WALGREENS SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE- sodium chloride ointment
Walgreen Company

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Walgreens Sodium Chloride Ophthalmic Ointment 5 Percent Hypertonicity Eye Ointment

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 eyes only.

• 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 doctor if

• 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.

Questions or comments?

•1- 800-925-4733

PRINCIPAL DISPLAY PANEL

NDC 0363-7500-50

Sodium Chloride

Ophthalmic

Ointment, 5%

Hypertonicity

Eye Ointment

NET WT 0.125 OZ (3.5 g)

Carton

Label

WALGREENS SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-7500
Route of Administration	OPHTHALMIC

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-7500-50	1 in 1 CARTON	04/01/2019	12/31/2024
1		3.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M018	04/01/2019	12/31/2024

Labeler - Walgreen Company (008965063)

Revised: 11/2025

Document Id: 43d829b8-e500-39c3-e063-6294a90a31b8

Set id: bda3b9db-5fc4-408c-a5ae-d1eeb3ee308d

Version: 10

Effective Time: 20251117

Walgreen Company