REFRESH TEARS- carboxymethylcellulose sodium solution/ drops 
Allergan, Inc.

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REFRESH TEARS®
Drug Facts

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.
  • 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 tape seals on top and bottom flaps are intact.
  • Use before expiration date marked on container.
  • Discard 90 days after opening.
  • Store at 59°-77°F (15°-25°C).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate decahydrate; and sodium chloride. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).

Questions or comments?

1.800.678.1605

refreshbrand.com

v1.0DFL0798

PRINCIPAL DISPLAY PANEL

Refresh
Tears®
Lubricating Eye Drops
MOISTURIZING RELIEF
Immediate, soothing
relief for dry eyes
0.5 fl oz (15 mL) Sterile

Refresh Tears® Lubricating Eye Drops MOISTURIZING RELIEF Immediate, soothing relief for dry eyes 0.5 fl oz (15 mL) Sterile

REFRESH TEARS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-0798
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
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORITE (UNII: G538EBV4VF)  
SODIUM CHLORATE (UNII: T95DR77GMR)  
CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-0798-041 in 1 CARTON05/16/1997
13 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:0023-0798-031 in 1 CARTON05/16/1997
23 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:0023-0798-151 in 1 CARTON05/16/1997
315 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4NDC:0023-0798-012 in 1 CARTON05/16/1997
415 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
5NDC:0023-0798-024 in 1 CARTON05/16/1997
515 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 DrugM01805/16/1997
Labeler - Allergan, Inc. (144796497)

Revised: 6/2022
Document Id: 1d652c12-69fc-4cfb-9d62-c43b2407621d
Set id: 329d1fe0-4432-4565-b7b1-65666bd86526
Version: 7
Effective Time: 20220630
 
Allergan, Inc.