SODIUM CHLORIDE- 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 5%

Purpose

Hypertonicity agent

Use

For temporary relief of corneal edema.

Warnings

Stop use and ask a doctor if

you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep out of the reach of children.

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

Questions or comments? 1-800-932-5676

Directions

Apply small amount (one-fourth inch) to the inside of affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Other information

Inactive ingredients

Mineral Oil, Modified Lanolin, Purified Water and White Petrolatum.

Principal Display Panel Text for Container Label:

CVS Health Logo NDC 59779-303-01

Sodium Chloride USP, 5%

HYPERTONICITY OPHTHALMIC OINTMENT

NET WT 0.125 OZ (3.5 g) STERILE

Principal Display Panel Text for Container Label

Principal Display Panel Text for Carton Label:

CVS Health Logo Compare to the active

ingredient in Muro® 128*

Sodium Chloride, NDC 59779-303-01

USP, 5%

HYPERTONICITY OPHTHALMIC OINTMENT

Temporary relief of corneal edema

NET WT 0.125 OZ (3.5 g) STERILE

Principal Display Panel Text for Carton Label
SODIUM CHLORIDE 
sodium chloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-303
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
Mineral Oil (UNII: T5L8T28FGP)  
Lanolin (UNII: 7EV65EAW6H)  
Water (UNII: 059QF0KO0R)  
Petrolatum (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-303-011 in 1 CARTON02/21/2013
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 finalpart34902/21/2013
Labeler - CVS Pharmacy (062312574)
Registrant - Akorn Operating Company LLC (117693100)
Establishment
NameAddressID/FEIBusiness Operations
Akorn117696840MANUFACTURE(59779-303) , ANALYSIS(59779-303) , STERILIZE(59779-303) , PACK(59779-303) , LABEL(59779-303)

Revised: 1/2022
Document Id: 78c3830d-0e04-4db1-bd04-995a6c66a455
Set id: b610ad5e-7e80-4bce-b61f-da04eb894537
Version: 5
Effective Time: 20220125
 
CVS Pharmacy