SODIUM CHLORIDE solution/ drops

Sodium Chloride by

Drug Labeling and Warnings

Sodium Chloride by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Walgreen’s 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)

INGREDIENTS AND APPEARANCE

SODIUM CHLORIDE 
sodium chloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0193
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0193-13	1 in 1 BOX	04/01/2019
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	04/01/2019

Labeler - Walgreen Company (008965063)