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

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.

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REFRESH TEARS®
Lubricant Eye Drops
Drug Facts

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

Uses

Warnings

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

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?

1.800.433.8871

refreshbrand.com

PRINCIPAL DISPLAY PANEL

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

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 
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 FINALpart34905/16/1997
Labeler - Allergan, Inc. (144796497)
Establishment
NameAddressID/FEIBusiness Operations
Allergan Sales, LLC362898611MANUFACTURE(0023-0798)

Revised: 3/2018
Document Id: 33c6eae6-5bec-4161-bb81-0627aa2df72c
Set id: 329d1fe0-4432-4565-b7b1-65666bd86526
Version: 4
Effective Time: 20180302
 
Allergan, Inc.