Your browser does not support JavaScript! REFRESH TEARS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [ALLERGAN, INC.]
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REFRESH TEARS (carboxymethylcellulose sodium) solution/ drops
[Allergan, Inc.]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph final
NOTE: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 Label Sections

Drug Facts

Active ingredients

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.
  • 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 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.
  • 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; PURITE® (stabilized oxychloro complex); sodium borate; and sodium chloride. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or comments?

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refreshbrand.com

Refresh
Tears
®
Lubricant Eye Drops

Moisture drops
for dry eyes

0.5 fl oz (15 mL) Sterile

Carton
REFRESH TEARS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:0023-0798
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
boric acid 
calcium chloride 
magnesium chloride 
potassium chloride 
water 
sodium chlorite 
sodium chlorate 
chlorine dioxide 
sodium borate 
sodium chloride 
hydrochloric acid 
sodium hydroxide 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-0798-041 in 1 CARTON
13 mL in 1 BOTTLE, DROPPER
2NDC:0023-0798-031 in 1 CARTON
23 mL in 1 BOTTLE, DROPPER
3NDC:0023-0798-151 in 1 CARTON
315 mL in 1 BOTTLE, DROPPER
4NDC:0023-0798-012 in 1 CARTON
415 mL in 1 BOTTLE, DROPPER
5NDC:0023-0798-024 in 1 CARTON
515 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/16/1997
Labeler - Allergan, Inc. (144796497)
Establishment
NameAddressID/FEIBusiness Operations
Allergan, Inc.362898611MANUFACTURE

Revised: 1/2012
 
Allergan, Inc.

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