINAL HEALTH 110, LLC. DBA LEADER