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Muro 128

Bausch & Lomb Incorporated

Muro 128 Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Sodium chloride, 50 mg (5%)

Purpose

Hypertonicity agent

Muro 128 Uses

temporary relieve of corneal edema

Warnings

Do not use except under the advice and supervision of a doctor

When using this product  

  • •it may cause temporary burning and irritation
  • •replace cap after use
  • •to avoid contamination do not touch tip of container to any surface

Stop use and ask a doctor if

  • •condition worsens or persists for more than 72 hours
  • •you experience eye pain, changes in vision, continued redness or irritation of the eye

Keep out of reach of children.

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

Directions

  •  pull down the lower lid of the affected eye
  •  apply a small amount (1/4 inch) of ointment to the inside of eyelid
  •  apply every 3 or 4 hours or as directed by a doctor

Muro 128 Other information

  • •store at 15° - 30°C (59° - 86°F)
  • •keep tightly closed
  • •do not freeze
  • •see crimp of tube or carton for Lot Number and Expiration Date
  • •serious side effects associated with use of the product may be reported to the phone number below

 

Inactive ingredient

lanolin, mineral oil, purified water, white petrolatum

Questions?

Call 1-800-323-0000

DO NOT ROLL, BEND, TWIST OR FOLD THE TUBE DURING USE AS THIS MAY CAUSE THE TUBE TO TEAR OR CRACK.

DO NOT USE IF BOTTOM RIDGE OF TUBE CAP IS EXPOSED AND IMPRINTED SEAL ON BOX IS BROKEN OR MISSING.

Bausch & Lomb Incorporated

Tampa, FL 33637

Muro 128 is a registered tradmark of Bausch & Lomb Incorporated

Package/Label Principal Display Panel

NDC 24208-385-55

Doctor Recommended!

Bausch & Lomb

Muro 128®

sodium chloride hypertonicity ophthalmic ointment, 5%

STERILE Net Wt. 1/8 OZ. (3.5 g)

Muro 128

sodium chloride OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24208-385
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE 50 mg

Inactive Ingredients

Ingredient Name Strength
LANOLIN
water
petrolatum
Mineral Oil

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 TUBE
2 3.5 in 1 TUBE
3 NDC:24208-385-56 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-01-01


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Be sure to consult your doctor before taking any medication!
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