SODIUM CHLORIDE- sodium chloride solution/ drops 
Walgreen Company

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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Walgreens Sodium Chloride Ophthalmic Solution

Walgreens Sodium Chloride Ophthalmic

 Solution, 5% Hypertonicity Eye Drops 15mL  

NDC 0363-0193-13

Drug Facts

Active ingredient

Sodium Chloride 5%

Purpose

Hypertonicity Agent

Use

• For the temporary relief of corneal edema.

Warnings

For use in the eyes only

Save box for complete information

Do not use 

• except under the advice and supervision of a doctor.

• if solution changes color or becomes cloudy.

When using this product

• keep tightly closed.

• to avoid contamination, do not touch tip of container to any surface.

• replace cap immediately after each use.

• this product may cause temporary burning and irritation on being instilled into the eye.

Stop use and ask a doctor if  

• you experience eye pain. • changes in your vision occur.

• continued redness or irritation of the eye persists.

• condition worsens or persists.

Keep out of reach of children.

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

Directions

• instill 1 or 2 drops in the affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Other information

• replace cap after using and keep tightly closed.

• store at 15° to 30°C (59° to 86°F).

• remove contact lenses before using.

Inactive ingredients

Boric Acid, Hypromellose, Methylparaben, Propylene Glycol, Propylparaben, Sodium Borate, and Water for injection. Sodium Hydroxide and/or Hydrochloric Acid may be added to adjust pH.

Questions?

• 1-800-925-4733  • 9am – 5pm EST Monday - Friday

PRINCIPAL DISPLAY PANEL

Walgreens

NDC 0363-0193-13

Sodium Chloride

Ophthalmic

Solution, 5%

Hypertonicity

Eye Drops

0.5 FL OZ (15 mL)

CartonLabel

CartonLabel

SODIUM CHLORIDE 
sodium chloride solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0193
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)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0193-131 in 1 BOX04/01/2019
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34904/01/2019
Labeler - Walgreen Company (008965063)

Revised: 5/2023
Document Id: faeb782d-9560-7324-e053-6394a90a22bf
Set id: d112a344-33cc-41d3-bae6-492631ebdba7
Version: 6
Effective Time: 20230505
 
Walgreen Company