REFRESH REPAIR PRESERVATIVE-FREE- carboxymethylcellulose sodium and 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 Preservative-free
Lubricant Eye Drops
Drug Facts

Active ingredients

Carboxymethylcellulose sodium 0.5%
Glycerin 0.9%

Purpose

Eye lubricant
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, 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.
  • Prior to first use, bottle must be primed. Please read the “Instructions for Use” on the insert inside this carton.
  • *If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions. 

Other information

  • Use only if tape seals on top and bottom flaps are intact.
  • Use before expiration date marked on container.
  • Store at 59°-86°F (15°-30°C).   
  • RETAIN THIS CARTON AND THE INSERT FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; calcium chloride dihydrate; erythritol; levocarnitine; magnesium chloride hexahydrate; potassium chloride; purified water; sodium borate decahydrate; sodium citrate dihydrate; and sodium hyaluronate. May also contain hydrochloric acid and/or sodium hydroxide to adjust ph.

Questions or comments?

Telephone number and website

HOW SUPPLIED: 0.33 fly oz. (10 ml)                         UPC: 3-0023-6465-10-0
Made in the U.S.A

PRINCIPAL DISPLAY PANEL

Refresh
Repair
Repairs and Protects the
Eye’s Surface; Also Relieves
LASIK Dryness*
NEW!
PRESERVATIVE-FREE
0.33 fl oz. (10 mL) Sterile

Refresh Repair Repairs and Protects the Eye’s Surface; Also Relieves LASIK Dryness* NEW! PRESERVATITVE-FREE 0.33 fl oz (10 mL) Sterile

PRINCIPAL DISPLAY PANEL

Refresh
Repair
Repairs and Protects the
Eye’s Surface; Also Relieves
LASIK Dryness*
NEW!
PRESERVATIVE-FREE
0.33 fl oz. (10 mL) Sterile
PROFESSIONAL SAMPLE
Not for Retail Sale

Refresh Repair Repairs and Protects the Eye’s Surface; Also Relieves LASIK Dryness* NEW! PRESERVATIVE-FREE 0.33 fl oz. (10 mL) Sterile PROFESSIONAL SAMPLE Not for Retail Sale  

REFRESH REPAIR PRESERVATIVE-FREE 
carboxymethylcellulose sodium and glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-6465
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)  
LEVOCARNITINE (UNII: 0G389FZZ9M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
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:0023-6465-101 in 1 CARTON05/02/201902/27/2021
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:0023-6465-111 in 1 CARTON05/02/201902/27/2021
210 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 finalpart34905/02/201902/27/2021
Labeler - Allergan, Inc. (144796497)

Revised: 2/2021
Document Id: 1330e230-584c-4b3e-a62b-785360a6daac
Set id: b982675e-163f-424c-bf6a-e561e78fc131
Version: 2
Effective Time: 20210227
 
Allergan, Inc.