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Retaine CMC Lubricant Eye Drops

Dosage form: solution
Ingredients: CARBOXYMETHYLCELLULOSE SODIUM 5mg in 1mL
Labeler: OCuSOFT Inc.
NDC Code: 54799-897

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

Carboxymethylcellulose sodium 0.5%................................. Eye Lubricant

Uses
  • Relieves dryness of the eye.
  • Temporarily relieves discomfort due to minor irritations of the eye or from exposure to wind or sun.
  • As a protectant against further irritation. 

Warnings For use in the eyes only.
Do not use if solution changes color or becomes cloudy.

When using this product
  • do not touch tip of container to any surface to avoid contamination.
  • do not reuse once opened.

Stop use and ask a doctor if
  • you experience eye pain, changes in vision, continued redness or irritation of the eye.
  • the condition worsens or persists for more than 72 hours.

KEEP OUT OF THE REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions
  • To open, TWIST AND PULL TAB TO REMOVE.
  • Instill 1 or 2 drops into affected eye(s) as needed and discard container.

Other Information
  • Use only if printed tamper seals on top and bottom flaps are intact.
  • Use only if twist top of single-dose container is intact.
  • Store between 15º-30ºC (59º-86ºF).

Inactive Ingredients

Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium lactate.  May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.


Questions or comments?

Call (800) 233-5469 M-F 8:30AM-5:00PM CST or visit www.retainebrand.com

Purpose

Eye Lubricant

RETAINE CMC LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54799-897
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE ) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE 
MAGNESIUM CHLORIDE 
POTASSIUM CHLORIDE 
SODIUM CHLORIDE 
SODIUM LACTATE 
WATER 
HYDROCHLORIC ACID 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:54799-897-3030 VIAL, SINGLE-DOSE (VIAL) in 1 CONTAINER
10.4 mL in 1 VIAL, SINGLE-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/01/2011
Labeler - OCuSOFT Inc. (174939207)
Registrant - OCuSOFT Inc. (174939207)

Revised: 02/2011
Document Id: ac103906-7e9b-4582-9159-34a2cca56dad
Set id: 6b40c38e-31f8-4aca-9456-04128e6c2e93
Version: 2
Effective Time: 20110223
 
OCuSOFT Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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