TheraTears Lubricant description, usages, side effects, indications, overdosage, supplying and lots more!

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TheraTears Lubricant

Advanced Vision Research (Subsidiary of Akorn, Inc.)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Sodium Carboxy-methylcellulose 0.25%

Purpose

Eye lubricant

Uses

  • As a lubricant to relieve dryness of the eye.
  • As a protectant against further irritation of the eye.
  • For temporary relief of burning, irritation, and discomfort including exposure to wind or sun.

Warnings

For external use only

  • To avoid contamination do not touch tip of opened container to any surface. Replace cap after using.

Do not use

  • if solution changes color or becomes cloudy

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness or irritation
  • 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

  • Do not use if Advanced Vision Research neckband is broken or missing.

Inactive ingredients

borate buffers, calcium chloride, Dequest®, magnesium chloride, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium perborate, and sodium phosphate

Principal Display Panel Text for Container Label:

Thera Tears logo

Lubricant Eye Drops

Preservative Free in the Eye

for Maximum Relief

1 FL OZ (30 mL) Sterile

Principal Display Panel Text for Carton Label:

EXTRA VALUE

SIZE

Thera Tears logo

Lubricant Eye Drops

Sterile

Soothing Dry-Eye Relief

that Works!

  • Preservative
    Free in the Eye
    for Maximum
    Relief
  • Replicates
    Human
    Tears

ADVANCED

VISION RESEARCH logo

AN AKORN COMPANY

1FL OZ (30 mL)

TheraTears Lubricant

carboxymethylcellulose sodium SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58790-001
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 2.5 mg

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
SODIUM PERBORATE
calcium chloride
diethylenetriamine pentamethylene phosphonic acid
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM BICARBONATE
SODIUM CHLORIDE
SODIUM PERBORATE
sodium phosphate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE, DROPPER
2 15 in 1 BOTTLE, DROPPER
3 NDC:58790-001-15 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 1999-07-01


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