MURO 128- sodium chloride ointment 
Bausch & Lomb Incorporated

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.

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Muro 128 Drug Facts

Active ingredient

Sodium chloride 5%

Purpose

Hypertonicity agent

Uses

temporary relief of corneal edema

Warnings

For external use only

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 provided below 

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

Questions or comments?

Call 1-800-553-5340

Package/Label Principal Display Panel

cartonBAUSCH +LOMB

NDC 24208-385-56

Muro 128®

sodium chloride hypertonicity

ophthalmic ointment, 5%

OINTMENT

5%|

Temporary Relief

of Corneal Edema

TWIN

PACK

STERILE

NET WT. 1/4 OZ. (7 g)

TWO 1/8 OZ (3.5 g) Tubes

9758101
AB15899

MURO 128 
sodium chloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-385
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN (UNII: 7EV65EAW6H)  
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
MINERAL OIL (UNII: T5L8T28FGP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24208-385-551 in 1 CARTON01/01/2011
13.5 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:24208-385-562 in 1 CARTON01/01/2011
23.5 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:24208-385-011 in 1 CARTON01/01/2011
31 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34901/01/2011
Labeler - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIBusiness Operations
Bausch & Lomb Incorporated079587625MANUFACTURE(24208-385)

Revised: 4/2022
Document Id: 679c25d1-0010-47a9-9ffb-38c00b037480
Set id: 93fafa27-5031-4d95-b4b8-5574b7204ae2
Version: 8
Effective Time: 20220419
 
Bausch & Lomb Incorporated