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Muro 128 by Bausch & Lomb Incorporated

Dosage form: solution
Ingredients: SODIUM CHLORIDE 20mg in 1mL
Labeler: Bausch & Lomb Incorporated
NDC Code: 24208-276

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Muro 128

Drug Facts

Active ingredient

Sodium chloride 2%

Purpose

Hypertonicity agent

Uses

temporary relief 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 0.028%, propylparaben 0.012%

Questions?

Call 1-800-323-0000

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

Package/Label Principal Display Panel

Doctor Recommended!

NDC 24208-276-15

Bausch & Lomb

Muro 128®

sodium chloride hypertonicity ophthalmic solution, 2%

2%

STERILE

1/2 FL. OZ. (15mL)

MURO 128 
sodium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-276
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (SODIUM CATION) SODIUM CHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID 
HYPROMELLOSES 
PROPYLENE GLYCOL 
WATER 
SODIUM BORATE 
HYDROCHLORIC ACID 
SODIUM HYDROXIDE 
METHYLPARABEN 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:24208-276-151 BOTTLE in 1 CARTON
115 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/01/2011
Labeler - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIOperations
Bausch & Lomb Incorporated079587625MANUFACTURE(24208-276)

 
Bausch & Lomb Incorporated

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Medically reviewed on Dec 29, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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