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

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Systane Nighttime

Alcon Laboratories, Inc.
Alcon Laboratories, Inc.

Systane Nighttime Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OTC - ACTIVE INGREDIENT SECTION

Mineral Oil 3%
White Petrolatum 94%

OTC - PURPOSE SECTION

Lubricant

INDICATIONS & USAGE SECTION

  • For use as a lubricant to prevent further irritation or to relieve dryness of the eye.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

  • if you are sensitive to any ingredient in this product

OTC - WHEN USING SECTION

  • remove contact lenses before using
  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using

OTC - STOP USE SECTION AND ASK A DOCTOR IF

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Pull down the lower lid of the affected eye and apply a small amount (one-fourth inch) of ointment to the inside of the eyelid.

OTHER INFORMATION

  • Store at 8°-27°C (46°-80°F).

INACTIVE INGREDIENT SECTION

Anhydrous Liquid Lanolin 3%.

OTC - QUESTIONS SECTION

In the U.S., call 1-800-757-9195 or visit www.systane.com

PRINCIPAL DISPLAY PANEL

FOR NIGHTTIME PROTECTION OF DRY EYES

Systane®
NIGHTTIME
LUBRICANT EYE OINTMENT

OVERNIGHT RELIEF

DRY EYE THERAPY

Systane®
NIGHTTIME
LUBRICANT EYE OINTMENT

Systane® Nighttime Lubricant Eye Ointment is a safe and effective formulation with no preservatives. This unpreserved ointment, when applied to the eyes, forms a smooth comfortable protective film, especially useful for nighttime protection and lubrication of dry eyes.

PRESERVATIVE-FREE

Alcon®
STERILE
3.5 g Tube (1/8 OZ NET WT)

Systane Nighttime

mineral oil and white petrolatum OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0065-0509
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Mineral Oil 30 mg
petrolatum 940 mg

Inactive Ingredients

Ingredient Name Strength
LANOLIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 TUBE
2 NDC:0065-0509-35 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2008-06-26


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