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

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REFRESH OPTIVE

Allergan, Inc.

REFRESH OPTIVE


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Carboxymethylcellulose sodium 0.5%

Glycerin 0.9%

Purpose

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. 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 imprinted tape seals on top and bottom flaps are intact and clearly legible.
  • Use before expiration date marked on container.
  • Store at 59°-86°F (15°-30°C).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; calcium chloride dihydrate; erythritol; levocarnitine; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate decahydrate; and sodium citrate dihydrate.

Questions or comments?

1.800.433.8871
refreshbrand.com

Refresh
Optive
®
Lubricant Eye Drops

LONG-LASTING HYDRATION

Lubricating and hydrating
formula penetrates the
surface to relieve dryness

0.5 fl oz (15 mL) Sterile

REFRESH OPTIVE

carboxymethylcellulose sodium and glycerin SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0023-3240
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 5 mg
GLYCERIN 9 mg

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
calcium chloride
ERYTHRITOL
LEVOCARNITINE
MAGNESIUM CHLORIDE
potassium chloride
water
sodium chlorite
SODIUM CHLORATE
chlorine dioxide
SODIUM BORATE
TRISODIUM CITRATE DIHYDRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3 in 1 BOTTLE, DROPPER
2 15 in 1 BOTTLE, DROPPER
3 15 in 1 BOTTLE, DROPPER
4 NDC:0023-3240-01 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2006-09-06


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Be sure to consult your doctor before taking any medication!
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