WALGREENS SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE- sodium chloride ointment 
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 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7500
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7500-501 in 1 CARTON04/01/2019
13.5 g in 1 TUBE; 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: 3/2023
Document Id: f54b327c-f2e3-229e-e053-2995a90ac85c
Set id: bda3b9db-5fc4-408c-a5ae-d1eeb3ee308d
Version: 7
Effective Time: 20230314
 
Walgreen Company