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.

----------

REFRESH OPTIVE

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?

Telephone
1.800.433.8871
refreshbrand.com

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

Carton
REFRESH OPTIVE 
carboxymethylcellulose sodium and glycerin solution/ drops
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0023-3240
Route of Administration OPHTHALMIC DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
carboxymethylcellulose sodium (UNII: K679OBS311) (carboxymethylcellulose - UNII:05JZI7B19X) carboxymethylcellulose sodium 5 mg  in 1 mL
glycerin (UNII: PDC6A3C0OX) (glycerin - UNII:PDC6A3C0OX) glycerin 9 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:0023-3240-03 1 in 1 CARTON
1 3 mL in 1 BOTTLE, DROPPER
2 NDC:0023-3240-15 1 in 1 CARTON
2 15 mL in 1 BOTTLE, DROPPER
3 NDC:0023-3240-01 2 in 1 CARTON
3 15 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part349 09/06/2006
Labeler - Allergan, Inc. (144796497)
Establishment
Name Address ID/FEI Business Operations
Allergan, Inc. 362898611 MANUFACTURE(0023-3240)

Revised: 2/2014
Document Id: 2358c98f-9740-4da7-ba6d-201984584521
Set id: 7f8d88af-fd3b-4138-af61-f24c59ccebd7
Version: 5
Effective Time: 20140227
 
Allergan, Inc.