CMC LUBRICANT EYE DROPS- carboxymethylcellulose sodium solution/ drops 
Amerisource Bergen

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.


Drug Facts

Active Ingredient


Sodium 0.5%




  • 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.


  • 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.


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


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;


Chlorine Dioxide 2% solution.

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Eye Drops

CMC 0.5% Lubricant Eye Drops

15 mL (0.5 fl oz)


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active ingredients*

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15 mL

(0.5 fl oz)


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carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-200
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Carboxymethylcellulose Sodium (UNII: K679OBS311) (Carboxymethylcellulose - UNII:05JZI7B19X) Carboxymethylcellulose Sodium5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Boric Acid (UNII: R57ZHV85D4)  
Sodium Chloride (UNII: 451W47IQ8X)  
Potassium Chloride (UNII: 660YQ98I10)  
Calcium Chloride (UNII: M4I0D6VV5M)  
Magnesium Chloride (UNII: 02F3473H9O)  
Hydrochloric Acid (UNII: QTT17582CB)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Chlorine Dioxide (UNII: 8061YMS4RM)  
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-200-051 in 1 CARTON03/22/201301/31/2017
115 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 finalpart34903/22/201301/31/2017
Labeler - Amerisource Bergen (007914906)

Revised: 10/2020
Amerisource Bergen