REFRESH OPTIVE- 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 OPTIVE® 
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; levocarnitine; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate decahydrate; and sodium citrate dihydrate.

Questions or comments?

1.800.678.1605

refreshbrand.com

PRINCIPAL DISPLAY PANEL

Refresh
Optive
Lubricant Eye Drops
LONG-LASTING HYDRATION
Lubricating and hydrating
formula penetrates the
surface to relieve dryness
0.5 fl oz (15 mL) Sterile

PRINCIPAL DISPLAY PANEL
Refresh
Optive
Lubricant Eye Drops
LONG-LASTING HYDRATION
Lubricating and hydrating
formula penetrates the
surface to relieve dryness
0.5 fl oz (15 mL) Sterile

REFRESH OPTIVE 
carboxymethylcellulose sodium and glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-3240
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 CHLORITE (UNII: G538EBV4VF)  
SODIUM CHLORATE (UNII: T95DR77GMR)  
CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-3240-031 in 1 CARTON09/06/2006
13 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:0023-3240-151 in 1 CARTON09/06/2006
215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:0023-3240-012 in 1 CARTON09/06/2006
315 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 FINALpart34909/06/2006
Labeler - Allergan, Inc. (144796497)
Establishment
NameAddressID/FEIBusiness Operations
Allergan Sales, LLC362898611MANUFACTURE(0023-3240)

Revised: 3/2018
Document Id: 6d64b3d9-69c2-41d5-9a67-159d4725fe45
Set id: 7f8d88af-fd3b-4138-af61-f24c59ccebd7
Version: 9
Effective Time: 20180302
 
Allergan, Inc.