REFRESH OPTIVE DROPS- carboxymethylcellulose sodium and glycerin solution/ drops 
Allergan, Inc.

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REFRESH OPTIVE® GEL DROPS
Drug Facts

Active ingredients

Carboxymethylcellulose sodium 1%

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

v1.0DFL5459

PRINCIPAL DISPLAY PANEL

Refresh
Optive
GEL DROPS
Extended Therapy
0.33 fl oz (10 mL)

PRINCIPAL DISPLAY PANEL
Refresh
Optive
GEL DROPS
Extended Therapy
0.33 fl oz (10 mL)

REFRESH OPTIVE DROPS 
carboxymethylcellulose sodium and glycerin solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-5459
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
carboxymethylcellulose sodium (UNII: K679OBS311) (carboxymethylcellulose - UNII:05JZI7B19X) carboxymethylcellulose sodium10 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)  
sodium chlorite (UNII: G538EBV4VF)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-5459-101 in 1 CARTON09/30/2015
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:0023-5459-021 in 1 CARTON09/30/2015
22 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 DrugM01809/30/2015
Labeler - Allergan, Inc. (144796497)

Revised: 7/2022
Document Id: 4fc2d31c-5670-4dc9-9148-b443c423e6a7
Set id: 80275190-d717-40ea-905b-5c8fbe986eac
Version: 9
Effective Time: 20220712
 
Allergan, Inc.