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

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REFRESH TEARS

Mechanical Servants, Inc.

REFRESH TEARS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

REFRESH TEARS 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.

REFRESH TEARS Other information

  • Use only if imprinted tape seal on bottle is intact and clearly legible.
  • Use before expiration date marked on container.
  • Store at 59°-86°F (15°-30°C).
  • RETAIN THIS CARD FOR FUTURE REFERENCE.

Inactive ingredients

Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate; and sodium chloride. 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

Repackaged and distributed by Convenience Valet®
Melrose Park, IL 60160

PRINCIPAL DISPLAY PANEL - 3 mL Bottle Label

CONVENIENCE
CV
VALET
®

PERSONAL
CARE

Refresh
Tears
®
Lubricant Eye Drops

0.1 fl oz (3 mL) Sterile

REFRESH TEARS

REFRESH TEARS

carboxymethylcellulose sodium SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:29485-1073(NDC:0023-0798)
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
BORIC ACID
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
water
sodium chlorite
SODIUM CHLORATE
chlorine dioxide
SODIUM BORATE
SODIUM CHLORIDE
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3 in 1 BOTTLE, DROPPER
2 NDC:29485-1073-0 1 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-01-01


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Be sure to consult your doctor before taking any medication!
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