REFRESH OPTIVE Advanced description, usages, side effects, indications, overdosage, supplying and lots more!

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REFRESH OPTIVE Advanced

Allergan, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Carboxymethylcellulose sodium 0.5%

Glycerin 1%

Polysorbate 80 0.5%

Purpose

Eye lubricant

Eye lubricant

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 59º-86ºF (15º-30ºC).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; carbomer copolymer type A; castor oil; erythritol; levocarnitine; purified water; and sodium hydroxide.

Questions or comments?

1.800.433.8871

refreshbrand.com

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 label Item Code (Source) NDC:0023-4491
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 5 mg
GLYCERIN 10 mg
polysorbate 80 5 mg

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
CARBOMER COPOLYMER TYPE A
castor oil
ERYTHRITOL
LEVOCARNITINE
water
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.4 in 1 VIAL, SINGLE-USE
2 0.4 in 1 VIAL, SINGLE-USE
3 NDC:0023-4491-30 30 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-01-15


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