CMC Lubricant Eye Drops

Dosage form: solution/ drops
Ingredients: Carboxymethylcellulose Sodium 5mg in 1mL
Labeler: Amerisource Bergen
NDC code: 46122-200

Medically reviewed by Drugs.com. Last updated on Apr 5, 2024.

Drug Facts

Active Ingredient

Carboxymethylcellulose

Sodium 0.5%

Purpose

Lubricant

Uses

For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to the wind and sun.
May be used as a protectant against further irritation.

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
irritation of the eye
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.

Storage

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Other information

Do not use if seal on bottle is missing or broken.
Use before expiration date marked on container.
Retain this carton for future reference.

Inactive Ingredients:

Purified Water, Boric Acid, Sodium Chloride, Potassium Chloride, Calcium Chloride, Magnesium Chloride. May also contain Hydrochloric Acid and/or Sodium Hydroxide to adjust pH;

Preservative:

Chlorine Dioxide 2% solution.

Questions or comments?

1-800-579-8327

Principal Display Panel Text for Container Label:

46122-200-05

Good Neighbor Pharmacy Logo ®

Lubricant

Eye Drops

CMC 0.5% Lubricant Eye Drops

15 mL (0.5 fl oz)

Sterile

Principal Display Panel Text for Carton Label:

46122-200-05

Compare to

Refresh Tears®

active ingredients*

Good Neighbor Pharmacy Logo ®

Lubricant

Eye Drops

CMC 0.5%

Lubricant Eye Drops

Moisturizing Drops

for Dry Eyes

15 mL

(0.5 fl oz)

Sterile

CMC LUBRICANT EYE DROPS
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:46122-200
Route of Administration	OPHTHALMIC	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Carboxymethylcellulose Sodium (Carboxymethylcellulose)	Carboxymethylcellulose Sodium	5 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water
Boric Acid
Sodium Chloride
Potassium Chloride
Calcium Chloride
Magnesium Chloride
Hydrochloric Acid
Sodium Hydroxide
Chlorine Dioxide

Packaging
#	Item Code	Package Description
1	NDC:46122-200-05	1 BOTTLE, DROPPER in 1 CARTON
1		15 mL in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	03/22/2013

Labeler - Amerisource Bergen (007914906)

Registrant - Akorn, Inc. (063434679)

Establishment
Name	Address	ID/FEI	Operations
Akorn, Inc		603980319	MANUFACTURE(46122-200), ANALYSIS(46122-200), STERILIZE(46122-200), PACK(46122-200), LABEL(46122-200)

Revised: 04/2013

Document Id: 393a4319-d7b8-4181-8ea9-5b8f2d4a6a43

Set id: af3bba43-b05e-416d-a34a-bf1029ab13f7

Version: 2

Effective Time: 20130415

Amerisource Bergen

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer