Active ingredients

Carboxymethylcellulose sodium 0.5%

Glycerin 1%

Polysorbate 80 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. Do not reuse. Once opened, discard.
Do not touch unit-dose tip to eye.
If solution changes color, 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

To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

Other information

Use only if single-use container is intact.
Use before expiration date marked on container.
Store at 59°-77°F (15°-25°C).
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; carbomer copolymer type A; castor oil; erythritol; levocarnitine; purified water; and sodium hydroxide (to adjust pH).

Questions or comments?

1.800.678.1605

refreshbrand.com

v1.0DFL4491

PRINCIPAL DISPLAY PANEL

NDC 0023-4491-30

Single Use Containers
Preservative-free

Refresh
Optive®
ADVANCED
Lubricant Eye Drops

TRIPLE-ACTION RELIEF

Clinically proven to lubricate, hydrate,
and protect natural tears from evaporating

30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile

PRINCIPAL DISPLAY PANEL
NDC 0023-4491-30
Single Use Containers
Preservative-free
Refresh
Optive®
ADVANCED
Lubricant Eye Drops
TRIPLE-ACTION RELIEF
Clinically proven to lubricate, hydrate,
and protect natural tears from evaporating
30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile

REFRESH OPTIVE ADVANCED
carboxymethylcellulose sodium, glycerin, polysorbate 80 solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0023-4491
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
glycerin (UNII: PDC6A3C0OX) (glycerin - UNII:PDC6A3C0OX)	glycerin	10 mg in 1 mL
polysorbate 80 (UNII: 6OZP39ZG8H) (polysorbate 80 - UNII:6OZP39ZG8H)	polysorbate 80	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
boric acid (UNII: R57ZHV85D4)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
castor oil (UNII: D5340Y2I9G)
erythritol (UNII: RA96B954X6)
levocarnitine (UNII: 0G389FZZ9M)
water (UNII: 059QF0KO0R)
sodium hydroxide (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0023-4491-05	5 in 1 CARTON	01/15/2013
1		0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2	NDC:0023-4491-30	30 in 1 CARTON	01/15/2013
2		0.4 mL in 1 VIAL, SINGLE-USE; 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	01/15/2013

Labeler - Allergan, Inc. (144796497)