SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE- sodium chloride ointment

Drug Labeling and Warnings

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Walgreens Sodium Chloride Ophthalmic

Ointment 5% Hypertonicity Eye Ointment 3.5g

NDC 0363-7500-50

Drug Facts

Active ingredient

Sodium Chloride, 50 mg (5%)

Purpose

Hypertonicity Agent

Use

For the temporary relief of corneal edema.

Warnings

For use in the eyesonly.

Retain outer carton for full product drug facts.

Do not use

this product except under the advice and supervision of a doctor.

When using this product

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

replace cap after use.

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

Stop use and ask a doctorif

you experience eye pain, changes in vision, continued redness or irritation of the eye.

 condition worsens or persists for more than 72 hours.

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.

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

Directions

pull down lower lid of the affected eye(s) and apply a small amount (1/4 inch) to the inside of the eyelid and apply every 3-4 hours, or as directed by a doctor.

Other information

Store at room temperature 15°- 30°C (59°- 86°F).

Do not freeze.

Keep tightly closed.

See crimp of tube or box for lot number and expiration date.

Inactive ingredients

lanolin alcohol, mineral oil, water for injection and white petrolatum.

Questionsor comments?

1- 800-925-4733

NDC:

0363-7500-50 Sodium Chloride Ophthalmic Ointment, 5% Hypertonicity Eye Ointment NET WT 0.125 OZ (3.5 g)

Tube Label

INGREDIENTS AND APPEARANCE

SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE 
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11716-0750
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11716-0750-0	1 in 1 CARTON	04/04/2026
1		3.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	04/04/2026

Labeler - Hanlim (687986034)