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

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REFRESH PLUS

Allergan, Inc.

REFRESH PLUSLubricant Eye Drops


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

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. Do not reuse. Once opened, discard.
  • Do not touch unit-dose tip to eye.
  • 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

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

*lf used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor's instructions.

Other information

  • Use only if single-use container is intact.
  • Use before expiration date marked on container.
  • Store at 59°-86°F (15°-30°C).
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Calcium chloride; magnesium chloride; potassium chloride; purified water; sodium chloride; and sodium lactate.

May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

Questions or comments?

1.800.433.8871, M-F 6 AM - 4:30 PM Pacific Time

refreshbrand.com

NDC 0023-0403-30

SENSITIVE
Preservative-free

Refresh
Plus
®
Lubricant Eye Drops

Moisture drops for
dry eyes including
LASIK dryness*

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

REFRESH PLUS

carboxymethylcellulose sodium SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0023-0403
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 5 mg

Inactive Ingredients

Ingredient Name Strength
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM CHLORIDE
sodium lactate
HYDROCHLORIC ACID
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 0.4 in 1 VIAL, SINGLE-USE
4 0.4 in 1 VIAL, SINGLE-USE
5 0.4 in 1 VIAL, SINGLE-USE
6 NDC:0023-0403-10 100 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 1996-10-09


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