MURO 128- sodium chloride ointment

Muro 128 by

Drug Labeling and Warnings

Muro 128 by is a Otc medication manufactured, distributed, or labeled by Bausch & Lomb Incorporated. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Sodium chloride, 50 mg (5%)

Purpose

Hypertonicity agent

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

Other information

• store at 15° - 25°C (59° - 77°F)
• keep tightly closed
• DO NOT FREEZE
• see crimp of tube or carton for Lot Number and Expiration Date
• do not use if difficult to dispense or visible particles are seen in the product
• serious side effects associated with use of the product may be reported to the phone number below 

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

Questions?

Call 1-800-323-0000

Package/Label Principal Display Panel

NDC: 24208-385-55

Bausch & Lomb

Muro 128®

sodium chloride hypertonicity ophthalmic ointment, 5%

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

INGREDIENTS AND APPEARANCE

MURO 128 
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24208-385
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24208-385-55	1 in 1 CARTON	01/01/2011
1		3.5 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 24208-385-56	2 in 1 CARTON	01/01/2011
2		3.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/01/2011

Labeler - Bausch & Lomb Incorporated (196603781)

Establishment
Name	Address	ID/FEI	Business Operations
Bausch & Lomb Incorporated		079587625	MANUFACTURE(24208-385)