Active ingredient

Carboxymethylcellulose sodium 1%

Purpose

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 or becomes cloudy, 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.

Other information

Use only if tape seals on top and bottom flaps are intact.
Use before expiration date marked on container.
Discard 90 days after opening.
Store at 59°-77°F (15°-25°C).
RETAIN THIS CARTON FOR FUTURE REFERENCE.

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
Soothes & Comforts
Dry, Irritated Eyes
0.5 fl oz (15 mL) Sterile

PRINCIPAL DISPLAY PANEL
NDC 0023-9205-15
Refresh
Liquigel®
Lubricant Eye Gel
Soothes & Comforts
Dry, Irritated Eyes
0.5 fl oz (15 mL) Sterile

REFRESH LIQUIGEL
carboxymethylcellulose sodium gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0023-9205
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (Carboxymethylcellulose - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0023-9205-03	1 in 1 CARTON	10/04/2001	04/12/2020
1		3 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC:0023-9205-15	1 in 1 CARTON	10/04/2001
2		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3	NDC:0023-9205-02	2 in 1 CARTON	10/04/2001	04/12/2020
3		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	10/04/2001

Labeler - Allergan, Inc. (144796497)

REFRESH LIQUIGEL® Drug Facts