REFRESH REPAIR- carboxymethylcellulose sodium, glycerin 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 REPAIR
Lubricant Eye Drops
Drug Facts

Active ingredients

Carboxymethylcellulose sodium 0.5%

Glycerin 0.9%

Purpose

Eye lubricant

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

Questions or comments?

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PRINCIPAL DISPLAY PANEL

NEW
Refresh®
REPAIR
Lubrica
nt Eye Drops
Repairs and Protects
the Eye’s Surface
0.33 fl oz (10 mL) Sterile

PRINCIPAL DISPLAY PANEL
NEW
Refresh®
REPAIR
Lubricant Eye Drops
Repairs and Protects
the Eye’s Surface
0.33 fl oz (10 mL) Sterile

REFRESH REPAIR 
carboxymethylcellulose sodium, glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-4607
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN9 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
ERYTHRITOL (UNII: RA96B954X6)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORITE (UNII: G538EBV4VF)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-4607-101 in 1 CARTON05/21/2018
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:0023-4607-041 in 1 CARTON05/21/2018
23 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 FINALpart34905/21/2018
Labeler - Allergan, Inc. (144796497)

Revised: 2/2019
Document Id: 3f5f656c-8f18-484e-a724-e8fcdeb5f26a
Set id: c4832e66-fed0-4b88-a060-e2a6b6158369
Version: 5
Effective Time: 20190228
 
Allergan, Inc.