SODIUM CHLORIDE- sodium chloride ointment 
Walgreens

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 occur
  • continued redness or irritation of the eye
  • the condition worsens or persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

Questions or comments?

1-800-932-5676

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STERILE Well at

Sodium Chloride Walgreens

Ophthalmic Ointment NDC 0363-9050-00

USP, 5% NET WT 3.5 g (1/8 oz.)

Hypertonicity Eye Ointment

FOR OPHTHALMIC USE ONLY

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STERILE Well at

Walgreens NDC 0363-9050-00

WALGREENS PHARMACIST RECOMMENDED≠

Sodium Chloride

Ophthalmic Ointment

USP, 5%

Hypertonicity Eye Ointment

Compare to Muro 128®

Ointment active ingredient#

NET WT 3.5 g (1/8 OZ)

Principal Display Panel Text for Carton Label
SODIUM CHLORIDE 
sodium chloride ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9050
Route of Administration OPHTHALMIC DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37) Sodium Chloride 50 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
Mineral Oil (UNII: T5L8T28FGP)  
Lanolin (UNII: 7EV65EAW6H)  
Water (UNII: 059QF0KO0R)  
Petrolatum (UNII: 4T6H12BN9U)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0363-9050-00 1 in 1 CARTON
1 3.5 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part349 02/12/2013
Labeler - Walgreens (008965063)
Registrant - Akorn, Inc. (062649876)
Establishment
Name Address ID/FEI Business Operations
Akorn, Inc 603980319 MANUFACTURE(0363-9050) , ANALYSIS(0363-9050) , STERILIZE(0363-9050) , PACK(0363-9050) , LABEL(0363-9050)

Revised: 2/2014
Document Id: 6b786b80-9636-4732-81df-38eb7b56966d
Set id: 72342206-7b82-46e9-95e0-1e1cea8678a3
Version: 4
Effective Time: 20140207
 
Walgreens