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Muro 128 by Bausch & Lomb Incorporated

Dosage form: ointment
Ingredients: SODIUM CHLORIDE 50mg in 1g
Labeler: Bausch & Lomb Incorporated
NDC Code: 24208-385

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 ingredients

Sodium chloride, 50 mg (5%)


Hypertonicity agent


temporary relieve of corneal edema


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.

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
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


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)

MURO 128 
sodium chloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-385
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:24208-385-551 TUBE in 1 CARTON
13.5 g in 1 TUBE
2NDC:24208-385-562 TUBE in 1 CARTON
23.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/01/2011
Labeler - Bausch & Lomb Incorporated (196603781)
Bausch & Lomb Incorporated079587625MANUFACTURE(24208-385)

Revised: 08/2014
Bausch & Lomb Incorporated

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.