WALGREENS HYPERTONICITY- sodium chloride ointment

Walgreens Hypertonicity by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient Purpose

Sodium chloride 5%...........................................................Eye hypertonicity agent

PURPOSE

Use

• temporary relief of corneal edema

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

• except under the advice and supervision of a doctor
• if difficult to dispense or visible particles are seen in the product

WHEN USING

When using this product

• it may cause temporary burning and irritation when instilled into the eye
• do not touch tip of container to any surface to avoid contamination
• replace cap after each use
• remove contact lense before using

STOP USE

Stop use and ask a doctor if

• you feel eye pain
• changes in vision occur
• redness or irritation of the eye lasts
• condition worsens or lasts more than 72 hours

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

INDICATIONS & USAGE

Directions

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

STORAGE AND HANDLING

Other information

• store between 15-25°C (59-77°F)
• do not freeze
• keep tightly closed
• do not roll, bend, twist or fold tube during use as this may cause the tube to tear or crack

INACTIVE INGREDIENT

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

DOSAGE & ADMINISTRATION

Distributed by:

200 Wilmot Rd.

Deerfield, IL 60015

Made in South Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS HYPERTONICITY 
sodium chloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1573
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 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1573-01	1 in 1 TUBE	05/15/2018
1		0.125 g in 1 BOX; 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	05/15/2018

Labeler - Walgreen Company (008965063)