MURO 128- sodium chloride solution 
Bausch & Lomb Incorporated

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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

When using this product 

Stop use and ask a doctor if

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

 

Inactive ingredients

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

Questions or comments?

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

© 2022 Bausch & Lomb Incorporated or its affiliates

Marketed by:

Bausch & Lomb Americas Inc.

Bridgewater, NJ 08807 USA

9756601

AB15611

Package/Label Principal Display Panel – Muro 128 15 mL

carton5%

BAUSCH + LOMB

NDC 24208-277-15

Muro 128®

sodium chloride hypertonicity

ophthalmic solution, 5%

SOLUTION

5%

Temporary Relief

of Corneal Edema

STERILE

1/2 FL OZ (15 mL)

MURO 128 
sodium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-277
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24208-277-151 in 1 CARTON01/01/2011
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:24208-277-301 in 1 CARTON01/01/201101/01/2020
230 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:24208-277-591 in 1 CARTON01/01/2011
32 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01801/01/2011
Labeler - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIBusiness Operations
Bausch & Lomb Incorporated079587625manufacture(24208-277)

Revised: 9/2024
Document Id: 22f5bb72-03ec-37ef-e063-6394a90a689e
Set id: 454f337e-d897-46de-ab05-1c543a33061c
Version: 8
Effective Time: 20240925
 
Bausch & Lomb Incorporated