SODIUM CHLORIDE HYPERTONICITY- sodium chloride ointment 
CVS PHARMACY

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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Drug Facts

Active ingredient

Sodium chloride, 50 mg (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 below

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

Questions

[phone icon] Call 1-866-767-9161

Package/Label Principal Display Panel - Carton

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Compare to the active
ingredient in Muro 128®*

NDC 69842-285-35

Sodium Chloride
Hypertonicity
ophthalmic ointment, 5%
Temporary relief of corneal edema

NET WT 0.125 OZ (3.5 g)

STERILE

carton3.5gointment
SODIUM CHLORIDE HYPERTONICITY 
sodium chloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-285
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)  
MINERAL OIL (UNII: T5L8T28FGP)  
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-285-351 in 1 CARTON05/01/2020
13.5 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/01/2020
Labeler - CVS PHARMACY (062312574)
Establishment
NameAddressID/FEIBusiness Operations
Bausch & Lomb Incorporated079587625MANUFACTURE(69842-285)

Revised: 1/2021
Document Id: 7f3b23e6-ecb8-44b2-9e66-71deb246bc35
Set id: d5cc6cd1-ddf8-4f5b-a021-204cdda0db94
Version: 3
Effective Time: 20210126
 
CVS PHARMACY