Active ingredient

Carboxymethylcellulose sodium 0.5%

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 and/or sodium hydroxide (to adjust pH).

Questions or comments?

1.800.678.1605

refreshbrand.com

v1.0DFL0798

PRINCIPAL DISPLAY PANEL

Refresh
Tears®
Lubricant Eye Drops
ORIGINAL STRENGTH
Moisturizing Relief for
Dry, Irritated Eyes
0.5 fl oz (15 mL) Sterile

PRINCIPAL DISPLAY PANEL

Multi-Pack
More bottles
for more places
Refresh
Tears®
Lubricant Eye Drops
ORIGINAL STRENGTH
Moisturizing Relief for
Dry, Irritated Eyes
4 bottles 0.5 fl oz (15 mL) each
plus 1 bottle 0.17 fl oz (5 mL) Sterile

REFRESH TEARS
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0023-0798
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 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 CHLORITE (UNII: G538EBV4VF)
SODIUM CHLORATE (UNII: T95DR77GMR)
CHLORINE DIOXIDE (UNII: 8061YMS4RM)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0023-0798-04	1 in 1 CARTON	05/16/1997
1		3 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC:0023-0798-03	1 in 1 CARTON	05/16/1997
2		3 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3	NDC:0023-0798-15	1 in 1 CARTON	05/16/1997
3		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
4	NDC:0023-0798-01	2 in 1 CARTON	05/16/1997
4		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
5	NDC:0023-0798-02	4 in 1 CARTON	05/16/1997	01/27/2018
5		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	05/16/1997

REFRESH TEARS
carboxymethylcellulose sodium kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0023-0795

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0023-0795-65	1 in 1 CARTON	01/01/2000
1		1 in 1 TRAY; Type 1: Convenience Kit of Co-Package

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	4 BOTTLE, DROPPER	60 mL in 4
Part 2	1 BOTTLE, DROPPER	5 mL

Part 1 of 2

REFRESH TEARS
carboxymethylcellulose sodium solution/ drops

Product Information
Item Code (Source)	NDC:0023-0796
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 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 CHLORITE (UNII: G538EBV4VF)
SODIUM CHLORATE (UNII: T95DR77GMR)
CHLORINE DIOXIDE (UNII: 8061YMS4RM)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0023-0796-15	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	01/01/2000

Part 2 of 2

REFRESH TEARS
carboxymethylcellulose sodium solution/ drops

Product Information
Item Code (Source)	NDC:0023-0797
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 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 CHLORITE (UNII: G538EBV4VF)
SODIUM CHLORATE (UNII: T95DR77GMR)
CHLORINE DIOXIDE (UNII: 8061YMS4RM)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0023-0797-05	5 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	01/01/2000

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	01/01/2000

Labeler - Allergan, Inc. (144796497)

REFRESH TEARS® Drug Facts

Active ingredient

Purpose

Uses

Warnings

Stop use and ask a doctor if

Keep out of reach of children.

Directions

Other information

Inactive ingredients

Questions or comments?

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

REFRESH TEARS®
Drug Facts