MURO 128- sodium chloride solution

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]

Drug Facts

Active ingredients

Sodium chloride 5%

Purpose

Hypertonicity agent

Uses

temporary relieve of corneal edema

Warnings

Do not use

• except under the advice and supervision of a doctor
• if solution changes color or becomes cloudy

When using this product  

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

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

•   instill 1 or 2 drops in the affected eye(s) every 3 or 4 hours, or as directed by a physician.

Other information

• store upright at 15° - 25°C (59° - 77°F)
• keep tightly closed
• serious side effects associated with use of the product may be reported to the phone number provided below

 

Inactive ingredients

boric acid, hypromellose, propylene glycol, purified water, sodium borate. Hydrochloric acid and/or sodium hydroxide may be added to adjust pH. PRESERVATIVES ADDED: methylparaben 0.023%, propylparaben 0.01%.

Questions?

Call 1-800-323-0000

Muro 128 is a registered trademark of Bausch & Lomb Incorporated or its affiliates.

Bausch + Lomb, a Division of Valeant Pharmaceuticals

North America LLC, Bridgewater, NJ 08807

9081704

AB15611

Package/Label Principal Display Panel – Muro 128 15 mL

NDC: 24208-277-15

BAUSCH + LOMB

Muro 128®

sodium chloride hypertonicity

ophthalmic solution, 5%

5%

STERILE

1/2 FL. OZ. (15 mL)

INGREDIENTS AND APPEARANCE

MURO 128 
sodium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24208-277
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 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24208-277-15	1 in 1 CARTON	01/01/2011
1		15 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 24208-277-30	1 in 1 CARTON	01/01/2011
2		30 mL in 1 BOTTLE; 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(24208-277)