REFRESH LIQUIGEL- carboxymethylcellulose sodium gel 
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 LIQUIGEL® 
Drug Facts

Active ingredient

Carboxymethylcellulose sodium 1%

Purpose

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

Questions or comments?

Telephone

1.800.687.1605

refreshbrand.com

v1.0DFL9205

PRINCIPAL DISPLAY PANEL

NDC 0023-9205-15

Refresh

Liquigel®

Lubricant Eye Gel

SOOTHING GEL

Long-lasting relief
for dry eyes in a

soothing gel formula

0.5 fl oz (15 mL) Sterile

NDC 0023-9205-15

Refresh
Liquigel®
Lubricant Eye Gel

SOOTHING GEL
Long-lasting relief
for dry eyes in a 
soothing gel formula

0.5 fl oz (15 mL) Sterile

REFRESH LIQUIGEL 
carboxymethylcellulose sodium gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-9205
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Carboxymethylcellulose sodium (UNII: K679OBS311) (Carboxymethylcellulose - UNII:05JZI7B19X) Carboxymethylcellulose sodium10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Boric acid (UNII: R57ZHV85D4)  
calcium chloride (UNII: M4I0D6VV5M)  
magnesium chloride (UNII: 02F3473H9O)  
potassium chloride (UNII: 660YQ98I10)  
water (UNII: 059QF0KO0R)  
sodium borate (UNII: 91MBZ8H3QO)  
sodium chloride (UNII: 451W47IQ8X)  
sodium chlorite (UNII: G538EBV4VF)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-9205-031 in 1 CARTON10/04/200104/12/2020
13 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:0023-9205-151 in 1 CARTON10/04/2001
215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:0023-9205-022 in 1 CARTON10/04/200104/12/2020
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 finalpart34910/04/2001
Labeler - Allergan, Inc. (144796497)

Revised: 11/2022
Document Id: 7a6e5495-f68b-4007-917f-8a40c8404422
Set id: 4b8b2f6a-4b89-446c-9e5b-9b83c453a01d
Version: 7
Effective Time: 20221111
 
Allergan, Inc.