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

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HypoTears

Novartis Pharmaceutical Corporation

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OTC - ACTIVE INGREDIENT SECTION

Polyvinyl alcohol (1%)
Polyethylene glycol 400 (1%)

OTC - PURPOSE SECTION

Lubricant

INDICATIONS & USAGE SECTION

  • For use as a lubricant to relieve dryness of the eye.
  • Temporarily relieves burning and irritation due to dryness of the eye or from exposure to wind or sun.
  • Helps protect against further eye irritation.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

  • if solution changes colors or becomes cloudy
  • if you are allergic to any ingredients

OTC - WHEN USING SECTION

When using this product do not touch tip of container to any surface to avoid contamination.
Replace cap after using.

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience any of the following:

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye
  • condiiton worsens or persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of the reach of children. If swallowed get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions Put 1 or 2 drops in the affected eye(s) as needed.

OTHER SAFETY INFORMATION

Store between 15°-25°C (59°-77°F).

INACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1 mg/mL (preservative), dextrose, edetate disodium, and purified water. May contain hydrochloric acid and/or sodium hydroxide to adjut pH.

OTC - QUESTIONS SECTION

In the U.S. call toll-free
1-866-393-6336;
MedInfo@AlconLabs.com.
Serious side effects associated with use of this product may be reported to this number.

PRINCIPAL DISPLAY PANEL

STERILE
NDC 0078-0519-24

HypoTears®
Lubricant Eye Drops

"Comforting Care for Dry Eye"

15 mL (0.5 fl oz)

Alcon®

HypoTears

polyvinyl alcohol and polyehtylene glycol 400 SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0078-0519
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POLYVINYL ALCOHOL 10 mg
polyethylene glycol 400 Polyethylene Glycol 400 10 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
DEXTROSE
EDETATE DISODIUM
water
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:0078-0519-24 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2005-07-01


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Be sure to consult your doctor before taking any medication!
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