LUBRICANT DROPS- carboxymethylcellulose sodium solution/ drops

Lubricant Drops by

Drug Labeling and Warnings

Lubricant Drops by is a Otc medication manufactured, distributed, or labeled by Cardinal Health, 110 dba LEADER. 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.
• ▪ 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)

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)

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

INGREDIENTS AND APPEARANCE

LUBRICANT DROPS 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70000-0090
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Kind	Ingredient Name	Quantity
May contain	HYDROCHLORIC ACID (UNII: QTT17582CB)
May contain	SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70000-0090-1	1 in 1 CARTON	03/09/2021	11/30/2026
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 70000-0090-2	2 in 1 CARTON	03/09/2021	11/30/2026
2		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	03/09/2021	11/30/2026

Labeler - CARDINAL HEALTH 110, LLC. DBA LEADER (063997360)